August 2011 - Physical Therapy Journal
Transcription
August 2011 - Physical Therapy Journal
August 2011 Volume 91 Number 8 Research Reports 1153 Age-Related Muscle Fatigue: A Meta-Analysis 1235 1166 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Frontal-Plane Gait Mechanics in Knee Osteoarthritis 1244 Physical Performance Tests and Hemodialysis 1253 Fear of Falling Avoidance Behavior Questionnaire 1184 Cervical Flexor Activity and Temporomandibular Disorders 1198 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment 1211 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective 1223 Association of Body Mass Index With Measures of Balance and Mobility Case Report 1266 Internal Carotid Artery Dissection ProfessionWatch 1275 Outcomes of a Conference to Enhance the Delivery of Care © 2011, HOMER TLC, Inc. All rights reserved. For safer bathrooms at more affordable prices, point your patients’ caregivers to the bath aisle at The Home Depot. With a full selection of ADA-approved solutions, we have what they need. For less. That’s the power of The Home Depot. ® Learn more at homedepot.com/bathsafety THD110211 PTJ 7_2x4_8.indd 1 ® 4/4/11 11:57 AM Physical Therapy Journal of the American Physical Therapy Association ■ Volume 91 ■ Number 8 ■ August 2011 Editorial 1150 Establishing Real Global Connections / Rebecca L. Craik Research Reports Winslow Homer (American, 1836–1910). Eagle Head, Manchester, Massachusetts (High Tide). 1870. Gift of Mrs. William F. Milton, 1923. Photo Credit: Image copyright © The Metropolitan Museum of Art, New York, NY / Art Resource, NY. In a painting that some art critics call “disquieting,” 3 bathers who have just emerged from the ocean bend forward to dry off, remove a shoe, shake out sand. Thoracic spines, elbows, hips, and knees are all flexed to varying degrees. Although the girls are in close physical proximity and— as a composition—are joined together, they seem isolated. They face in opposite directions, with their backs to each other, and 2 of the faces are obscured. Even the dog seems wary. One of the bathers wrings out her wool bathing dress before wringing out her hair. 1153 Age-Related Differences in Muscle Fatigue Vary by Contraction Type: A Meta-analysis / Keith G. Avin, Laura A. Frey Law 1166 Effects of Vestibular Rehabilitation on Multiple Sclerosis– Related Fatigue and Upright Postural Control: A Randomized Controlled Trial / Jeffrey R. Hebert, John R. Corboy, Mark M. Manago, Margaret Schenkman 1184 Electromyographic Activity of the Cervical Flexor Muscles in Patients With Temporomandibular Disorders While Performing the Craniocervical Flexion Test: A CrossSectional Study / Susan Armijo-Olivo, Rony Silvestre, Jorge Fuentes, Bruno R. da Costa, Inae C. Gadotti, Sharon Warren, Paul W. Major, Norman M.R. Thie, David J. Magee 1198 Associations Between Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment: Gait Speed and the Timed “Up & Go” Test / Ellen L. McGough, Valerie E. Kelly, Rebecca G. Logsdon, Susan M. McCurry, Barbara B. Cochrane, Joyce M. Engel, Linda Teri 1208 Invited Commentary / Teresa Y. Liu-Ambrose 1210 Author Response / Ellen L. McGough, Valerie E. Kelly, Rebecca G. Logsdon, Susan M. McCurry, Barbara B. Cochrane, Joyce M. Engel, Linda Teri 1211 Content Validity of the Extended ICF Core Set for Stroke: An International Delphi Survey of Physical Therapists / Andrea Glässel, Inge Kirchberger, Barbara Kollerits, Edda Amann, Alarcos Cieza 1146 ■ Physical Therapy Volume 91 Number 8 August 2011 1223 1235 Association of Body Mass Index With Self-Report and Performance-Based Measures of Balance and Mobility / Departments Andrea L. Hergenroeder, David M. Wert, Elizabeth S. Hile, Stephanie A. Studenski, Jennifer S. Brach 1152 The Bottom Line 1285 Scholarships, Fellowships, and Grants Frontal-Plane Gait Mechanics in People With Medial Knee Osteoarthritis Are Different From Those in People With Lateral Knee Osteoarthritis / Robert J. Butler, Joaquin A. Barrios, Todd Royer, Irene S. Davis 1244 Test-Retest Reliability and Minimal Detectable Change Scores for Sit-to-Stand-to-Sit Tests, the Six-Minute Walk Test, the One-Leg Heel-Rise Test, and Handgrip Strength in People Undergoing Hemodialysis / Eva Segura-Ortí, News from the Foundation for Physical Therapy 1287 Product Highlights 1288 Ad Index Francisco José Martínez-Olmos 1253 Development of a Scale to Assess Avoidance Behavior Due to a Fear of Falling: The Fear of Falling Avoidance Behavior Questionnaire / Merrill R. Landers, Cortney Durand, D. Shalom Powell, Leland E. Dibble, Daniel L. Young Case Report 1266 A Patient With Internal Carotid Artery Dissection / Gilbert M. Willett, Neal A. Wachholtz ProfessionWatch 1275 Vitalizing Practice Through Research and Research Through Practice: The Outcomes of a Conference to Enhance the Delivery of Care / Marc S. Goldstein, David A. Scalzitti, Joanell A. Bohmert, Gerard P. Brennan, Rebecca L. Craik, Anthony Delitto, Edelle C. Field-Fote, Charles Magistro, Christopher M. Powers, Richard K. Shields Visit ptjournal.apta.org To read online Invited Commentaries and Author Responses. View videoclips. Listen to discussion podcasts. August 2011 Volume 91 Number 8 Physical Therapy ■ 1147 Physical Therapy Journal of the American Physical Therapy Association Editorial Office Editor in Chief Managing Editor / Associate Director of Publications: Jan P. Reynolds, [email protected] Rebecca L. Craik, PT, PhD, FAPTA, Philadelphia, PA [email protected] PTJ Online Editor / Assistant Managing Editor: Steven Glaros Deputy Editor in Chief Associate Editor: Stephen Brooks, ELS Editor in Chief Emeritus Production Manager: Liz Haberkorn Manuscripts Coordinator: Karen Darley Permissions / Reprint Coordinator: Michele Tillson Advertising Manager: Julie Hilgenberg Art Director: Barbara Cross Director of Publications: Lois Douthitt APTA Executive Staff Vice President for Communications: Felicity Feather Clancy Chief Financial Officer: Rob Batarla Chief Executive Officer: John D. Barnes Advertising Sales Ad Marketing Group, Inc 2200 Wilson Blvd, Suite 102-333 Arlington, VA 22201 703/243-9046, ext 102 President / Advertising Account Manager: Jane Dees Richardson Board of Directors Daniel L. Riddle, PT, PhD, FAPTA, Richmond, VA Jules M. Rothstein, PT, PhD, FAPTA (1947–2005) Steering Committee Anthony Delitto, PT, PhD, FAPTA (Chair), Pittsburgh, PA; J. Haxby Abbott, PhD, MScPT, DipGrad, FNZCP, Dunedin, New Zealand; Joanell Bohmert, PT, MS, Mahtomedi, MN; Alan M. Jette, PT, PhD, FAPTA, Boston, MA; Charles Magistro, PT, FAPTA, Claremont, CA; Ruth B. Purtilo, PT, PhD, FAPTA, Boston, MA; Julie Whitman, PT, DSc, OCS, Westminster, CO Editorial Board Rachelle Buchbinder, MBBS(Hons), MSc, PhD, FRACP, Malvern, Victoria, Australia; W. Todd Cade, PT, PhD, St Louis, MO; James R. Carey, PT, PhD, Minneapolis, MN; John Childs, PT, PhD, Schertz, TX; Joshua Cleland, PT, DPT, PhD, OCS, FAAOMPT, Concord, NH; Janice J. Eng, PT/OT, PhD, Vancouver, BC, Canada; G. Kelley Fitzgerald, PT, PhD, FAPTA, Pittsburgh, PA; James C. (Cole) Galloway, PT, PhD, Newark, DE; Steven Z. George, PT, PhD, Gainesville, FL; Kathleen Gill-Body, PT, DPT, NCS, Boston, MA; Paul J.M. Helders, PT, PhD, PCS, Utrecht, The Netherlands; Rana Shane Hinman, PT, PhD, Melbourne, Victoria, Australia; Maura D. Iversen, PT, DPT, ScD, MPH, Boston, MA; Diane U. Jette, PT, DSc, Burlington, VT; Christopher Maher, PT, PhD, Lidcombe, NSW, Australia; Chris J. Main, PhD, FBPsS, Keele, United Kingdom; Kathleen Kline Mangione, PT, PhD, GCS, Philadelphia, PA; Sarah Westcott McCoy, PT, PhD, Seattle, WA; Patricia J. Ohtake, PT, PhD, Buffalo, NY; Carolynn Patten, PT, PhD, Gainesville, FL; Linda Resnik, PT, PhD, OCS, Providence, RI; Kathleen Sluka, PT, PhD, Iowa City, IA; Nicholas Stergiou, PhD, Omaha, NE Statistical Consultants Steven E. Hanna, PhD, Hamilton, Ont, Canada; John E. Hewett, PhD, Columbia, MO; Hang Lee, PhD, Boston, MA; Xiangrong Kong, PhD, Baltimore, MD; Michael E. Robinson, PhD, Gainesville, FL; Paul Stratford, PT, MSc, Hamilton, Ont, Canada; David Thompson, PT, PhD, Oklahoma City, OK; Samuel Wu, PhD, Gainesville, FL President: R. Scott Ward, PT, PhD Committee on Health Policy and Ethics Vice President: Paul A. Rockar Jr, PT, DPT, MS Linda Resnik, PT, PhD, OCS (Chair), Providence, RI; Janet Freburger, PT, PhD, Chapel Hill, NC; Alan M. Jette, PT, PhD, FAPTA, Boston, MA; Michael Johnson, PT, PhD, OCS, Philadelphia, PA; Justin Moore, PT, DPT, Alexandria, VA; Ruth B. Purtilo, PT, PhD, FAPTA, Boston, MA Secretary: Laurita M. Hack, PT, DPT, MBA, PhD, FAPTA Treasurer: Elmer Platz, PT Speaker of the House: Shawne E. Soper, PT, DPT, MBA Vice Speaker of the House: William F. McGehee, PT, MHS Directors: Sharon L. Dunn, PT, PhD, OCS; Jennifer E. Green-Wilson, PT, MBA, EdD; Roger A. Herr, PT, MPA, COS-C; Dianne V. Jewell, PT, DPT, PhD, CCS, FAACVPR; Aimee B. Klein, PT, DPT, DSc, OCS; Kathleen K. Mairella, PT, DPT, MA; Dave Pariser, PT, PhD; Mary C. Sinnott, PT, DPT, MEd; Nicole L. Stout, PT, MPT, CLT-LANA 1148 ■ Physical Therapy Volume 91 Number 8 Masthead_8.11.indd 1148 <LEAP> Linking Evidence And Practice Advisory Group Rachelle Buchbinder, MBBS(Hons), MSc, PhD, FRACP, Malvern, Victoria, Australia (Co-Chair); Diane U. Jette, PT, DSc, Burlington, VT (Co-Chair); W. Todd Cade, PT, PhD, St Louis, MO; Christopher Maher, PT, PhD, Lidcombe, NSW, Australia; Kathleen Kline Mangione, PT, PhD, GCS, Philadelphia, PA; David Scalzitti, PT, PhD, OCS, Alexandria, VA August 2011 7/8/11 1:19 PM Subscriptions Physical Therapy (PTJ) (ISSN 00319023) is published monthly by the American Physical Therapy Association (APTA), 1111 North Fairfax Street, Alexandria, VA 22314-1488, at an annual subscription rate of $12 for members, included in dues. Nonmember rates are as follows: Individual (inside USA)—$99; individual (outside USA)— $119 surface mail, $179 air mail. Institutional (inside USA)—$139; institutional (outside USA)—$159 surface mail, $219 air mail. Periodical postage is paid at Alexandria, VA, and at additional mailing offices. Postmaster: Send address changes to Physical Therapy, 1111 North Fairfax Street, Alexandria, VA 22314-1488. Single copies: $15 USA, $15 outside USA. All orders payable in US currency. 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Volume 91 Number 8 Physical Therapy ■ 1149 7/8/11 1:20 PM Editorial Establishing Real Global Connections W hen I typed “global connections” as a search term in Google, I got 52,900,000 results (July 6, 2011). Even an inquiry in Google Scholar yielded 1,390,000 results. It’s rare for undergraduate students not to have some sort of international experience, and many physical therapist professional education programs in the United States send students for an international service learning experience. But the larger meaning of global connections for the physical therapy community and our potential impact on promoting world health became crystal clear at the 16th International World Confederation for Physical Therapy Congress (WCPT) in Amsterdam, the Netherlands, in June. At last count, about 5,300 clinicians traveled from 115 countries for this event. I was struck by the fact that speakers emphasized principles for intervention rather than clinical context (eg, acute care facility, rehabilitation setting). Two of the focused symposia—one related to recovery from stroke, and another on spinal manipulation— exemplify this. The symposium titled “Increasing Practice After Stroke to Optimize Rehabilitation” emphasized using the evidence that supports a relationship between “dose” of task-specific practice and patient outcome. Rather than focusing solely on the advances in technology that expedite practice, the speakers highlighted the need to increase practice time and discussed strategies to overcome barriers such as lack of access to treadmills and robots that facilitate practice. There were discussions about increasing the number of therapists, training others in the community, and helping family members increase the dose. The principle of increased intensity was the message, not the tool. Similarly, the session titled “Spinal Manipulation—Evidence for Physiotherapist Delivery of Effective Procedures” discussed current evidence related to the effectiveness of techniques for cervicogenic headache and low back pain. Although the speakers all agreed that there is a need for additional evidence, they focused on the need to teach effective screening procedures to enhance safe practice in entry-level programs as well as to enhance the skills of practicing clinicians worldwide. I also was impressed with the number of investigators who are conducting research internationally and how comfortable the presenters were with reporting research outcomes using the International Classification of Functioning, Disability and Health (ICF).1 To comment, submit a Rapid Response to this editorial posted online at ptjournal.apta.org. A number of group networking sessions took place based on requests from physical therapists around the world, with topics including animal physical therapy, cardiorespiratory physical therapy, electrophysical agents, and education. These sessions provided an informal opportunity to meet and talk with colleagues who share a common interest. WCPT (www.wcpt.org) currently has subgroups for acupuncture, older people, manual therapy, sports physiotherapy, women’s health, pedatrics, and private practitioners. In addition, WCPT collaborates with various other physical therapy organizations that are not official subgroups. It’s an incredible experience to sit with clinicians, educators, and researchers from around the world and share experiences. Barriers encountered by physical therapists in one country have sometimes been solved by clinicians in other countries. 1150 ■ Physical Therapy Volume 91 Number 8 editorial_8.11.indd 1150 August 2011 7/18/11 10:58 AM Editorial Several discussion panels addressed issues beyond practice, including: • Managing the research challenges of the 21st century • Using physical therapy projects to bring long-term sustainable benefits in conflict zones and disaster areas • Working as an international profession to change health policy and service provision • Addressing factors that affect equitable access to physical therapy in all parts of the world In closing, I congratulate Stanley Paris, PT, PhD, FAPTA, who received the Mildred O. Elson Award, WCPT’s highest honor. In his acceptance speech, he noted, “What I’ve learned over the years is that the gap between nations in terms of practice standards is narrowing.” This seems to be the perfect segue to emphasize the need to break down country “silos” even further. Physical therapists around the world share a common mission: to improve health and function through education, research, and practice. Imagine what would happen if we all worked together in a truly concerted effort to accomplish this goal: • Could our individual organization-led efforts to develop clinical practice guidelines be more successful if we partnered with international groups? (See the ProfessionWatch article by Van der Wees et al.2) • Is there an international template for clinical competency of the new graduate? • Could international research on hot topics such as exercise dose protocols and treatment effectiveness facilitate translation to practice guidelines more efficiently? Let’s work to grow the exciting global connections that we’ve begun to establish. Rebecca L. Craik R.L. Craik, PT, PhD, FAPTA, is Editor in Chief of PTJ and Professor and Chair, Department of Physical Therapy, Arcadia University, Glenside, Pennsylvania. Dr Craik can be reached at: [email protected]. References 1 International Classification of Functioning, Disability and Health: ICF. Geneva, Switzerland: World Health Organization; 2001. 2 Van der Wees PJ, Moore AP, Powers CM, et al. Development of clinical guidelines in physical therapy: perspective for international collaboration [published online ahead of print July 28, 2011]. Phys Ther. doi: 10.2522/ptj.20100305. [DOI: 10.2522/ptj.2011.91.8.1150] August 2011 editorial_8.11.indd 1151 Volume 91 Number 8 Physical Therapy ■ 1151 7/18/11 10:57 AM The Bottom Line The Bottom Line summarizes the key points of articles that report research with a direct impact on patient care. Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control People with multiple sclerosis (MS) have a multitude of symptoms. Fatigue is the most common complaint, followed by impaired mobility. Balance training is an effective treatment for patients with MS who have impaired upright postural control (ie, balance); however, the evidence for the effectiveness of interventions for MSrelated fatigue is limited and inconsistent. Previously, no studies have investigated the effectiveness of a vestibular rehabilitation program on both MS-related fatigue and balance. This study provides early evidence of the feasibility and effectiveness of a vestibular rehabilitation program on fatigue, balance, and disability due to dizziness or disequilibrium for people with MS. Message for patients: If you have MS and have fatigue and balance problems, participation in a program of vestibular rehabilitation may improve fatigue and balance and reduce disability related to dizziness or disequilibrium, with no known side effects. Larger follow-up studies are needed, however, to support these results. See page 1166. Cervical Flexor Activity and Temporomandibular Disorders Cervical spine dysfunction has been reported to be associated with temporomandibular disorders (TMD). Temporomandibular disorders also are commonly associated with other symptoms affecting the head and neck region such as headache, earrelated symptoms, and altered head and cervical posture. However, no study has investigated the presence of cervical muscle impairments using electromyography. The results of this study may give clinicians insight into the importance of the evaluation and possible treatment of the deep neck flexors in patients with TMD. However, randomized clinical trials are necessary to determine the effectiveness of an exercise program targeting the deep neck flexors in these patients. Message for patients: If you have a TMD, these findings may help your physical therapist evaluate your condition. This evaluation would include an examination of the cervical musculature as well as the TMD. See page 1184. Frontal-Plane Gait Mechanics in Knee Osteoarthritis Patients with medial and lateral knee osteoarthritis exhibit different hip and knee mechanics during gait. These differences in mechanics have previously been associated with elevated disease progression. The findings from this study suggest that patients with medial and lateral knee osteoarthritis also have different mechanics at the ankle. The observed differences in mechanics are contrary to current clinical beliefs. The difference in presentation may be due to the chronic effects of the disease process. Message for patients: If you have osteoarthritis on the inside of the knee (medial knee osteoarthritis), the treatments you receive may be different from the treatments that patients with knee osteoarthritis on the outside of the knee (lateral knee osteoarthritis) may receive. See page 1235. Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment Older adults with mild cognitive impairment (MCI) are at higher risk for dementia and associated disability. Functional decline often is accelerated in the presence of both physical and cognitive impairments. In this study of sedentary older adults with amnestic MCI (memory loss), slower physical performance on gait and mobility tasks was associated with lower performance on executive function tasks, such as those involving planning and judgment. Message for patients and families: Comprehensive prevention and rehabilitation strategies that enhance both cognitive and physical function are important in reducing functional decline and disability in older adults. See page 1198. 1152 ■ Physical Therapy Volume 91 Number 8 August 2011 Research Report Age-Related Differences in Muscle Fatigue Vary by Contraction Type: A Meta-analysis Keith G. Avin, Laura A. Frey Law Background. During senescence, despite the loss of strength (force-generating capability) associated with sarcopenia, muscle endurance may improve for isometric contractions. Purpose. The purpose of this study was to perform a systematic meta-analysis of young versus older adults, considering likely moderators (ie, contraction type, joint, sex, activity level, and task intensity). Data Sources. A 2-stage systematic review identified potential studies from PubMed, CINAHL, PEDro, EBSCOhost: ERIC, EBSCOhost: Sportdiscus, and The Cochrane Library. Study Selection. Studies reporting fatigue tasks (voluntary activation) performed at a relative intensity in both young (18 – 45 years of age) and old (ⱖ55 years of age) adults who were healthy were considered. Data Extraction. Sample size, mean and variance outcome data (ie, fatigue index or endurance time), joint, contraction type, task intensity (percentage of maximum), sex, and activity levels were extracted. Data Synthesis. Effect sizes were (1) computed for all data points; (2) sub- K.G. Avin, PT, DPT, Graduate Program in Physical Therapy & Rehabilitation Science, The University of Iowa, Iowa City, Iowa. L.A. Frey Law, PT, PhD, Graduate Program in Physical Therapy & Rehabilitation Science, The University of Iowa, 1-252 Medical Education Bldg, Iowa City, IA 52242-1190 (USA). Address all correspondence to Dr Frey Law at: [email protected]. [Avin KG, Frey Law LA. Age-related differences in muscle fatigue vary by contraction type: a metaanalysis. Phys Ther. 2011;91: 1153–1165.] © 2011 American Physical Therapy Association Published Ahead of Print: May 26, 2011 Accepted: March 22, 2011 Submitted: October 7, 2010 grouped by contraction type, sex, joint or muscle group, intensity, or activity level; and (3) further subgrouped between contraction type and the remaining moderators. Out of 3,457 potential studies, 46 publications (with 78 distinct effect size data points) met all inclusion criteria. Limitations. A lack of available data limited subgroup analyses (ie, sex, intensity, joint), as did a disproportionate spread of data (most intensities ⱖ50% of maximum voluntary contraction). Conclusions. Overall, older adults were able to sustain relative-intensity tasks significantly longer or with less force decay than younger adults (effect size⫽0.49). However, this age-related difference was present only for sustained and intermittent isometric contractions, whereas this age-related advantage was lost for dynamic tasks. When controlling for contraction type, the additional modifiers played minor roles. Identifying muscle endurance capabilities in the older adult may provide an avenue to improve functional capabilities, despite a clearly established decrement in peak torque. August 2011 Volume 91 Number 8 Post a Rapid Response to this article at: ptjournal.apta.org Physical Therapy f 1153 Age-Related Muscle Fatigue: A Meta-analysis A lthough it is well recognized that sarcopenic changes in aging adults result in diminished muscle mass and subsequent loss of strength (force-generating capacity),1,2 it is less clear how aging affects the properties of muscle fatigue. A greater understanding of muscle fatigue capabilities across the life span may influence clinical decision making and affect therapeutic exercise prescription. Although older adults may be commonly perceived as fatiguing more readily, resistance to muscle fatigue actually may improve with age.3 Perceptions of fatigue may be reported as a “feeling of tiredness” or “lack of energy,”4 which can be distinct from muscle fatigue, defined as, “any exercise-induced reduction in the ability to exert muscle force or power, regardless of whether or not the task can be sustained.”5(p691) Several studies have been performed to assess differences in resistance to muscle fatigue in young adults versus old adults. However, to date, these data have not been systematically compiled to determine whether older adults indeed have consistently greater muscle endurance than young adults and which factors may influence these age-related differences. Muscle fatigue can vary greatly within and between individuals due to the complex nature of fatigue. That is, muscle fatigue capabilities can vary between contraction types (isometric versus isokinetic),6 joints or muscle groups,7 task intensities,8 and position-matching versus forcematching paradigms.9 In addition, Available With This Article at ptjournal.apta.org • Discussion Podcast with authors Keith Avin and Laura Frey Law. Moderated by Carolynn Patten. 1154 f Physical Therapy Volume 91 muscle fatigue may differ between men and women10,11 or with physical activity status.12 These factors may have the potential to influence age-related muscle fatigue properties. To date, only small-scale reviews have provided insights into subsets of the research available to ascertain age-related differences in muscle fatigue properties.3,13 Despite the number of available studies on muscle fatigue, our understanding of age-related changes in fatigue remains incomplete. Properly indentifying capabilities in older adults may affect dose-response relationships and modify therapeutic exercise interventions. Thus, the purpose of this study was to characterize differences in muscle fatigue between young and old adults using systematic meta-analysis techniques to compile the available literature. Effect sizes were used to assess the degree to which young or old adults were more fatigable considering all data, as well as preplanned subgroupings based on contraction type, sex, joint region, task intensity, and physical activity levels, when possible. Method Database Review A 2-stage systematic review of the literature was used to identify studies on muscle fatigue including both old and young adults. Stage 1 involved searches of the following databases: PubMed (1948 to June 28, 2010), the Cumulative Index to Nursing and Allied Health Literature (CINAHL; 1937 to June 28, 2010), PEDro (1929 to June 28, 2010), EBSCOhost: ERIC (1966 to June 28, 2010), EBSCOhost: Sportsdiscus (1888 to June 28, 2010), and The Cochrane Library (1993 to June 28, 2010). A total of 11 search terms and key word combinations were used to elicit relevant articles, including: “endurance,” “fatigue,” “aging adult,” “older adult,” “intermittent fatigue,” Number 8 “isokinetic fatigue,” and “isometric fatigue.” For example, a search performed in PubMed (accessed October 5, 2009) using the key words “aging” and “fatigue” yielded 600 related articles. The inclusion and exclusion criteria (see below) were used to include studies providing young versus old adult muscle fatigue data. Stage 2 involved reviewing bibliographies of studies meeting the inclusion criteria of stage 1 to find additional relevant fatigue studies. All abstracts were first screened for studies that reported the performance of a relative-intensity fatigue task, including young and old adult cohorts. These studies then were retrieved in full text and reviewed by both authors to ensure agreement on inclusion and exclusion criteria, and all entered data were reviewed twice against the original articles to decrease the likelihood of transcription errors. Inclusion and Exclusion Criteria The following criteria were used for study inclusion: human participants who were healthy; young cohort mean age between 18 and 45 years and older cohort mean age ⱖ55 years; sustained isometric, intermittent isometric, isokinetic, or isotonic tasks using relative intensities based on maximum voluntary contraction (% MVC); outcome measures of either time to task failure (ie, endurance time) or reduction in peak torque (ie, fatigue index); single-joint involvement (per fatigue task); and publication in English. Studies were excluded if they used electrical stimulation to elicit fatigue, simultaneous multijoint testing, or functional tasks that did not assess torque as a percentage of the maximum value or that used body or limb weight as the primary resistance (eg, Sorensen test). In addition, if variance information (eg, standard deviation) was not reported or was unattainable from the authors, studies were excluded. Inclusion and exclusion criteria did August 2011 Age-Related Muscle Fatigue: A Meta-analysis not account for athletic training status or level of physical activity, but when reported, this information was utilized. Quality assessment of included studies did not require the traditional approaches used for meta-analyses to assess interventions, such as blinded investigators, placebo-controls, or random assignment. Rather, the powerful statistical application of meta-analysis was used with observational studies to systematically compile the data available to better distinguish fatigue capabilities in the older versus younger adults, considering several possible moderating variables. Outcome Variables To characterize differences in muscle fatigue between 2 groups, protocols typically utilize relative-intensity tasks (% MVC) to standardize task demands between individuals. Muscle fatigue properties are assessed indirectly, either by the duration a relative-intensity task can be sustained (ie, endurance time) or the percentage of baseline peak force remaining following the performance of a task for a preset duration. Most studies reported only 1 of these 2 outcome variables, but occasionally those involving intermittent tasks reported both. When this occurred, only the percentage of change in peak force was used in the meta-analysis, as this was the preferred outcome variable reported for intermittent tasks. Greater muscle fatigue is observed as shorter endurance times or lower percentages of baseline torque values. Endurance time usually is reported as the total duration a relativeintensity task can be maintained until the target muscle torque falls to 5% to 10% below target levels. Only acute muscle fatigue was assessed in this study (ie, immediate or short-term outcomes, rather than long-duration decrements in forceAugust 2011 producing capability associated with low-frequency fatigue). Relevant endurance or fatigue data reported only in graphic form were extracted using pixel analysis (Adobe Photoshop*) to determine the respective numerical values. Means and standard deviations for young and old cohorts were recorded for each pair of data. Moderating Variables Additional study information was recorded for analysis, including sample size, sex, mean age for each cohort (young, old), standardized task intensity (from 1% to 100% of maximum), contraction type (sustained isometric, intermittent isometric, and isokinetic), joint region tested (eg, ankle, back, elbow), joint angle, torque direction (eg, flexion, extension), and physical activity level (when reported). When outcome measures were not reported separately by sex and were unavailable following attempts to contact the corresponding authors, the data were coded simply as “mixed sex.” Contractions were classified as 1 of 3 types: 2 static (isometric with [sustained] or without [intermittent] rest intervals) and 1 dynamic (isokinetic). Task intensity was categorized as low (ⱕ33% of maximum), moderate (34%– 66% of maximum), or high (ⱖ67% of maximum), regardless of contraction type. Given the varying methods for quantifying physical activity, data were dichotomized to active or inactive when available. When necessary, the data for multiple age cohorts (eg, for 20 –29 and 30 –39 years) were combined using weighted means and pooled standard deviations.14 When multiple task intensities (eg, 30% and 50% of maximum) or joint regions (eg, ankle and elbow) were reported in a single manuscript, data for each fatigue * Adobe Systems Inc, 345 Park Ave, San Jose, CA 95110. task were included (in separate rows) rather than combining them into a single mean or selecting only one task per study. We chose this strategy to minimize any potential self-selection bias or missing potential effects due to joint or intensity factors. Although this approach allows for multiple measures that are not fully independent, particularly for observational studies, it is challenging to determine whether independence is ensured across publications (by the same authors). That is, the same patient population may be recruited for studies reported in multiple publications. Statistical Analyses Effect size is the standardized mean difference between 2 populations (ie, young versus old). Hedges’ g was chosen as the best effect size estimate due to its correction for slight overestimations that may occur with small samples.15 Mean effect sizes (and associated variances) across studies were calculated (Comprehensive Meta-Analysis†) using a mixed-effects model determined a priori (random and fixed effects). A random-model approach was chosen under the guise of generalizing results among the older population and inherent inequality of effect sizes across studies. A fixed subgroup analysis assumes results will generalize to the specific variables of interest such as contraction type (eg, sustained isometric, intermittent isometric, isokinetic), intensity, and so on. Results are presented such that positive effect size values indicate older adults are more resistant to fatigue, whereas negative effect size values indicate young adults are more resistant to fatigue. Analyses were stratified into 3 levels (Fig. 1), with preplanned subgrouping categories. A specific subgroup was included in comparisons only if † Volume 91 Biostat, 14 N Dean St, Englewood, NJ 07631. Number 8 Physical Therapy f 1155 Age-Related Muscle Fatigue: A Meta-analysis Stage 1: 3,445 related records identified through database searches Stage 2: 48 records identified through citation search of included articles 3,457 records after duplicates removed 3,457 records screened 3,372 records excluded 39 records excluded: • 1–Nonvoluntary • 1–No variance data • 1–Outcome variables • 2–Multiple joints • 12–Old adults only • 12–Young adults only • 2–Patient cohort only • 7–Limited time duration or no fatigue • 1–No age specified 85 full-text articles assessed for eligibility 46 studies included in quantitative synthesis (meta-analysis) (78 data points) Figure 1. Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow diagram of the literature search. ogeneity among the data included, whereas the I2 index is better able to quantify the magnitude of the heterogeneity.16 We operationally defined the magnitude of heterogeneity as low (I2ⱕ33%), moderate (34%ⱕI2⬍67%), and high (I2ⱖ67%), based on previous suggestions.17 Heterogeneity estimates were evaluated at each level of analysis. Results are reported as mean summary effect sizes (with P values) for each subgroup analysis. A more stringent alpha level than conventionally used (␣ⱕ.01) was chosen to minimize both type I and II errors.18 Observational studies are less likely than interventional studies to be adversely affected by publication bias, as identifying a fatigue advantage in either direction would be deemed a valuable scientific contribution. Furthermore, several studies investigated other aspects of muscle fatigue, such that the data relevant to this meta-analysis were not necessarily the primary outcomes (accordingly, lack of age-related fatigue differences would not influence likelihood of publication). Therefore, our analyses were not further extended for publication bias within or between studies. Results it included data from a minimum of 3, separate published studies; thus, the final set of subgroups was determined by the data available. The level I analysis determined a single composite effect size for resistance to fatigue for old versus young groups, including all data points with no subgroups. Level II analyses included subgrouping by single individual categories (sex, contraction type, intensity, joint tested, and activity level) to the extent sufficient data were available. Level III analyses involved further subgrouping the contraction types from level II, such as comparing intensity levels, sex, 1156 f Physical Therapy Volume 91 or joints within each contraction type (eg, interaction or moderated effects), when sufficient data were available. Level III subgroupings were considered only when sufficient data were available (ie, 3 or more independent studies). The goal of a meta-analysis is to not only compute summary effect sizes but also determine the extent of variation present in the true effect size (ie, heterogeneity), suggesting whether additional moderating variables are involved. Heterogeneity was quantified via the I2 index and the Q test.15 A significant Q statistic indicates only the presence of heter- Number 8 Database Review Initial search strategies (stages 1 and 2) resulted in 3,457 potential studies (after duplicates were removed), with 46 studies meeting all inclusion criteria (Fig. 1). Several studies reported on more than one joint or muscle group, contraction type, or task intensity, for a total of 78 young adult versus old adult fatigue comparisons (ie, individual effect sizes) to analyze. The numbers of data points per subgroup comparison are detailed in the Table. Level I: Overall Age Effect The level I analysis, using all 78 individual effect sizes, revealed that August 2011 Age-Related Muscle Fatigue: A Meta-analysis Table. Summary of Heterogeneity Statistics for Each Subgroup Analysis Analysis Level na Q Test (P Value)b I2 Index (%) 78 ⬍.001 56.4 Sustained isometric 45 .005 38.9 Intermittent isometric 16 .652 0.0 Subgrouping Intensity Level I Level II, contraction Isokinetic 16 .001 60.4 Level II, sex Male 45 ⬍.001 58.9 Female 18 .006 51.8 Level II, intensity Low 15 ⬍.001 73.8 Level II, joint Level II, activity Level III, contraction/intensity Level III, contraction/sex Level III, contraction/joint Level III, contraction/activity Moderate 25 .081 29.8 High 38 ⬍.001 57.1 Ankle 17 .018 68.7 Elbow 14 .024 47.7 Hand 16 .183 23.9 Knee 22 ⬍.001 57.5 Active 44 ⬍.001 55.1 Inactive 11 .512 0.0 Low 14 .004 57.4 Moderate 21 .036 38.8 High 10 .692 0.0 3 .554 0.0 Sustained isometric Intermittent isometric Moderate High 13 .582 0.0 Sustained isometric Male 29 .006 44.6 Female 8 .236 24.2 Intermittent isometric Male 8 .449 0.0 Female 4 .709 0.0 Isokinetic Male 7 .001 74.3 Female 6 .336 12.4 Sustained isometric Ankle 4 .015 71.5 Elbow 12 .030 48.4 Hand 13 .669 0.0 Knee 7 .237 25.2 Intermittent isometric Ankle 9 .960 0.0 Isokinetic Ankle 3 .002 83.5 Knee 13 .031 46.9 Active Sustained isometric Intermittent isometric Isokinetic 30 .064 29.8 Inactive 4 .739 0.0 Active 7 .289 18.5 Inactive 6 .750 0.0 Active 8 .004 66.4 a Number of data points per analysis level. b P values are uncorrected for multiple comparisons. August 2011 Volume 91 Number 8 Physical Therapy f 1157 Age-Related Muscle Fatigue: A Meta-analysis Article % Maximum Hedges’ g SE P Hand M NA 50 0.36 0.35 .309 Bazzucchi et al, 20058 Elbow M Active 30 0.27 0.54 .620 Bazzucchi et al, 20058 Elbow M Active 50 1.72 0.64 .007 20058 Elbow M Active 80 1.26 0.59 .033 Bilodeau et al, 200120 Elbow MX Inactive 100 0.70 0.43 .104 200120 Bilodeau et al, Sex Activity Level Aniansson et al, 197819 Bazzucchi et al, Joint Elbow MX NA 35 1.53 0.50 .002 Chatterjee and Chowdhuri, 199122 Hand M Inactive 40 0.12 0.34 .719 Christie and Kamen, 200923 Ankle MX Active 50 ⫺0.68 0.49 .163 Griffith et al, 201024 Ankle MX Active 30 0.64 0.38 .091 Hara et al, 199825 Hand MX Inactive 50 0.56 0.49 .253 Huang et al, 200726 Hand MX NA 75 0.89 0.39 .021 200410 Elbow M NA 20 1.98 0.49 .000 Hunter et al, 200410 Elbow F NA 20 0.32 0.43 .465 200527 Hunter et al, Elbow M NA 20 1.42 0.54 .008 Johnson, 198228 Knee F Active 50 0.32 0.36 .365 Lanza et al, 200529 Ankle M Inactive 100 0.33 0.48 .492 Larsson and Karlsson, 19781 Knee M Active 50 0.42 0.36 .244 Mademli and Arampatzis, 200830 Ankle M Active 40 1.40 0.43 .001 Mademli et al, 200831 Knee M Active 25 1.15 0.41 .005 Hand MX NA 40 0.56 0.49 .254 Hand M NA 40 0.03 0.27 .907 Hunter et al, Momen et al, 200432 Petrofsky et al, 197533 Petrofsky and Lind, 197534 Hand F NA 40 0.72 0.28 .010 Petrofsky and Laymon, 200235 Hand M NA 40 1.15 0.40 .004 200235 Petrofsky and Laymon, Knee M NA 40 1.43 0.41 .001 Petrofsky et al, 200936 Hand MX Active 40 0.45 0.36 .207 Smolander et al, 199837 Hand M Active 20 0.18 0.47 .695 Smolander et al, 199837 Hand M Active 40 0.46 0.47 .333 199837 Hand M Active 60 0.29 0.47 .542 Smolander et al, 199837 Knee M Active 20 0.30 0.47 .530 199837 Knee M Active 40 0.19 0.47 .682 Smolander et al, 199837 Knee M Active 60 0.39 0.47 .408 Smolander et al, Smolander et al, Taylor et al, 199138 Hand M Active 30 0.28 0.37 .455 Yassierli et al, 200739 Shoulder M Active 30 0.60 0.29 .039 Yassierli et al, 200739 Shoulder M Active 50 0.40 0.29 .165 Yassierli et al, 200739 Shoulder M Active 70 0.21 0.28 .465 200739 Back M Active 30 0.44 0.40 .272 Yassierli et al, 200739 Back M Active 50 0.28 0.40 .475 200739 Back M Active 70 0.12 0.39 .767 Yassierli et al, 200739 Back F Active 30 ⫺0.12 0.39 .753 Yassierli et al, Yassierli et al, (Continued) Figure 2. Forest plot of individual effect sizes for sustained isometric contractions only, with their corresponding subgrouping categories for sex, joint, task intensity, and physical activity level. Positive effect sizes indicate greater fatigue resistance for older adults, whereas negative effect sizes indicate greater fatigue resistance for younger adults. SE⫽standard error, CI⫽confidence interval, M⫽male, F⫽female, MX⫽mixed, NA⫽not available. 1158 f Physical Therapy Volume 91 Number 8 August 2011 Age-Related Muscle Fatigue: A Meta-analysis Article % Maximum Hedges’ g SE P Back F Active 50 0.15 0.39 .696 Yassierli et al, 200739 Back F Active 70 0.00 0.39 1.000 Yoon et al, 200840 Elbow M Active 20 3.17 0.84 .000 200840 Elbow M Active 80 0.64 0.55 .247 Yoon et al, 200840 Elbow F Active 20 1.52 0.51 .003 Elbow F Active 80 Yoon et al, 200840 Isometric Summary Sex Activity Level Yassierli et al, 200739 Yoon et al, Joint (Fixed) 0.44 0.45 .332 0.53 0.06 .000 Figure 2. Continued older adults were significantly more resistant to acute muscle fatigue (greater muscle endurance) than young adults, with a moderate mean effect size of 0.49 (95% confidence interval⫽0.35– 0.63). Forest plots showing individual effect sizes by Article Joint contraction type are presented in Figures 2, 3, and 4. Figure 5 illustrates the effect sizes for each analysis level. One isotonic effect size was included in the overall analysis, but was not extended to a separate Sex Activity Level contraction-type subgroup due to a lack of comparative studies. Level II Subgroups Contraction type. Older adults demonstrated greater muscle fatigue resistance (ie, more endurant) for % Maximum Hedges’ g SE P 60 0.24 0.54 .656 Allman and Rice, 200341 Elbow M Active Allman and Rice, 200142 Elbow M Active 60 0.42 0.51 .409 Callahan et al, 200943 Knee MX Inactive 100 1.16 0.38 .002 Hand MX Active 100 1.36 0.49 .006 Ankle M NA 100 0.97 0.42 .020 200046 Hand M Active 100 1.85 0.52 .000 Ditor and Hicks, 200046 Hand F Active 100 0.77 0.45 .085 200247 Ankle M Inactive 100 0.74 0.43 .082 Kent-Braun et al, 200247 Ankle F Inactive 100 1.20 0.47 .010 Lanza et al, 200448 Ankle M Active 100 0.54 0.46 .242 Lanza et al, 200749 Ankle MX Inactive 100 0.90 0.33 .007 Chan et al, 200044 Chung et al, 200745 Ditor and Hicks, Kent-Braun et al, Mademli and Arampatzis, 200850 Ankle M NA Rubinstein and Kamen, 200551 Ankle F Active 65 0.94 0.44 .033 100 0.86 0.34 .012 Russ et al, 200852 Ankle M Inactive 100 0.48 0.49 .335 Russ et al, 200852 Ankle F Inactive 100 0.43 0.47 .361 Stackhouse et al, 200153 Knee MX NA 100 Intermittent Isometric Summary (Fixed) 0.34 0.34 .318 0.82 0.11 .000 Figure 3. Forest plot of individual effect sizes for intermittent isometric contractions only, with their corresponding subgrouping categories for sex, joint, task intensity, and physical activity level. Positive effect sizes indicate greater fatigue resistance for older adults, whereas negative effect sizes indicate greater fatigue resistance for younger adults. SE⫽standard error, CI⫽confidence interval, M⫽male, F⫽female, MX⫽mixed, NA⫽not available. August 2011 Volume 91 Number 8 Physical Therapy f 1159 Age-Related Muscle Fatigue: A Meta-analysis Article Joint Sex Activity Level M NA Aniansson et al, 197819 Knee Aniansson et al, 197819 Knee F Baudry et al, 200754 Ankle F Callahan et al, 200943 % Maximum Hedges’ g SE P 100 0.25 0.35 .476 NA 100 ⫺0.03 0.33 .917 NA 100 ⫺0.46 0.35 .188 Knee MX Inactive 100 0.09 0.36 .816 Johnson, 198228 Knee F Active 100 ⫺0.31 0.36 .387 Laforest et al, 199012 Knee MX MX 100 ⫺0.09 0.22 .686 Lanza et al, 200448 Ankle M Active 100 1.72 0.55 .002 Larsson and Karlsson, 19781 Knee M Active 100 0.20 0.43 .644 Lindstrom et al, 199755 Knee M Active 100 ⫺0.47 0.43 .280 Lindstrom et al, 199755 Knee F Active 100 0.74 0.49 .134 Lindstrom et al, 200656 Knee F Active 100 0.12 0.47 .809 200656 Knee M Active 100 ⫺1.13 0.46 .014 Knee M Active 50 0.31 0.38 .421 Ankle MX NA 100 0.55 0.28 .046 Knee M NA 100 0.98 0.35 .005 Knee F NA 100 ⫺0.40 0.23 .085 0.05 0.09 .564 Lindstrom et al, Mademli et al, 200831 Muller et al, 200758 Rawson, 200959 Schwendner et al, 199760 Isokinetic Summary (Fixed) Figure 4. Forest plot of individual effect sizes for isokinetic contractions only, with their corresponding subgrouping categories for sex, joint, task intensity, and physical activity level. Positive effect sizes indicate greater fatigue resistance for older adults, whereas negative effect sizes indicate greater fatigue resistance for younger adults. SE⫽standard error, CI⫽confidence interval, M⫽male, F⫽female, MX⫽mixed, NA⫽not available. both sustained (Fig. 2) and intermittent (Fig. 3) isometric contractions, but the intermittent tasks showed the greatest age-related advantage compared with sustained tasks (effect size⫽0.82 versus 0.52, P⫽.009; Fig. 5). However, for dynamic contractions, no age-related difference in muscle fatigue was observed (effect size⫽0.05, Fig. 4). Sex. Older adults of both sexes were more fatigue resistant than younger adults. This age-related advantage, however, was greater for men than for women (P⫽.009) when not accounting for any additional moderating factors (Fig. 5). Joint. Older adults were significantly more fatigue resistant than young adults across all joint region subgroups assessed (ie, ankle, 1160 f Physical Therapy Volume 91 elbow, hand, and knee joint regions had sufficient data available). However, these effect sizes differed among joints (P⬍.008), with the exception of the ankle versus the hand joint regions (P⫽.42). The largest effect size was observed at the elbow and the smallest effect size was observed at the knee, when not accounting for any additional factors (Fig. 5). However, the elbow joint tasks comprised solely static contraction protocols, whereas the knee included both isometric and isokinetic testing (see level III subgrouping below). Intensity. Older adults were more resistant to fatigue across all intensity levels (low, moderate, and high) (Fig. 5). Although effect sizes decreased with increasing intensity (ie, the fatigue advantage with Number 8 advancing age decreased at higher intensities), none of the differences achieved significance (P⬎.067) (Fig. 5). Physical activity. Older adults were more resistant to fatigue across active and inactive cohorts, with the difference in effect sizes between subgroups just beyond significance (P⫽.063). Level III Analyses Contraction type ⴛ intensity. Although task intensity moderated the age-related fatigue advantage overall (see level II above), this effect was lost or reversed when controlling for contraction type (Fig. 5). For sustained isometric contractions, older adults remained more fatigue resistant than young adults across all intensities (low, moderate, and August 2011 Age-Related Muscle Fatigue: A Meta-analysis Level Hedges’ g Subgroupings SE P 0.49 0.07 ⬍.001 Sustained isometric 0.53 0.06 ⬍.001 Intermittent isometric 0.82 0.10 ⬍.001 Level I, all Level II, contraction type Isokinetic 0.05 0.08 .358 Level II, sex Male 0.49 0.06 ⬍.001 Female 0.23 0.09 .005 Level II, intensity Low 0.51 0.11 ⬍.001 Level II, joint Level II, activity Level III, contraction/ intensity Level III, contraction/sex Moderate 0.50 0.08 ⬍.001 High 0.35 0.06 ⬍.001 Ankle 0.51 0.10 ⬍.001 Elbow 0.97 0.14 ⬍.001 Hand 0.55 0.09 ⬍.001 Knee 0.20 0.08 .003 Active 0.39 0.06 ⬍.001 Inactive 0.60 0.12 ⬍.001 Sustained isometric Low 0.67 0.11 ⬍.001 Moderate 0.50 0.08 ⬍.001 High 0.41 0.13 .005 Intermittent isometric Moderate 0.58 0.28 .128 High 0.85 0.11 ⬍.001 Sustained isometric Male 0.55 0.08 ⬍.001 Female 0.40 0.14 .003 Intermittent isometric Male 0.78 0.17 ⬍.001 Female 0.82 0.21 ⬍.001 Isokinetic Male 0.26 0.15 .054 ⫺0.20 0.14 .268 Sustained isometric Ankle 0.51 0.22 .020 Elbow 1.08 0.15 ⬍.001 Hand 0.44 0.10 ⬍.001 Female Level III, contraction/ joint Level III, contraction/ activity Knee 0.61 0.16 ⬍.001 Intermittent isometric Ankle 0.81 0.14 ⬍.001 Isokinetic Ankle 0.37 0.20 .106 Knee ⫺0.02 0.09 .807 Active 0.44 0.08 ⬍.001 Inactive 0.38 0.21 .07 Active 0.86 0.18 ⬍.001 Inactive 0.85 0.17 ⬍.001 Active 0.05 0.15 .344 Sustained isometric Intermittent isometric Isokinetic Figure 5. Forest plot of summary effect sizes for each subgrouping category (level I–III). Positive effect sizes indicate greater fatigue resistance for older adults, whereas negative effect sizes indicate greater fatigue resistance for younger adults. SE⫽standard error, CI⫽confidence interval. August 2011 Volume 91 Number 8 Physical Therapy f 1161 Age-Related Muscle Fatigue: A Meta-analysis high), with no significant difference exhibited among intensity subgroups (Pⱖ.07). Conversely, for intermittent isometric contractions, no significant age differences occurred for moderate intensities, whereas a large effect size was observed for high intensities (insufficient low-intensity, intermittent task data available). Although these findings demonstrate opposing influences of intensity on intermittent tasks than observed with the sustained isometric tasks (or overall in level II), only 3 of the 16 intermittent tasks were performed at a moderate intensity. Contraction type ⴛ sex. Although sex was a significant moderator of the age-related endurance advantage in the level II analyses, it was not a significant moderator when considering each contraction type separately. Older adults (both men and women) remained more fatigue resistant for sustained and intermittent isometric tasks, but did not differ between sexes (P⬎.17) (Fig. 5). Furthermore, no age-related advantage was observed in either men or women (effect sizes not significantly different than zero) for the isokinetic contractions. Contraction type ⴛ joint. Similarly, further subgrouping contraction type by joint region slightly altered the findings from the previous level II analyses. Within sustained isometric contractions, older adults were more fatigue resistant across the joints considered (elbow, hand, and knee joint regions, with the ankle just surpassing our stringent critical value). However, only the elbow continued to result in significantly larger effect sizes than the remaining joints, with the knee now exhibiting effect sizes similar to those of the hand and ankle (Fig. 5). For intermittent isometric contractions, the ankle (only subgroup possible) demonstrated significant age1162 f Physical Therapy Volume 91 related advantages in muscle fatigue. During isokinetic contractions, neither the ankle nor the knee (the only joints with sufficient data) demonstrated any age-related advantage (or disadvantage) in fatigue resistance (Pⱖ.06). Overall, joint region had only mild moderating influences on the fatigue differences observed between young versus old adults when controlling for contraction type. Contraction type ⴛ physical activity. Physical activity did not substantially alter the previous contraction-type subgroups (Fig. 5). Older adults were significantly more fatigue resistant across each combination of sustained and intermittent isometric contraction types and activity levels except for the inactive, sustained isometric group, which likely was underpowered (n⫽4, effect size⫽0.38, P⫽.07). The age-related fatigue advantage did not differ significantly between the active and inactive groups for isometric or intermittent tasks (P⬎.40). Heterogeneity Overall, heterogeneity was categorized as low to moderate for all levels of the meta-analysis (Tab. 1). The proportion of subgroups categorized with low heterogeneity increased from 28.6% for level II analyses to 60.9% for level III analyses. The increased proportion of low heterogeneity with additional subgroup analyses suggests that several moderators identified in this analysis (eg, contraction type, joint, intensity) contributed to variations in agerelated fatigue resistance. Although the level III heterogeneity increased at the ankle for both sustained and isokinetic contractions, the limited number of data points (4 and 3, respectively) demonstrated the difficulty in attaining a consistent summary effect size. Additional data are needed to fully characterize agerelated fatigue differences. Number 8 Discussion This is the first study to systematically compile outcomes data to characterize age-related differences in muscle fatigue considering several potential moderating variables: contraction type, intensity, sex, joint region, and activity level. The primary finding of this meta-analysis is that muscle fatigue resistance is enhanced with age for relativeintensity tasks when additional intrinsic and extrinsic factors are not considered (level I analysis). This age-related advantage in fatigue resistance occurred for both sustained and intermittent isometric contractions, but is lost for isokinetic contractions. Improved fatigue resistance with advancing age is consistent with several reported changes in muscle properties with aging. A preferential atrophy of type II fibers1,61 and preferential loss of fast motor units2 have been observed with advancing age and sarcopenia. These changes would result in a greater proportion of type I or slow, oxidative fibers, which may account for greater fatigue resistance during relativeintensity tasks (ie, tasks standardized to maximum strength). However, this adaptation did not prove beneficial under all conditions (ie, dynamic tasks). Level II and III analyses revealed older adults were more endurant than young adults for sustained and intermittent isometric (static) contractions, but not for isokinetic (dynamic) contractions. This result is somewhat surprising, as we anticipated the intermittent isometric contractions to behave similarly to isokinetic contractions, as greater muscle reperfusion, replenishment of oxygenated blood, and removal of metabolic wastes might be facilitated under both conditions. To the contrary, the intermittent tasks resulted in the greatest age-related fatigue August 2011 Age-Related Muscle Fatigue: A Meta-analysis advantage, whereas isokinetic tasks showed no age-related differences. Thus, the inclusion of rest intervals, and accordingly muscle reperfusion, does not appear to be the key variable, but rather the contraction type itself appears to be of importance in age-related endurance changes. One explanation may be that the proportional shift toward type I fibers and the slowing of both contraction and relaxation times that occurs with aging may cause a leftward shift in the force-frequency curve62 and a leftward and downward shift in the force-velocity curve.63 Thus, although the muscle fibers are slower and rely on greater oxidative energy sources, they may be less able to maintain power (ie, force ⫻ velocity) over time. These adaptations may enable the older adult to be more fatigue resistant for isometric contractions (slower, oxidative fibers), but not during dynamic contractions, where impaired power generation would be expected to have its greatest impact. Anecdotal perceptions of muscle fatigue increasing with advancing age are in opposition to the controlled research findings of greater fatigue resistance with aging. This finding may be partially explained by the differences observed between static and dynamic tasks, as many functional tasks (eg, sit-to-stand maneuver, ambulation) require dynamic rather than static contractions. However, even with dynamic tasks, older adults are not disadvantaged; thus, this potential discrepancy may be further attributed to differences between absolute- and relative-intensity conditions. Functional tasks (eg, stair climbing) require absolute loads that are not proportional to peak strength. As the older adult weakens with age,1,2 functional tasks can require a greater percentage of maximal capacity; thus, tasks are performed at a higher August 2011 relative intensity.64 Fatigue occurs more rapidly with increasing task intensity; maximum endurance time decreases nonlinearly with increasing task intensity.7 Thus, although resistance to fatigue may improve with age for a relative-intensity (eg, 50% of maximum) task that is standardized among individuals, the increased relative workload for a functional task may offset any age advantage. That is, if a given task requires 40% of maximum strength for a young adult, but 60% for an older adult, the apparent task endurance may be less for the older adult, even if underlying muscle fatigue resistance is greater with age. Interpretation of the remaining potential moderators (sex, physical activity, intensity, and joint) associated with age-related differences in muscle fatigue is somewhat challenging given the incomplete data available for each possible subgrouping. No significant differences between men and women were consistently observed in this meta-analysis, once contraction type was controlled for, which is in agreement with conclusions drawn from several individual studies19,46,47 but in opposition to others.10 Current comparisons did not assess whether sex differences in muscle fatigue occurred, but rather whether age differences varied by sex. Lastly, greater physical activity did not influence the age-related fatigue advantage. However, these findings are based on smaller subgroup samples, with heterogeneous definitions of active versus inactive individuals, and thus may reflect less stability in effect size estimates. Although the current meta-analysis was able to identify differences in muscle fatigue properties across contraction types between young and old adults, there are several limitations that should be acknowledged. Several subgrouping comparisons in levels II and III for joint, intensity, and contraction type were not performed due to a lack of available data. The majority of intermittent isometric and isokinetic protocols were performed at intensities of 50% MVC or higher (most at 100%), limiting the interpretation intensity has upon fatigue differences with aging for these contraction types. Intermittent tasks were further limited by the disproportionate number of comparisons including men (8 men versus 4 women) and limited joint regions that have been tested (ankle⫽9, all others combined⫽7). Physical activity data were classified simply as active versus sedentary, which may miss subtle influences of varying levels of physical activity. Lastly, we included studies with cohorts aged ⱖ55 years, thus a relatively “young” older adult minimum age criterion. Secondary analyses demonstrated no significant difference in effect size estimates if we had used only studies with adults over 60 years as our age minimum criterion. These findings suggest the need for future studies to explicitly report fatigue data by sex and provide physical activity information for both young and old adult cohorts when possible. Additional fatigue studies involving isokinetic and intermittent tasks using the upper extremities and lower intensities would help to minimize the potential bias and interactions present among muscle group, intensity, and contraction type, as observed here. In particular, it is not clear why this age-related advantage is lost during dynamic contractions, which would benefit from research considering potential influences such as: task complexity, passive tissue contributions, and muscle power. Finally, although these findings provide greater insight into age-related changes in muscle fatigue properties, additional research is needed to clarify the magnitude and impact of this potential Volume 91 Number 8 Physical Therapy f 1163 Age-Related Muscle Fatigue: A Meta-analysis benefit and whether it can be further altered by therapeutic interventions. Despite the abundance of acute muscle fatigue research, few studies have attempted to compile all of the available data on age-related differences in fatigue resistance. This meta-analysis supports that aging results in a general muscle fatigue resistance advantage, but this advantage is particularly dependent on contraction type. Dynamic tasks, specifically isokinetic tasks, were not found to exhibit any advantage (or disadvantage) in muscle fatigue for old versus young adults. The underlying mechanisms for these findings remain somewhat unclear, but may be due to a greater loss of muscle power with aging. Ultimately, these age-related fatigue differences may help offset the deleterious effects of sarcopenia and loss of muscle strength. In light of a reduction in strength, therapeutic interventions may target muscle fatigue resistance to affect functional capabilities in the older adult. Both authors provided concept/idea/project design, writing, data collection and analysis, and project management. A poster presentation of this research was given at the Combined Sections Meeting of the American Physical Therapy Association; February 17–20, 2010; San Diego, California. The authors were funded, in part, by National Institute of Arthritis and Musculoskeletal and Skin Diseases/National Institutes of Health grant K01AR056134, National Research Service Award 1 F31 AR056175, and the Foundation for Physical Therapy. DOI: 10.2522/ptj.20100333 References 1 Larsson L, Karlsson J. Isometric and dynamic endurance as a function of age and skeletal-muscle characteristics. Acta Physiol Scand. 1978;104:129 –136. 2 Lexell J. Human aging, muscle mass, and fiber type composition. J Gerontol A Biol Sci Med Sci. 1995;50 Spec. No.:11–16. 1164 f Physical Therapy Volume 91 3 Kent-Braun JA. Skeletal muscle fatigue in old age: whose advantage? Exerc Sport Sci Rev. 2009;37:3–9. 4 St Clair Gibson A, Baden DA, Lambert MI, et al. The conscious perception of the sensation of fatigue. Sports Med. 2003;33: 167–176. 5 Bigland-Ritchie B, Woods JJ. Changes in muscle contractile properties and neural control during human muscular fatigue. Muscle Nerve. 1984;7:691– 699. 6 Hunter SK. Aging and Mechanisms of Task-dependent Muscle Fatigue. Kerala, India: Research Signpost; 2009. 7 Frey Law LA, Avin KG. Endurance time is joint-specific: a modelling and metaanalysis investigation. Ergonomics. 2010; 53:109 –129. 8 Bazzucchi I, Marchetti M, Rosponi A, et al. Differences in the force/endurance relationship between young and older men. Eur J Appl Physiol. 2005;93:390 –397. 9 Hunter SK, Rochette L, Critchlow A, Enoka RM. Time to task failure differs with load type when old adults perform a submaximal fatiguing contraction. Muscle Nerve. 2005;31:730 –740. 10 Hunter SK, Critchlow A, Enoka RM. Influence of aging on sex differences in muscle fatigability. J Appl Physiol. 2004;97:1723– 1732. 11 Avin KG, Naughton MR, Ford BW, et al. Sex differences in fatigue resistance are muscle group dependent. Med Sci Sports Exerc. 2010;42:1943–1950. 12 Laforest S, St-Pierre DM, Cyr J, Gayton D. Effects of age and regular exercise on muscle strength and endurance. Eur J Appl Physiol Occup Physiol. 1990;60:104 –111. 13 Allman BL, Rice CL. Neuromuscular fatigue and aging: central and peripheral factors. Muscle Nerve. 2002;25:785–796. 14 Higgins J, Green S, eds. Cochrane Handbook for Systematic Reviews of Interventions. Version 5.02. Available at: http:// www.cochrane-handbook.org. Accessed April 5, 2010. 15 Borenstein M. Introduction to Meta-analysis. Chichester, West Sussex, United Kingdom: John Wiley & Sons Ltd; 2009. 16 Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002;21:1539 –1558. 17 Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in metaanalyses. BMJ. 2003;327:557–560. 18 Garamszegi LZ. Comparing effect sizes across variables: generalization without the need for Bonferroni correction. Behavioral Ecology. 2006;17:682– 687. 19 Aniansson A, Grimby G, Hedberg M, et al. Muscle function in old age. Scand J Rehabil Med Suppl. 1978;6:43– 49. 20 Bilodeau M, Erb MD, Nichols JM, et al. Fatigue of elbow flexor muscles in younger and older adults. Muscle Nerve. 2001;24:98 –106. Number 8 21 Bilodeau M, Henderson TK, Nolta BE, et al. Effect of aging on fatigue characteristics of elbow flexor muscles during sustained submaximal contraction. J Appl Physiol. 2001;91:2654 –2664. 22 Chatterjee S, Chowdhuri BJ. Comparison of grip strength and isomeric endurance between the right and left hands of men and their relationship with age and other physical parameters. J Hum Ergol (Tokyo). 1991;20:41–50. 23 Christie A, Kamen G. Motor unit firing behavior during prolonged 50% MVC dorsiflexion contractions in young and older adults. J Electromyogr Kinesiol. 2009;9: 543–552. 24 Griffith EE, Yoon T, Hunter SK. Age and load compliance alter time to task failure for a submaximal fatiguing contraction with the lower leg. J Appl Physiol. 2010; 108:1510 –1519. 25 Hara Y, Findley TW, Sugimoto A, Hanayama K. Muscle fiber conduction velocity (MFCV) after fatigue in elderly subjects. Electromyogr Clin Neurophysiol. 1998;38:427– 435. 26 Huang CT, Huang CC, Young MS, Hwang IS. Age effect on fatigue-induced limb acceleration as a consequence of highlevel sustained submaximal contraction. Eur J Appl Physiol. 2007;100:675– 683. 27 Hunter SK, Rochette L, Critchlow A, Enoka RM. Time to task failure differs with load type when old adults perform a submaximal fatiguing contraction. Muscle Nerve. 2005;31:730 –740. 28 Johnson T. Age-related differences in isometric and dynamic strength and endurance. Phys Ther. 1982;62:985–989. 29 Lanza IR, Befroy DE, Kent-Braun JA. Agerelated changes in ATP-producing pathways in human skeletal muscle in vivo. J Appl Physiol. 2005;99:1736 –1744. 30 Mademli L, Arampatzis A. Mechanical and morphological properties of the triceps surae muscle-tendon unit in old and young adults and their interaction with a submaximal fatiguing contraction. J Electromyogr Kinesiol. 2008;18:89 –98. 31 Mademli L, Arampatzis A, Walsh M. Agerelated effect of static and cyclic loadings on the strain-force curve of the vastus lateralis tendon and aponeurosis. J Biomech Eng. 2008;130:011007. 32 Momen A, Leuenberger UA, Handly B, Sinoway LI. Effect of aging on renal blood flow velocity during static exercise. Am J Physiol Heart Circ Physiol. 2004;287: H735–H740. 33 Petrofsky JS, Burse RL, Lind AR. Comparison of physiological responses of women and men to isometric exercise. J Appl Physiol. 1975;38:863– 868. 34 Petrofsky JS, Lind AR. Aging, isometric strength and endurance, and cardiovascular responses to static effort. J Appl Physiol. 1975;38:91–95. 35 Petrofsky JS, Laymon M. The effect of ageing in spinal cord injured humans on the blood pressure and heart rate responses during fatiguing isometric exercise. Eur J Appl Physiol. 2002;86:479 – 486. August 2011 Age-Related Muscle Fatigue: A Meta-analysis 36 Petrofsky JS, Prowse M, Remigio W, et al. The use of an isometric handgrip test to show autonomic damage in people with diabetes. Diabetes Technol Ther. 2009;11: 361–368. 37 Smolander J, Aminoff T, Korhonen I, et al. Heart rate and blood pressure responses to isometric exercise in young and older men. Eur J Appl Physiol Occup Physiol. 1998;77:439 – 444. 38 Taylor JA, Hand GA, Johnson DG, Seals DR. Sympathoadrenal-circulatory regulation during sustained isometric exercise in young and older men. Am J Physiol. 1991; 261(5 pt 2):R1061–R1069. 39 Yassierli, Nussbaum MA, Iridiastadi H, Wojcik LA. The influence of age on isometric endurance and fatigue is muscle dependent: a study of shoulder abduction and torso extension. Ergonomics. 2007; 50:26 – 45. 40 Yoon T, De-Lap BS, Griffith EE, Hunter SK. Age-related muscle fatigue after a lowforce fatiguing contraction is explained by central fatigue. Muscle Nerve. 2008;37: 457– 466. 41 Allman BL, Rice CL. Perceived exertion is elevated in old age during an isometric fatigue task. Eur J Appl Physiol. 2003;89: 191–197. 42 Allman BL, Rice CL. Incomplete recovery of voluntary isometric force after fatigue is not affected by old age. Muscle Nerve. 2001;24:1156 –1167. 43 Callahan DM, Foulis SA, Kent-Braun JA. Age-related fatigue resistance in the knee extensor muscles is specific to contraction mode. Muscle Nerve. 2009;39:692–702. 44 Chan KM, Raja AJ, Strohschein FJ, Lechelt K. Age-related changes in muscle fatigue resistance in humans. Can J Neurol Sci. 2000;27:220 –228. 45 Chung LH, Callahan DM, Kent-Braun JA. Age-related resistance to skeletal muscle fatigue is preserved during ischemia. J Appl Physiol. 2007;103:1628 –1635. August 2011 46 Ditor DS, Hicks AL. The effect of age and gender on the relative fatigability of the human adductor pollicis muscle. Can J Physiol Pharmacol. 2000;78:781–790. 47 Kent-Braun JA, Ng AV, Doyle JW, Towse TF. Human skeletal muscle responses vary with age and gender during fatigue due to incremental isometric exercise. J Appl Physiol. 2002;93:1813–1823. 48 Lanza IR, Russ DW, Kent-Braun JA. Agerelated enhancement of fatigue resistance is evident in men during both isometric and dynamic tasks. J Appl Physiol. 2004; 97:967–975. 49 Lanza IR, Larsen RG, Kent-Braun JA. Effects of old age on human skeletal muscle energetics during fatiguing contractions with and without blood flow. J Physiol. 2007;583(pt 3):1093–1105. 50 Mademli L, Arampatzis A. Effect of voluntary activation on age-related muscle fatigue resistance. J Biomech. 2008;41: 1229 –1235. 51 Rubinstein S, Kamen G. Decreases in motor unit firing rate during sustained maximal-effort contractions in young and older adults. J Electromyogr Kinesiol. 2005;15:536 –543. 52 Russ DW, Towse TF, Wigmore DM, et al. Contrasting influences of age and sex on muscle fatigue. Med Sci Sports Exerc. 2008;40:234 –241. 53 Stackhouse SK, Stevens JE, Lee SC, et al. Maximum voluntary activation in nonfatigued and fatigued muscle of young and elderly individuals. Phys Ther. 2001;81: 1102–1109. 54 Baudry S, Klass M, Pasquet B, Duchateau J. Age-related fatigability of the ankle dorsiflexor muscles during concentric and eccentric contractions. Eur J Appl Physiol. 2007;100:515–525. 55 Lindstrom B, Lexell J, Gerdle B, Downham D. Skeletal muscle fatigue and endurance in young and old men and women. J Gerontol A Biol Sci Med Sci. 1997;52: B59 –B66. 56 Lindstrom B, Karlsson JS, Lexell J. Isokinetic torque and surface electromyography during fatiguing muscle contractions in young and older men and women. Isokinet Exerc Sci. 2006;14:225–234. 57 McNeil CJ, Rice CL. Fatigability is increased with age during velocitydependent contractions of the dorsiflexors. J Gerontol A Biol Sci Med Sci. 2007; 62:624 – 629. 58 Muller F, Dehail P, Bestaven E, et al. Maximal and sustained isokinetic lower-limb muscle strength in hospitalized older people. Muscle Nerve. 2007;35:739 –744. 59 Rawson ES. Enhanced fatigue resistance in older adults during repeated sets of intermittent contractions. J Strength Cond Res. 2010;24:251–256. 60 Schwendner KI, Mikesky AE, Holt WS Jr, et al. Differences in muscle endurance and recovery between fallers and nonfallers, and between young and older women. J Gerontol A Biol Sci Med Sci. 1997;52: M155–M160. 61 Lexell J, Taylor CC, Sjostrom M. What is the cause of the ageing atrophy: total number, size and proportion of different fiber types studied in whole vastus lateralis muscle from 15- to 83-year-old men. J Neurol Sci. 1988;84:275–294. 62 Allman BL, Rice CL. An age-related shift in the force-frequency relationship affects quadriceps fatigability in old adults. J Appl Physiol. 2004;96:1026 –1032. 63 Raj IS, Bird SR, Shield AJ. Aging and the force-velocity relationship of muscles. Exp Gerontol. 2010;45:81–90. 64 Hortobagyi T, Mizelle C, Beam S, DeVita P. Old adults perform activities of daily living near their maximal capabilities. J Gerontol A Biol Sci Med Sci. 2003;58:M453–M460. Volume 91 Number 8 Physical Therapy f 1165 Research Report Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control: A Randomized Controlled Trial Jeffrey R. Hebert, John R. Corboy, Mark M. Manago, Margaret Schenkman J.R. Hebert, PT, PhD, School of Medicine–Physical Therapy Program, Department of Physical Medicine and Rehabilitation, and Department of Neurology, University of Colorado, Anschutz Medical Campus, Mailstop C-244, 13121 E 17th Ave, ED II South, Room L28 –3133, Aurora, CO 80045 (USA). Address all correspondence to Dr Hebert at: [email protected]. J.R. Corboy, MD, Department of Neurology, University of Colorado, Anschutz Medical Campus. M.M. Manago, PT, DPT, NCS, Physical Therapy, Department of Rehabilitation, University of Colorado Hospital, Aurora, Colorado. M. Schenkman, PT, PhD, FAPTA, School of Medicine–Physical Therapy Program and Department of Physical Medicine and Rehabilitation, University of Colorado, Anschutz Medical Campus. [Hebert JR, Corboy JR, Manago MM, Schenkman M. Effects of vestibular rehabilitation on multiple sclerosis–related fatigue and upright postural control: a randomized controlled trial. Phys Ther. 2011;91:1166 –1183.] © 2011 American Physical Therapy Association Published Ahead of Print: June 16, 2011 Accepted: March 29, 2011 Submitted: November 18, 2010 Background. Fatigue and impaired upright postural control (balance) are the 2 most common findings in people with multiple sclerosis (MS), with treatment approaches varying greatly in effectiveness. Objectives. The aim of this study was to investigate the benefits of implementing a vestibular rehabilitation program for the purpose of decreasing fatigue and improving balance in patients with MS. Design. The study was a 14-week, single-blinded, stratified blocked randomized controlled trial. Setting. Measurements were conducted in an outpatient clinical setting, and interventions were performed in a human performance laboratory. Patients. Thirty-eight patients with MS were randomly assigned to an experimental group, an exercise control group, or a wait-listed control group. Intervention. The experimental group underwent vestibular rehabilitation, the exercise control group underwent bicycle endurance and stretching exercises, and the wait-listed control group received usual medical care. Measurements. Primary measures were a measure of fatigue (Modified Fatigue Impact Scale), a measure of balance (posturography), and a measure of walking (Six-Minute Walk Test). Secondary measures were a measure of disability due to dizziness or disequilibrium (Dizziness Handicap Inventory) and a measure of depression (Beck Depression Inventory–II). Results. Following intervention, the experimental group had greater improvements in fatigue, balance, and disability due to dizziness or disequilibrium compared with the exercise control group and the wait-listed control group. These results changed minimally at the 4-week follow-up. Limitations. The study was limited by the small sample size. Further investigations are needed to determine the underlying mechanisms associated with the changes in the outcome measures due to the vestibular rehabilitation program. Conclusion. A 6-week vestibular rehabilitation program demonstrated both sta- Post a Rapid Response to this article at: ptjournal.apta.org 1166 f Physical Therapy tistically significant and clinically relevant change in fatigue, impaired balance, and disability due to dizziness or disequilibrium in patients with MS. Volume 91 Number 8 August 2011 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control F atigue and limited mobility are among the most common symptoms in people with multiple sclerosis (MS),1 with reports of fatigue ranging from 50% to 85%.2,3 The definition of MS-related fatigue is commonly understood as the selfreported perception of decreased physical or mental energy, often leading to limitations in daily activities or routines.4,5 Multiple sclerosis– related fatigue is strongly linked to impaired physical activity and quality of life.6,7 The cause of fatigue in people with MS most likely is multifactorial,8 including both primary and secondary causes. Primary fatigue is directly related to the disease process involving the neuromuscular system in the form of demyelination or axonal degeneration. Secondary fatigue refers to fatigue indirectly caused by factors such as depression, physical inactivity, or sleep disorder.5 with resulting dizziness or vertigo. Impaired upright postural control has been linked to poor central sensory integration,30 –33 as well as fatigue,34,35 in patients with MS. The high prevalence of MS-related lesions in the brain stem and cerebellum, ranging from 34.7% to 50.9%,36,37 supports the possibility of impairments of central sensory processing, because the brain stem and cerebellum are vital to this process.29,38 – 40 Rates of peripheral deficit vestibulopathy as high as 85% also have been reported in patients with MS,41 further illustrating the importance of the vestibular system for central sensory integration in these patients. Balance training for patients with MS has been reported to improve upright postural control,42,43 although the impact on fatigue has not been tested. Therefore, we postulated that vestibular rehabilitation would be an effective approach to the improvement of both fatigue and upright postural control in patients with MS. The purpose of this investigation was to examine the effects of such a rehabilitation program on fatigue and upright postural control in people with MS. Specifically, we hypothesized that individuals who participate in the vestibular rehabilitation intervention would have significantly reduced self-reported fatigue and significantly improved upright postural control compared with participants in a general exercise program (endurance and stretching program) and participants in a waitlisted control group (usual medical care). The Bottom Line Effective treatment of MS-related fatigue is limited. Drug therapies have been tested, with conflicting reports of efficacy.9,10 Studies of energy conservation education have had conflicting results.11,12 Exercise studies have demonstrated benefits in fitness level,13–15 quality of life,13,15–17 balance,14 and walking capacity13,14,16,18,19 in people with MS; however, no consistent effect on fatigue has been reported. Some multifaceted rehabilitation studies have shown improvements in fatigue,17,20 –23 but others have shown no effect.16 What do we already know about this topic? One possible cause of fatigue worthy of investigation is impairments of central sensory integration. Central sensory integration of the visual, somatosensory, and vestibular systems is the basis for effective upright postural control.24 –29 Impaired central sensory integration can lead to reduced upright postural control, If you’re a patient or caregiver, what might these findings mean for you? August 2011 People with multiple sclerosis (MS) have a multitude of symptoms. Fatigue is the most common complaint, followed by impaired mobility. Balance training is an effective treatment for patients with MS who have impaired upright postural control (ie, balance); however, the evidence for the effectiveness of interventions for MS-related fatigue is limited and inconsistent. Previously, no studies have investigated the effectiveness of a vestibular rehabilitation program on both MS-related fatigue and balance. What new information does this study offer? This study provides early evidence of the feasibility and effectiveness of a vestibular rehabilitation program on fatigue, balance, and disability due to dizziness or disequilibrium for people with MS. If you have MS and have fatigue and balance problems, participation in a program of vestibular rehabilitation may improve fatigue and balance and reduce disability related to dizziness or disequilibrium, with no known side effects. Larger follow-up studies are needed, however, to support these results. Volume 91 Number 8 Physical Therapy f 1167 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Week 1: MFIS, DHI, BDI-II, SOT, 6MWT Baseline Phase (4 wk) Week 2: MFIS,* DHI,* BDI-II* Week 4: MFIS, DHI, BDI-II, SOT, 6MWT Stratified, Blocked Randomized Allocation Exercise Control Group (60-min sessions, twice weekly) Intervention: bicycle ergometry, stretching, fatigue management Week 6: MFIS,* DHI,* BDI-II* Week 6: MFIS,* DHI,* BDI-II* Week 6: MFIS,* DHI,* BDI-II* Week 8: MFIS,* DHI,* BDI-II* Week 8: MFIS,* DHI,* BDI-II* Week 8: MFIS,* DHI,* BDI-II* Week 10: MFIS, DHI, BDI-II, SOT, 6MWT Week 10: MFIS, DHI, BDI-II, SOT, 6MWT Week 10: MFIS, DHI, BDI-II, SOT, 6MWT Week 12: MFIS,* DHI,* BDI-II* Week 12: MFIS,* DHI,* BDI-II* Week 12: MFIS,* DHI,* BDI-II* Week 14: MFIS, DHI, BDI-II, SOT, 6MWT Week 14: MFIS, DHI, BDI-II, SOT, 6MWT Week 14: MFIS, DHI, BDI-II, SOT, 6MWT Follow-up Phase (4 wk) Intervention Phase (6 wk) Experimental Group (60-min sessions, twice weekly) Intervention: vestibular rehabilitation, fatigue management Wait-Listed Control Group (no intervention) Figure 1. Study design schematic. MFIS⫽Modified Fatigue Impact Scale, DHI⫽Dizziness Handicap Inventory, BDI-II⫽Beck Depression Inventory–II, SOT⫽Sensory Organization Test (posturography), 6MWT⫽Six-Minute Walk Test. Asterisk indicates measure administered via telephone. Method Design Overview The study was a 3-arm, 14-week, single-blinded, stratified blocked randomized controlled trial. The study consisted of 3 phases (Fig. 1). All participants underwent 3 outcome measurement sessions during a 4-week, nonintervention baseline phase. They then were randomly assigned to 1 of 3 study arms. There 1168 f Physical Therapy Volume 91 were 2 exercise arms (experimental and exercise control) and a waitlisted control arm. Participants in both exercise groups were treated twice weekly for 6 weeks (intervention phase). All participants then began a 4-week follow-up phase. Participants in the wait-listed control group received treatment consistent with the protocols of this study within the clinical setting upon com- Number 8 pletion of their participation in the study (if they chose to receive the treatment). Setting and Participants Most participants were recruited through clinics at the Rocky Mountain MS Center (RMMSC) at the University of Colorado, Anschutz Medical Campus, Aurora, Colorado. In addition, the RMMSC and the ColoAugust 2011 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control 123 volunteers were assessed for eligibility 85 volunteers were excluded –25 were out of state –5 were out of the metropolitan area –47 did not meet inclusion criteria –8 failed to follow-up for screening 38 participants underwent randomized allocation 12 were assigned to the experimental group 13 were assigned to the exercise control group 13 were assigned to the wait-listed control group No loss to follow-up No loss to follow-up 1 loss to follow-up – Reason: immediately following assignment to wait-listed control group, refused to continue 12 were included in intention-to-treat analysis 13 were included in intention-to-treat analysis 13 were included in intention-to-treat analysis Figure 2. Prospective participant and study participant flow diagram. rado Chapter of the National Multiple Sclerosis Society disseminated information about the study. Over a 33-month period, 123 volunteers were screened for study eligibility (Fig. 2). Inclusion criteria were: 18 to 65 years of age; clinically definite MS; able to walk 100 m with or without August 2011 a single-sided device; a score of ⱖ45 out of 84 on the Modified Fatigue Impact Scale questionnaire10; and a composite score of ⬍72 on the computerized Sensory Organization Test (SOT), demonstrating limited standing balance. Exclusion criteria were: unable to walk; use of pharmacolog- ical agents to control fatigue or that caused fatigue; change in MS-specific disease modification medication within 3 months prior to the study; documented MS-related relapse within 6 months prior to the study; other conditions that may cause fatigue (including depressive and Volume 91 Number 8 Physical Therapy f 1169 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control sleep disorders); impaired upright postural control or limited participation in an exercise program; and participation in a vestibular or endurance exercise program within 8 weeks prior to the study. experimental group and the exercise control group were performed in the same human performance laboratory, with each participant having the same amount of supervision and interaction with the investigator. An SOT composite score of 7.0 as a clinically meaningful difference resulted in a sample size estimate of 30 to achieve 0.80 power at a significance level of .05. The 7.0-point effect size was derived from a previous investigation reporting a 6.7-point effect size indicated a tendency toward statistical significance.44 Oversampling was performed to account for possible dropouts, resulting in 38 as the final study size. Individuals in the experimental group participated in a standardized vestibular rehabilitation program consisting of upright postural control and eye movement exercises (Appendix 1) based on clinical experience and published literature.45,46 Each item was performed for 1 to 2 minutes, for a total of 55 minutes. Specific items were selected for a daily independent home exercise program (HEP), which was assigned throughout the intervention and follow-up phases (Appendix 1). A physical therapist with 5 years of experience evaluating patients with neurological disorders, including MS, performed all outcome measurements in an outpatient clinical setting and was blinded from group assignments. An investigator with 12 years of experience as a physical therapist treating patients with MS implemented all exercise protocols in a human performance laboratory and was blinded from all outcome measurements. All participants gave written informed consent. Randomization and Interventions Following the baseline phase, 2 strata were formed based on the most recent magnetic resonance imaging report: participants with and without brain-stem or cerebellar neurological involvement. Block sizes of 3 were randomly selected for each strata. A clinician not involved in the study concealed the block sequences and provided the random group assignments. Participants then were randomly allocated to 1 of 3 arms: an experimental group, an exercise control group, or a waitlisted control group. All supervised intervention sessions in both the 1170 f Physical Therapy Volume 91 The exercise control group participated in endurance and stretching exercises. To account for a possible abnormally low heart rate response to exercise (blunted heart rate response) frequently observed in patients with MS, participants in the exercise control group first performed a submaximal modified YMCA cycle ergometry graded exercise test (GET) (Appendix 2).47 Peak heart rate (HRpeak), which was the highest value of heart rate at the time of symptom-limiting GET termination, served as the value for endurance exercise intensity prescription. The endurance exercise consisted of stationary bicycling: 5-minute warmup, two 15-minute sessions; and 2- to 5-minute cool-down. The training intensity during the 15-minute sessions was 65% to 75% of HRpeak; 11 to 14 (moderate intensity of exertion) on the Borg Rating of Perceived Exertion (RPE) Scale, ranging from 6 (“no exertion at all”) to 20 (“maximal exertion”); and constant pedal rate of 50 rpm. The level of intensity and duration of cycling were based on the typical capacity of individuals with MS and recommendations in Number 8 the literature.47 The stretching exercises included stretches of the following muscles: gastrocnemiussoleus, quadriceps, hamstrings, gluteus maximus, and iliopsoas and rectus femoris. Stretches were held for 30 seconds. A daily independent HEP was assigned throughout the intervention and follow-up phases. The HEP included the stretching exercises and stationary bicycling or an alternative activity (eg, walking) at levels consistent with the supervised training sessions. Both exercise groups received the same 5-minute fatigue management education. Included were discussions of: daily rest intervals, selfmonitoring of exertion levels, work station ergonomics, and heat intolerance education. A daily log was issued to each individual in the exercise groups to record adherence to the HEP and fatigue management components. Outcomes and Follow-up Primary outcome measures. Selfreported fatigue was measured using the 21-item Modified Fatigue Impact Scale (MFIS). The MFIS is reported to be a reliable and valid measure for patients with MS.4 Responses are scored from 0 to 4, with total scores ranging from 0 to 84 and with higher scores indicating a larger impact of fatigue. Static upright postural control was measured using a posturography test (ie, Sensory Organization Test [SOT]), which has been used in prior studies to illustrate balance disorders in people with MS.30,31,42 The Smart Balance Master System* was used for this test. This test assesses upright postural control during 6 different conditions of sensory feedback. Postural sway is recorded and converted * NeuroCom International Inc, 9570 SE Lawnfield Rd, Clackamas, OR 97015. August 2011 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control to a percentage of equilibrium (composite score). Walking capacity was measured using the Six-Minute Walk Test (6MWT), which has been used measure functional exercise capacity in this population.48 Standard instructions and testing guidelines were implemented.49 Distance (in feet)† was recorded. Secondary outcome measures. Self-reported disability due to dizziness or disequilibrium was measured using the 25-item Dizziness Handicap Inventory (DHI). Each item has 3 responses: “yes,” “sometimes,” and “no.” Total scores range from 0 to 100, with higher scores indicating greater disability due to dizziness or disequilibrium. The DHI has high reliability and discriminates “fallers” from “nonfallers” in the MS population.50 Self-reported depression was measured using the 21-item Beck Depression Inventory–II (BDI-II).51 Each item has 4 responses, with the total score ranging from 0 (“no depression”) to 63 (“greatest depression”). The MFIS, DHI, and BDI-II were administered 8 times throughout the study, and the SOT and 6MWT were administered 4 times (Fig. 1). Data from the baseline phase were averaged to provide a point estimate for the 4 weeks prior to the intervention phase. Outcome measure analyses occurred at the end of the intervention phase (baseline to 10-week follow-up) and at the end of the follow-up phase (10-week follow-up to 14-week follow-up). Data Analysis All outcome measures were analyzed as continuous data. One-way analysis of variance was used for multigroup comparisons of preintervention and † 1 ft⫽0.3048 m. August 2011 postintervention data and of postintervention to end of follow-up data for each outcome variable and for multigroup comparisons of time duration in the study. Prior to performing post hoc, pair-wise comparisons, a robust test of equality of means (ie, the Welch statistic) was performed to verify the valid application of a Bonferroni correction method. Outcome measures that underwent multigroup Bonferroni correction met the statistical significance of equality of means (P⬍.05). For within-group comparisons of preintervention and postintervention data and of postintervention to end of follow-up data, the paired t test was used. For experimental group and exercise control group comparisons of adherence to the HEP and fatigue management, the independent t test was used. The Fisher exact test was used for baseline analysis of nominal data.52 Correlational analyses were performed to test the relationship between mean changes in MFIS total score, SOT composite score, and DHI total score for the combined study sample from baseline to the end of the intervention phase and from baseline to the end of the follow-up phase. The Pearson product moment correlation coefficient test was used for the analysis of associations. All tests were 2-tailed, using .05 as the level of statistical significance. Standard deviations and 95% confidence intervals (CIs) also were calculated. The numeric difference in change of outcome measure between groups is presented as effect size. Standardized difference of the mean (SDM) was calculated based on Cohen d standard effect size index: small (SDM: ⱕ0.2), medium (SDM: ⬎0.2 but ⱕ0.7), and large (SDM: ⱖ0.8 to 2.0).53–55 Event rates for each group and the subsequent number needed to treat are presented for the primary outcome measures of fatigue (MFIS total score) and upright postural con- trol (SOT composite score). A change in the MFIS total score of ⱖ15.010 and a change in the SOT composite score of ⱖ7.044 were used as the meaningful changes and cutoff scores for event rate calculations. Intention-to-treat analysis was implemented to address any loss to followup. The average of the group change for each outcome measure at each analysis period served as the value applied to data missing from loss to follow-up. Unless otherwise stated, statistical analyses were performed using SPSS for Windows, version 17.0.‡ Role of the Funding Source This study was partially supported by the National Multiple Sclerosis Society (NMSS) (Pilot Project no. PP1501), which approved the design of the study, but did not control the conduct of the research team, including recruitment, patient participation, data analyses, and manuscript preparation. Results Characteristics of the sample, including demographic data and baseline data for the outcome measures, are presented in Table 1. No differences were found among the 3 groups. Primary and Secondary Outcomes (Baseline to 10 Weeks) We first examined differences in the primary and secondary outcomes following the 6-week intervention phase (baseline to 10 weeks). These data are depicted in Table 2. Fatigue. As hypothesized, the experimental group demonstrated significant improvement in MFIS total score (Tab. 2). Groups were significantly different on MFIS total score (P⫽.004), with the experimen‡ SPSS Inc, 233 S Wacker Dr, Chicago, IL 60606. Volume 91 Number 8 Physical Therapy f 1171 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Table 1. Baseline Demographics and Characteristicsa Experimental Group (nⴝ12) Variable Age (y) 46.8 (10.5) Sex, female/male 9/3 MS diagnosis duration (y) 6.5 (5.6) Exercise Control Group (nⴝ13) 42.6 (10.4) 11/2 5.1 (3.2) Wait-Listed Control Group (nⴝ13) P 50.2 (9.2) .175b 11/2 .767c 9.1 (7.3) .206b 1.00c MS diagnosis subtype Relapsing-remitting Secondary progressive 11 11 12 1 2 1 1.00c MS-related lesion location Non-brain stem/cerebellar 4 4 4 Brain stem/cerebellar 8 9 9 51.0 (6.8) 51.0 (8.6) 55.9 (11.6) 1,335.6 (320.3) 1,066.1 (335.9) MFIS total score 6MWT (ft) 1,049.2 (328.9) .312b .066b SOT composite score (%) 60.2 (14.0) 50.3 (16.3) 59.5 (12.1) .164b BDI-II total score 16.5 (9.1) 17.3 (8.6) 18.5 (6.4) .817b DHI total score 48.0 (10.7) 47.0 (12.1) 56.4 (14.6) .132b a Values expressed as means (SD), except for sex, MS diagnosis subtype, and MS-related lesion location, which are expressed as nominal counts. MS⫽multiple sclerosis, MFIS⫽Modified Fatigue Impact Scale, 6MWT⫽Six-Minute Walk Test, SOT⫽Sensory Organization Test, BDI-II⫽Beck Depression Inventory–II, DHI⫽Dizziness Handicap Inventory. b P values assessed by one-way analysis of variance. c P values assessed by Fisher exact test. tal group’s improvement significantly greater than that of the exercise control group (P⫽.024) and the wait-listed control group (P⫽.005). No difference was found between the exercise control group and the wait-listed control group (P⫽1.00). Large MFIS total score SDMs were found for the experimental group compared with the exercise control group (d⫽1.06) and the wait-listed control group (d⫽1.33), and the difference in MFIS total score SDMs between the exercise control group and the wait-listed control group was minimal (d⫽0.24). Based on 67% of the experimental group, 23% of the exercise control group, and 15% of the wait-listed control group improving on the MFIS by ⱖ15.0, the number needed to treat was 2.3 when comparing the experimental group with the exercise control group and 1.9 when comparing the experimental group with the control group. 1172 f Physical Therapy Volume 91 Upright postural control. As hypothesized, the experimental group improved significantly in the SOT composite score (Tab. 2). There was a significant difference among the groups (P⬍.001). The experimental group showed significant improvement compared with the exercise control group (P⫽.001) and the wait-listed control group (P⫽.003). No difference was found between the exercise control group and the wait-listed control group (P⫽1.00). Large SOT composite score SDMs were found for the experimental group compared with the exercise control group (d⫽1.37) and the wait-listed control group (d⫽1.28), and the difference in SOT composite score SDMs between the exercise control group and the waitlisted control group was minimal (d⫽0.21). Based on 92% of the experimental group and 38% of both the exercise control group and the waited-listed control group improv- Number 8 ing on the SOT by ⱖ7.0, the number needed to treat was 1.9. Self-reported disability due to dizziness or disequilibrium. The experimental group improved significantly in DHI total score, whereas the other groups failed to improve (Tab. 2). Groups were significantly different (P⫽.005) at the end of the intervention phase; the experimental group’s improvement was significant compared with that of the exercise control group (P⫽.018) and the wait-listed control group (P⫽.009). No difference was found between the exercise control and wait-listed control groups (P⫽1.00). Large DHI total score SDMs were found for the experimental group compared with the exercise control group (d⫽1.03) and the wait-listed control group (d⫽1.12), and the difference in DHI total score SDMs between the exercise control group and the wait-listed August 2011 August 2011 P Volume 91 P Number 8 1,066.1 (335.9) P .092 .345 46.0 (168.7) ⫺56.0 to 148.0 85.1 (159.5) ⫺16.3 to 186.4 95% CI 1,112.1 (391.3) Change in 6MWT 1,335.6 (320.3) 1,420.7 (283.6) End of intervention phase .415 Baseline 6MWT .010 ⫺2.2 (9.5) ⫺8.0 to 3.5 ⫺31.9 to ⫺5.5 ⫺18.7 (20.7) 95% CI Change in DHI 44.8 (11.6) 48.0 (10.7) 29.3 (18.6) End of intervention phase 47.0 (12.1) .011 ⬍.001 Baseline DHI 5.2 (6.2) 1.4 to 8.9 18.5 (12.3) Change in SOT 55.5 (14.9) 50.3 (16.3) 10.7 to 26.3 78.7 (6.0) 95% CI 60.2 (14.0) .085 ⬍.001 End of intervention phase ⫺6.7 (12.9) ⫺14.5 to 1.1 ⫺21.5 (15.0) ⫺31.1 to ⫺11.9 Baseline SOT P 95% CI Change in MFIS 44.3 (16.4) 51.0 (6.8) 29.5 (15.8) End of intervention phase 51.0 (8.6) Exercise Control Group (nⴝ13)b Baseline MFIS Outcome Measure Experimental Group (nⴝ12)b .378 ⫺30.9 to 75.6 22.4 (88.1) 1,071.6 (375.0) 1,049.2 (328.9) .821 ⫺6.4 to 5.2 ⫺0.6 (9.6) 55.8 (20.9) 56.4 (14.6) .001 3.2 to 9.5 6.4 (5.2) 65.9 (14.5) 59.5 (12.1) .255 ⫺10.6 to 3.1 ⫺3.8 (11.4) 52.1 (17.1) 55.9 (11.6) Wait-Listed Control Group (nⴝ13)b 1.00 ⫺104.8 to 182.9 39.1 .018 2.3 to 30.6 16.5 .001 4.9 to 21.8 13.3 .024 1.6 to 28.0 14.8 Effect Sizec 0.24 1.03 1.37 1.06 Effect Size Index (d) Experimental Group Compared With Exercise Control Group .842 ⫺81.1 to 206.5 62.7 .009 3.9 to 32.2 18.1 .003 3.7 to 20.5 12.1 .005 4.5 to 30.9 17.7 Effect Sizec 0.49 1.12 1.28 1.33 Effect Size Index (d) Experimental Group Compared With WaitListed Control Group 1.00 ⫺117.3 to 164.5 23.6 1.00 ⫺12.3 to 15.5 1.6 1.00 ⫺7.0 to 9.5 ⫺1.2 1.00 ⫺10.0 to 15.9 2.9 Effect Sizec (Continued) 0.18 0.17 ⫺0.21 0.24 Effect Size Index (d) Exercise Control Group Compared With WaitListed Control Group Fatigue, Upright Postural Control, Disability Due to Dizziness or Disequilibrium, Walking Capacity, and Depression: Baseline to End of Intervention Phase (10 Weeks)a Table 2. Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Physical Therapy f 1173 .431 .101 .003 .001 P a Baseline, end of intervention phase, and change in outcome measure values expressed as mean (SD), 95% CI⫽95% confidence interval. Effect size⫽numeric difference in change of outcome measure among groups. Effect size index (d)⫽Cohen d standard effect size index. MFIS⫽Modified Fatigue Impact Scale total score; SOT⫽Sensory Organization Test, composite score (percentage); DHI⫽Dizziness Handicap Inventory total score; 6MWT⫽Six-Minute Walk Test score (feet); BDI-II⫽Beck Depression Inventory–II total score. b Within-group comparison of change in outcome measure (paired t test). c Between-group comparison of change in outcome measure (post hoc pair-wise comparisons following one-way analysis of variance). 1.00 .307 0.6 ⫺6.8 to 7.8 0.60 5.0 0.70 ⫺3.0 to 11.9 4.4 ⫺4.5 (9.2) ⫺10.1 to 1.1 ⫺5.1 (4.9) ⫺8.0 to ⫺2.1 ⫺9.5 (7.4) ⫺14.2 to ⫺4.8 14.0 (9.0) 12.2 (6.5) Change in BDI-II 18.5 (6.4) 17.3 (8.6) 16.5 (9.1) 7.0 (7.3) End of intervention phase Baseline BDI-II 95% CI Effect Sizec Exercise Control Group (nⴝ13)b Physical Therapy Outcome Measure Experimental Group (nⴝ12)b f Continued Table 2. 1174 ⫺2.5 to 12.4 Effect Sizec Effect Sizec 0.08 Effect Size Index (d) Effect Size Index (d) Effect Size Index (d) Wait-Listed Control Group (nⴝ13)b Experimental Group Compared With Exercise Control Group Experimental Group Compared With WaitListed Control Group Exercise Control Group Compared With WaitListed Control Group Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Volume 91 Number 8 control group (d⫽0.17). was negligible Depression. Table 2 illustrates that depression, based on the BDI-II scores, improved significantly in the experimental group and the exercise control group, but not in the waitlisted control group. However, changes were not considerably different among the groups (P⫽.202). Walking capacity. Walking capacity, as measured by the 6MWT, improved in all groups (Tab. 2); however, within-group changes were neither significant nor different among the groups (P⫽.549). Primary and Secondary Outcomes (10 Weeks to 14 Weeks) We next examined the results of the 4-week follow-up phase. Table 3 presents group changes for the MFIS, SOT, DHI, and 6MWT for the follow-up period between week 10 and week 14. Within-group changes were insignificant, with the exception of the BDI-II. The wait-listed control group increased in depression (X⫽2.6, SD⫽3.2; P⫽.011); however, changes in BDI-II scores were not significantly different among the groups (P⫽.309). Ancillary Analyses Relationship of the changes in outcome measures. We next tested for relationships between changes in the primary outcome measures of fatigue and upright postural control and the main secondary outcome measure of disability due to dizziness or disequilibrium. A correlational analysis was performed on the total study sample (N⫽38) to compare the changes from baseline to the end of the intervention phase and from baseline to the follow-up phase. The MFIS total score mean change had a significant inverse relationship August 2011 August 2011 .880 .867 .280 ⫺0.4 (3.9) ⫺2.8 to 2.1 .770 Change in SOT 95% CI Volume 91 Number 8 .509 ⫺24.6 (112.1) ⫺95.8 to 46.7 Change in 6MWT 95% CI .463 ⫺58.2 (308.5) ⫺244.7 to 128.2 1,396.1 (330.5) P 1,053.9 (448.7) 1,420.7 (283.6) End of follow-up phase 1,112.1 (391.3) .590 .507 .348 ⫺47.8 to 125.7 38.9 (143.6) 1,110.5 (284.0) 1,071.6 (375.0) .144 ⫺0.7 to 4.1 1.7 (3.9) ⫺1.3 (8.0) ⫺6.1 to 3.6 3.5 (17.7) End of intervention phase 6MWT P 95% CI 57.5 (19.9) 55.8 (20.9) .524 ⫺2.3 to 4.3 1.0 (5.5) 66.9 (14.3) 65.9 (14.5) .819 ⫺3.8 to 4.8 0.5 (7.1) 52.6 (17.4) 52.1 (17.1) 43.5 (14.5) ⫺7.7 to 14.7 32.8 (24.5) End of follow-up phase Change in DHI 29.3 (18.6) End of intervention phase DHI 44.8 (11.6) 2.3 (7.4) ⫺2.1 to 6.8 78.3 (4.9) P 57.8 (16.5) 78.7 (6.0) End of follow-up phase 55.5 (14.9) 0.4 (9.0) ⫺5.0 to 5.8 0.8 (15.1) End of intervention phase SOT P 95% CI 44.7 (16.3) 44.3 (16.4) Exercise Control Group (nⴝ13)b ⫺8.9 to 10.4 30.3 (20.8) End of follow-up phase Change in MFIS 29.5 (15.8) End of intervention phase MFIS Outcome Measure Experimental Group (nⴝ12)b Wait-Listed Control Group (nⴝ13)b 1.00 ⫺176.7 to 244.0 33.6 .895 ⫺16.0 to 6.5 ⫺4.8 .787 ⫺8.5 to 3.2 ⫺2.7 1.00 ⫺11.3 to 10.5 ⫺0.4 Effect Sizec 0.14 ⫺0.35 ⫺0.46 ⫺0.03 Effect Size Index (d) Experimental Group Compared With Exercise Control Group 1.00 ⫺273.8 to 146.8 ⫺63.5 1.00 ⫺13.1 to 9.5 ⫺1.8 1.00 ⫺7.2 to 4.5 ⫺1.4 1.00 ⫺11.3 to 10.5 ⫺0.3 Effect Sizec ⫺0.49 ⫺0.14 ⫺0.29 ⫺0.03 Effect Size Index (d) Experimental Group Compared With Wait-Listed Control Group .731 ⫺303.2 to 108.9 ⫺97.1 1.00 ⫺8.1 to 14.0 3.0 1.00 ⫺4.4 to 7.0 1.3 1.00 ⫺10.6 to 10.7 0.1 Effect Sizec (Continued) ⫺0.40 0.48 0.20 0.01 Effect Size Index (d) Exercise Control Group Compared With Wait-Listed Control Group Fatigue, Upright Postural Control, Disability Due to Dizziness or Disequilibrium, Walking Capacity, and Depression: End of Intervention Phase (10 Weeks) to End of Follow-up Phase (14 Weeks)a Table 3. Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Physical Therapy f 1175 ⫺0.27 ⫺2.0 Physical Therapy ⫺4.2 to 8.1 1.00 1.00 ⫺10.2 to 2.4 .385 .011 .477 .141 0.7 to 4.5 ⫺1.4 to 2.8 ⫺1.8 to 11.0 a 95% CI P 16.6 (9.6) ⫺3.9 0.7 (3.4) 12.9 (8.0) 11.6 (12.3) 4.6 (10.0) Change in BDI-II End of follow-up phase 14.0 (9.0) End of intervention phase 12.2 (6.5) 7.0 (7.3) Outcome Measure BDI-II Experimental Group (nⴝ12)b 2.6 (3.2) ⫺0.52 ⫺8.3 to 4.3 1.9 Effect Sizec Effect Size Index (d) Effect Sizec Wait-Listed Control Group (nⴝ13)b Exercise Control Group (nⴝ13)b f Continued Table 3. 1176 End of intervention phase, end of follow-up phase, and change in outcome measure values expressed as mean (SD), 95% CI⫽95% confidence interval. Effect size⫽numeric difference in change of outcome measure between groups. Effect size index (d)⫽Cohen d standard effect size index. MFIS⫽Modified Fatigue Impact Scale total score; SOT⫽Sensory Organization Test, composite score (percentage); DHI⫽Dizziness Handicap Inventory total score; 6MWT⫽Six-Minute Walk Test score (feet); BDI-II⫽Beck Depression Inventory–II total score. b Within-group comparison of change in outcome measure (paired t test). c Between-group comparison of change in outcome measure (post hoc pair-wise comparisons following one-way analysis of variance). Effect Size Index (d) Effect Size Index (d) Effect Sizec 0.58 Exercise Control Group Compared With Wait-Listed Control Group Experimental Group Compared With Exercise Control Group Experimental Group Compared With Wait-Listed Control Group Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Volume 91 Number 8 to SOT composite score mean change at the end of the intervention phase (r⫽⫺.41, P⫽.011) and the end of the follow-up phase (r⫽⫺.56, P⬍.001). Additionally, the MFIS total score mean change had a significant direct relationship to DHI total score mean change at the end of the intervention phase (r⫽.67, P⬍.001) and at the end of the follow-up phase (r⫽.76, P⬍.001). Lastly, the DHI total score mean change had a significant inverse correlation to SOT composite score mean change at the end of the intervention phase (r⫽⫺.51, P⫽.001) and at the end of the follow-up phase (r⫽⫺.38, P⫽.020). Group equality following randomized allocation. We also examined the length of time in the study for each group and adherence to the HEP and fatigue management by the experimental and exercise control groups. The experimental group’s duration in the study (ie, 16.3 weeks) was not significantly different from that of the other groups; however, the exercise control group’s duration in the study (ie, 17.5 weeks) was different from that of the wisting-list control group (ie, 15.3 weeks) (95% CI⫽0.2 to 4.2, P⫽.025). Each of the exercise groups had 4 participants who did not return their daily log. Of the remaining participants, those in the experimental group had greater adherence to their HEP compared with those in the exercise control group (average of 60.5 and 42.7 days, respectively) (95% CI⫽4.5 to 31.2, P⫽.012). The difference in adherence to fatigue management was negligible: 34.3 days in the experimental group and 25.9 days in the exercise control group (95% CI⫽⫺8.9 to 25.6, P⫽.319). Adverse Events One participant in the exercise control group incurred a minor ankle August 2011 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control sprain during a session. This incident did not require medical care and did not limit continued participation. After being randomly allocated to the wait-listed control group, one individual dropped out of the study due to unhappiness with group assignment. Discussion Findings from this study demonstrate the feasibility of a vestibular rehabilitation program and its effectiveness on fatigue (MFIS total score), upright postural control (SOT composite score), and disability due to dizziness or disequilibrium (DHI total score). The improvements found were significantly greater for participants in the experimental group (who underwent a vestibular rehabilitation program) than for participants in either the exercise control group (who underwent an endurance and stretching program) or the waitlisted control group. The main variable of interest was fatigue, with the results showing that the experimental group was the only group to improve. The improvement of ⫺21.5 points (P⬍.001) in MFIS total score was significant and exceeded previous reports from multifaceted rehabilitation studies: 12-week program (⫺13.0 points, P⫽.02),21 4-week program (⫺15.5 points, P⫽.001),22 and 8-week program (⫺4.0 points, P⫽.64).14 In contrast, the changes in MFIS total scores for both the exercise control group and the wait-listed control group were minimal and statistically similar. The large effect sizes found for the experimental group met the clinically relevant difference of 15.0 points.10 The limited improvement in fatigue found for the exercise control group is comparable to previous findings of several studies that investigated the possible effect of aerobic training on fatigue.13–15,56 August 2011 The second variable of interest was upright postural control. Changes in SOT composite scores for the exercise control group and the wait-listed control group were minimal and statistically similar. These changes are consistent with known learning effect found in a population of healthy individuals; an improvement of 8.0 indicates a true treatment effect.57 In the current study, 2 baseline measurements were conducted to account for learning effect. The experimental group demonstrated a significant improvement in SOT composite score of 18.5 (P⬍.001), which is greater than the score of 14.8 (P⫽.001) reported by Badke et al,58 who investigated the implementation of a vestibular and balance-related rehabilitation program involving a “mixed and central vestibular dysfunction” group. More importantly, the experimental group’s improvement was significantly greater compared with that of the exercise control and waiting-list control groups. The third major finding of this study was that the experimental group was the only group to improve significantly in disability due to dizziness or disequilibrium, with large effect sizes. The improvement in DHI total score of ⫺18.7 points (P⫽.010) is greater than the improvement of ⫺14.3 points (P⫽.02) reported by Badke et al.58 This study was not designed to test the underlying reasons for the improvements in fatigue, upright postural control, and disability due to dizziness or disequilibrium. However, the conceptual framework that led to our investigation may provide insight into the theoretical reasoning. The balance training portion of the vestibular rehabilitation program can be seen as an attempt to condition the central nervous system to provide efficient upright postural control while performing tasks in standing and walking. Moderate to strong associations were found among the changes in fatigue, upright postural control, and disability due to dizziness or disequilibrium. Because both postural control and dizziness reflect central processing, these correlations lend further support to the proposition that impairments of central sensory processing contribute to fatigue in people with MS. Furthermore, these findings suggest that changes in one of these variables could potentially have a coupled reaction in one or both of the other variables. Demyelination and axonal degeneration found in patients with MS often result in impaired motor control,59 with evidence of partial spontaneous neural repair, including axonal and dendritic collateral sprouting.60,61 This neural plasticity has been shown to be enhanced in patients with MS following task-specific rehabilitation training.62– 65 With this knowledge, it can be theorized that vestibular rehabilitation provides the necessary task-specific stimuli for neural reorganization, fostering central sensory integration and resulting in improved upright postural control. Ocular motor training, in the form of eye movement exercises, plays a key role in neuromuscular reorganization.66 Abnormal eye movements are strongly associated with advanced disability in patients with MS.67– 69 Because visual feedback plays a key role in coordinated limb movement,70 it is possible the eye movement exercises included in the vestibular rehabilitation program contributed to the improved postural control found in the experimental group. Peripheral physiological changes also may be involved, including Volume 91 Number 8 Physical Therapy f 1177 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control improved muscle endurance due to repetitive balance training. Improved muscular function may assist in lessening the negative effects of motor fatigue on anticipatory postural adjustments.71 Because of impaired central sensory processing mechanisms, people with MS may require increased conscious or mental attention while performing daily upright tasks. This increase in attention could be an important reason for elevated perception of fatigue in these individuals. This concept is supported by Filippi et al,72 who found that patients with MS who reported greater levels of fatigue had elevated brain activity in the areas devoted to attentional tasks and lower activity in the motor planning and execution regions. Taken together, findings from this investigation support the theory that fatigue in patients with MS is linked to impairments of central sensory integration. Specifically, an intervention program, based on principles of rehabilitation for individuals with vestibular dysfunction and impaired sensorimotor integration, improved upright postural control and fatigue. We also measured depression and walking capacity, both of which changed marginally. Depression in patients with MS has been found to be associated with fatigue,73 with a recent investigation showing a weaker relationship.74 We found that both exercise groups improved in self-reported depression; however, the change was not significantly different between the groups. The lack of significant change in depression following exercise performance is comparable to previous reports.75 Additionally, it should be noted that severe depression was an exclusion criterion, potentially attenuating our findings. 1178 f Physical Therapy Volume 91 At baseline, the experimental group appeared to have had a greater walking capacity, based on the 6MWT scores, compared with the exercise control and wait-listed control groups; however, these differences were not significant and were comparable to the range reported previously in people with MS (670 –1,978 ft).76 –78 The 85.1-foot improvement on the 6MWT by the experimental group is greater than that reported by Rampello and colleagues14 (32.8 ft, P⫽.17) following an 8-week “neurological rehabilitation” program; however, this improvement also was found to be insignificant (P⫽.092). Considering this information and the significant findings for fatigue, upright postural control, and disability due to dizziness or disequilibrium in our study, the 6MWT may not be appropriate for detecting dynamic upright postural control changes in this population and more specifically for this exercise-based investigation. Changes between the 10-week and 14-week periods (Tab. 3) suggest that the outcome measure scores remained stable for 4 weeks following the intervention phase; however, a larger-scale study with a longer follow-up is needed to improve the validity of concluding long-term benefit retention. Lastly, it should be noted that the 2 training groups were different with respect to duration of time in the study and adherence to HEP and fatigue management. However, the differences were not statistically significant, nor were they sufficiently large to be confounding from a clinical perspective. Limitations should be acknowledged. The sample size was too small to permit comparisons between patients with and without brain-stem and cerebellar lesions. Additionally, smaller samples have large variance, although in our study the clinical dif- Number 8 ferences were sufficient that the variances were not a problem for the major outcomes. We chose to include the same fatigue management education in the exercise groups in order to avoid unequal attention to discussions of the typical approach to management of MS-related fatigue. The fact that the exercise control group’s change in all outcome measures was statistically similar compared with the waitlisted control group and that reported adherence to fatigue management was similar between the experimental and exercise control groups illustrates that the education approach in this study was not effective; providing further support for the isolated effects of vestibular rehabilitation found in the experimental group. Based on the findings from this investigation, several issues should be examined in future studies. Specifically, these findings should be replicated in a larger sample with comparisons between individuals who have brain-stem and cerebellar lesions and those without these lesions. Furthermore, analyses should examine other factors that predict which other patients are most likely to respond to such an intervention. Finally, more-specific measures of vestibular and eye movement functions, such as video-oculography,79 should be included in order to investigate underlying mechanisms. Conclusion Findings from this study provide strong evidence supporting the effectiveness of vestibular rehabilitation for the treatment of people with MS who have deficits of fatigue and upright postural control. The large treatment effects occurred after a relatively short intervention period, and changes after 4 weeks of supervised intervention were small, suggesting that vestibular rehabilitation August 2011 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control is a viable treatment option for patients with MS who experience fatigue and impaired upright postural control. Dr Hebert, Dr Corboy, and Dr Schenkman provided concept/idea/research design, project management, and fund procurement. All authors provided writing. Dr Hebert and Dr Manago provided data collection and data analysis. Dr Corboy provided participants. Dr Schenkman provided facilities/equipment. Dr Corboy and Dr Schenkman provided institutional liaisons. Dr Manago provided clerical support. Dr Corboy and Dr Manago provided consultation (including review of manuscript before submission). The authors thank the Rocky Mountain MS Center, Anschutz Medical Campus, Aurora, Colorado, and the Colorado Chapter of the National Multiple Sclerosis Society for assistance in recruitment for this study. A Colorado Multiple Institutional Review Board approved this study. This study was partially supported by the National Multiple Sclerosis Society, Pilot Project no. PP1501. Trial registration: ClinicalTrials.gov Identifier: NCT01216137. DOI: 10.2522/ptj.20100399 References 1 Aronson KJ, Cleghorn G, Goldenberg E. Assistance arrangements and use of services among persons with multiple sclerosis and their caregivers. Disabil Rehabil. 1996;18:354 –361. 2 Putzki N, Katsarava Z, Vago S, et al. Prevalence and severity of multiple-sclerosis– associated fatigue in treated and untreated patients. Eur Neurol. 2008;59:136 –142. 3 Ford H, Trigwell P, Johnson M. The nature of fatigue in multiple sclerosis. J Psychosom Res. 1998;45(1 Spec. 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Extended outpatient rehabilitation: its influence on symptom frequency, fatigue, and functional status for persons with progressive multiple sclerosis. Arch Phys Med Rehabil. 1998;79:141–146. 21 McCullagh R, Fitzgerald AP, Murphy RP, Cooke G. Long-term benefits of exercising on quality of life and fatigue in multiple sclerosis patients with mild disability: a pilot study. Clin Rehabil. 2008;22:206 – 214. 22 Kos D, Kerckhofs E, Nagels G, et al. Assessing fatigue in multiple sclerosis: Dutch modified fatigue impact scale. Acta Neurol Belg. 2003;103:185–191. 23 Judica E, Martinelli Boneschi F, Ungaro D, et al. Impact of fatigue on the efficacy of rehabilitation in multiple sclerosis. J Neurol. 2011 January 15 [Epub ahead of print]. 24 Grigorova V, Ivanov I, Stambolieva K. Effect of sensory inputs alteration and central sensory disinteraction on postural sway and optokinetic reflex maintaining simultaneously body balance. Acta Physiol Pharmacol Bulg. 2001;26:177–180. 25 Grigorova V, Stambolieva K, Ikonomov R. Sensory inputs contribution to vestibuloocular reflex and postural response maintaining simultaneously body balance. Acta Physiol Pharmacol Bulg. 2001;26:181– 184. 26 Bacsi AM, Colebatch JG. Evidence for reflex and perceptual vestibular contributions to postural control. Exp Brain Res. 2005;160:22–28. 27 Keshner EA, Cohen H. Current concepts of the vestibular system reviewed: 1. The role of the vestibulospinal system in postural control. Am J Occup Ther. 1989;43: 320 –330. 28 Cohen H, Keshner EA. Current concepts of the vestibular system reviewed: 2. Visual/vestibular interaction and spatial orientation. Am J Occup Ther. 1989;43:331– 338. 29 Horak FB, Hlavacka F. Somatosensory loss increases vestibulospinal sensitivity. J Neurophysiol. 2001;86:575–585. 30 Jackson RT, Epstein CM, De l’Aune WR. Abnormalities in posturography and estimations of visual vertical and horizontal in multiple sclerosis. Am J Otol. 1995;16:88 – 93. 31 Williams NP, Roland PS, Yellin W. Vestibular evaluation in patients with early multiple sclerosis. Am J Otol. 1997;18:93–100. 32 Rougier P, Faucher M, Cantalloube S, et al. How proprioceptive impairments affect quiet standing in patients with multiple sclerosis. Somatosens Mot Res. 2007;24: 41–51. 33 Nelson SR, Di Fabio RP, Anderson JH. Vestibular and sensory interaction deficits assessed by dynamic platform posturography in patients with multiple sclerosis. Ann Otol Rhinol Laryngol. 1995;104:62– 68. 34 Chung LH, Remelius JG, Van Emmerik RE, Kent-Braun JA. Leg power asymmetry and postural control in women with multiple sclerosis. Med Sci Sports Exerc. 2008;40: 1717–1724. 35 Van Emmerik RE, Remelius JG, Johnson MB, et al. Postural control in women with multiple sclerosis: effects of task, vision and symptomatic fatigue. Gait Posture. 2010;32:608 – 614. 36 Bansil S, Singhal BS, Ahuja GK, et al. Comparison between multiple sclerosis in India and the United States: a case-control study. Neurology. 1996;46:385–387. Volume 91 Number 8 Physical Therapy f 1179 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control 37 Versino M, Colnaghi S, Callieco R, et al. Vestibular evoked myogenic potentials in multiple sclerosis patients. Clin Neurophysiol. 2002;113:1464 –1469. 38 Manzoni D. The cerebellum may implement the appropriate coupling of sensory inputs and motor responses: evidence from vestibular physiology. Cerebellum. 2005;4:178 –188. 39 Devor A. The great gate: control of sensory information flow to the cerebellum. Cerebellum. 2002;1:27–34. 40 Peterson BW, Houk JC. A model of cerebellar-brainstem interaction in the adaptive control of the vestibuloocular reflex. Acta Otolaryngol Suppl. 1991;481: 428 – 432. 41 Zeigelboim BS, Arruda WO, MangabeiraAlbernaz PL, et al. Vestibular findings in relapsing, remitting multiple sclerosis: a study of thirty patients. Int Tinnitus J. 2008;14:139 –145. 42 Kasser SL, Rose DJ, Clark S. Balance training for adults with multiple sclerosis: multiple case studies. Neurology Report. 1999; 23:5–12. Available at: http://findarticles. com/p/articles/mi_qa3959/is_199903/ai_ n8831762/. Accessed April 2009. 43 Cattaneo D, Jonsdottir J, Zocchi M, Regola A. Effects of balance exercises on people with multiple sclerosis: a pilot study. Clin Rehabil. 2007;21:771–781. 44 Schuhfried O, Mittermaier C, Jovanovic T, et al. Effects of whole-body vibration in patients with multiple sclerosis: a pilot study. Clin Rehabil. 2005;19:834 – 842. 45 Cass SP, Borello-France D, Furman JM. Functional outcome of vestibular rehabilitation in patients with abnormal sensoryorganization testing. Am J Otol. 1996;17: 581–594. 46 Herdman SJ. Exercise strategies in vestibular disorders. Ear Nose Throat J. 1989; 68:961–964. 47 White LJ, Dressendorfer RH. Exercise and multiple sclerosis. Sports Med. 2004;34: 1077–1100. 48 Savci S, Inal-Ince D, Arikan H, et al. Sixminute walk distance as a measure of functional exercise capacity in multiple sclerosis. Disabil Rehabil. 2005;27:1365–1371. 49 ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories. ATS statement: guidelines for the sixminute walk test. Am J Respir Crit Care Med. 2002;166:111–117. 50 Cattaneo D, Regola A, Meotti M. Validity of six balance disorders scales in persons with multiple sclerosis. Disabil Rehabil. 2006;28:789 –795. 51 Beck AT, Ward CH, Mendelson M, et al. An Inventory for measuring depression. Arch Gen Psychiatry. 1961;4:561–571. 52 Kirkman, TW. Statistics to use. College of Saint Benedict and Saint John’s University. Published 1996. Available at: http://www. physics.csbsju.edu/stats. Accessed June 11, 2010. 1180 f Physical Therapy Volume 91 53 Cohen J. Statistical Power Analysis for the Behavioral Sciences. 2nd ed. Hillsdale, NJ: Lawrence Erlbaum Associates Inc; 1988. 54 LeCroy CW, Krysik J. Understanding and interpreting effect size measures. Soc Work Res. 2007;31:243–248. Available at: http://findarticles.com/p/articles/mi_ hb6481/is_4_31/ai_n29405442/?tag⫽ content;col1. Accessed April 2009. 55 University of Colorado at Colorado Springs, Psychology Department. Effect size calculators. Available at: http://www. uccs.edu/⬃faculty/lbecker/. Accessed June 11, 2010. 56 Schulz KH, Gold SM, Witte J, et al. Impact of aerobic training on immune-endocrine parameters, neurotrophic factors, quality of life and coordinative function in multiple sclerosis. J Neurol Sci. 2004;225:11– 18. 57 Wrisley DM, Stephens MJ, Mosley S, et al. Learning effects of repetitive administrations of the sensory organization test in healthy young adults. Arch Phys Med Rehabil. 2007;88:1049 –1054. 58 Badke MB, Miedaner JA, Shea TA, et al. Effects of vestibular and balance rehabilitation on sensory organization and dizziness handicap. Ann Otol Rhinol Laryngol. 2005;114(1 pt 1):48 –54. 59 Dobkin BH. Neurobiology of rehabilitation. Ann N Y Acad Sci. 2004;1038:148 – 170. 60 De Stefano N, Matthews PM, Narayanan S, et al. Axonal dysfunction and disability in a relapse of multiple sclerosis: longitudinal study of a patient. Neurology. 1997;49: 1138 –1141. 61 De Stefano N, Matthews PM, Fu L, et al. Axonal damage correlates with disability in patients with relapsing-remitting multiple sclerosis: results of a longitudinal magnetic resonance spectroscopy study. Brain. 1998;121(pt 8):1469 –1477. 62 Mark VW, Taub E, Bashir K, et al. Constraint-induced movement therapy can improve hemiparetic progressive multiple sclerosis: preliminary findings. Mult Scler. 2008;14:992–994. 63 Morgen K, Kadom N, Sawaki L, et al. Training-dependent plasticity in patients with multiple sclerosis. Brain. 2004; 127(pt 11):2506 –2517. 64 Saini S, De Stefano N, Smith S, et al. Altered cerebellar functional connectivity mediates potential adaptive plasticity in patients with multiple sclerosis. J Neurol Neurosurg Psychiatry. 2004;75:840 – 846. 65 Wegner C, Filippi M, Korteweg T, et al. Relating functional changes during hand movement to clinical parameters in patients with multiple sclerosis in a multicentre fMRI study. Eur J Neurol. 2008;15: 113–122. 66 Schor CM. Neuromuscular plasticity and rehabilitation of the ocular near response. Optom Vis Sci. 2009;86:E788 –E802. Number 8 67 Niestroy A, Rucker JC, Leigh RJ. Neuroophthalmologic aspects of multiple sclerosis: using eye movements as a clinical and experimental tool. Clin Ophthalmol. 2007;1:267–272. 68 Downey DL, Stahl JS, Bhidayasiri R, et al. Saccadic and vestibular abnormalities in multiple sclerosis: sensitive clinical signs of brainstem and cerebellar involvement. Ann N Y Acad Sci. 2002;956:438 – 440. 69 Derwenskus J, Rucker JC, Serra A, et al. Abnormal eye movements predict disability in MS: two-year follow-up. Ann N Y Acad Sci. 2005;1039:521–523. 70 Lawrence GP, Khan MA, Buckolz E, Oldham AR. The contribution of peripheral and central vision in the control of movement amplitude. Hum Mov Sci. 2006;25: 326 –338. 71 Mello RG, Oliveira LF, Nadal J. Anticipation mechanism in body sway control and effect of muscle fatigue. J Electromyogr Kinesiol. 2007;17:739 –746. 72 Filippi M, Rocca MA, Colombo B, et al. Functional magnetic resonance imaging correlates of fatigue in multiple sclerosis. Neuroimage. 2002;15:559 –567. 73 Penner IK, Bechtel N, Raselli C, et al. Fatigue in multiple sclerosis: relation to depression, physical impairment, personality and action control. Mult Scler. 2007; 13:1161–1167. 74 Mills RJ, Young CA. The relationship between fatigue and other clinical features of multiple sclerosis. Mult Scler. 2010 December 6 [Epub ahead of print]. 75 Sabapathy NM, Minahan CL, Turner GT, Broadley SA. Comparing endurance-and resistive-exercise training in people with multiple sclerosis. Clin Rehabil. 2011;25: 14 –24. 76 Kileff J, Ashburn A. A pilot study of the effect of aerobic exercise on people with moderate disability multiple sclerosis. Clin Rehabil. 2005;19:165–169. 77 Savci S, Inal-Ince D, Arikan H, et al. Sixminute walk distance as a measure of functional exercise capacity in multiple sclerosis. Disabil Rehabil. 2005;27:1365–1371. 78 Goldman MD, Marrie RA, Cohen JA. Evaluation of the six-minute walk test in multiple sclerosis subjects and healthy controls. Mult Scler. 2008;14:383–390. 79 Wuyts FL, Furman J, Vanspauwen R, Van de Heyning P. Vestibular function testing. Curr Opin Neurol. 2007;20:19 –24. August 2011 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Appendix 1. Vestibular Rehabilitation Protocol: Tasks Performed in Sequential Order 1 to 26a Upright Postural Control A. Static Body Position: Standing Eyes Open 1. BOS: firm surface— heels and toes together* 2. BOS: firm surface—partial heel to toes* 3. BOS: firm surface—full heel to toes (tandem)* Perform 1–3 with: — Ball catching and tossing (from and to investigator) — Head movement: rotate side to side* — Head movement: head up (neck extension) and down (neck flexion)* Eyes Closed 4. BOS: firm surface—shoulder width apart* 5. BOS: firm surface— heels and toes together* 6. BOS: firm surface—partial heel to toes* 7. BOS: firm surface—full heel to toes (tandem)* Eyes Open 8. BOS: foam cushion— heels and toes together* 9. BOS: foam cushion—partial heel to toes* 10. BOS: foam cushion—full heel to toes (tandem)* Perform 8 –10 with: — Ball catching and tossing (from and to investigator) — Head movement: rotate side to side* — Head movement: head up (neck extension) and down (neck flexion)* Eyes Closed 11. BOS: foam cushion—shoulder width apart* 12. BOS: foam cushion— heels and toes together* 13. BOS: foam cushion—partial heel to toes* 14. BOS: foam cushion—full heel to toes (tandem)* Eyes Open 15. BOS: tiltboard Perform 15 with: — Side-to-side Frontal plane of motion, rock tiltboard in plane of motion and stabilize tiltboard in neutral plane of motion position — Head rotated side to side Right rotation when tiltboard rocked to right, left rotation when tiltboard rocked to left — Forward and backward Sagittal plane of motion, rock tiltboard in plane of motion and stabilize tiltboard in neutral plane of motion position — Head movement: head up (neck extension) and down (neck flexion) Neck extension when tiltboard rocked backward, head flexion when rocked forward B. Static Body Position: Half-Kneeling Eyes Open 16. BOS: half-kneeling Perform 16 with: — Bilateral arm flexion (both arms lifted above head at same time)* — Alternate arm flexion/extension (one arm lifted above head, other arm moved backward), with trunk rotation* (Continued) August 2011 Volume 91 Number 8 Physical Therapy f 1181 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Appendix 1. Continued C. Static Body Position: Standing Eyes Open 17. BOS: trampoline—shoulder width apart Perform 17 with: — Head movement: rotate side to side — Head movement: head up (neck extension) and down (neck flexion) — Marching in place combined with turning body 360° right and left 18. BOS: trampoline— heels and toes together 19. BOS: trampoline—partial heel to toes 20. BOS: trampoline—full heel to toes (tandem) Perform 18 –20 with: — Head movement: rotate side to side — Head movement: head up (neck extension) and down (neck flexion) Eyes Closed 21. BOS: trampoline—shoulder width apart 22. BOS: trampoline— heels and toes together Perform 22 with: — Short squats: 5 repetitions 23. BOS: trampoline—partial heel to toes 24. BOS: trampoline—full heel to toes (tandem) D. Dynamic Body Motion: Walking 25. Walking — Heel-toe walking forward and back with and without head movements* — Walking tossing ball side to side and up and down while visually tracking ball — On-command walking with 180° change in direction, stop-start, and transition into and out of standing on one leg Eye Movement Training 26. Eye movements — Saccades Perform with: quick eye movement between 2 stationary objects in horizontal, vertical, and 2-direction diagonals* — Smooth pursuit Perform with: visually tracking a moving object in horizontal, vertical, and 2-direction diagonals* — Vestibular ocular reflex Perform with: visually fixating on immovable object while turning head side to side and up and down* a BOS⫽base of support. Asterisk indicates item included in home exercise program. 1182 f Physical Therapy Volume 91 Number 8 August 2011 Effects of Vestibular Rehabilitation on Multiple Sclerosis–Related Fatigue and Upright Postural Control Appendix 2. Submaximal Graded Exercise Test (GET) Protocola Equipment/Instruments: — Bicycle ergometer — Borg Rating of Perceived Exertion (RPE) Scale (6 –20) — Heart rate monitor — Stethoscope and blood pressure cuff Pretest measurements: — Heart rate — Borg RPE Scale rating — Blood pressure Stages: Initial stage — 2- to 3-minute warm-up — Pedal rate of 50 rpm — Workload of approximately 25 W (1 lb [0.5 kg]) — Heart rate continuously monitored — Blood pressure at end of stage Incremental stages (2 minutes each) — Pedal rate maintained at 50 rpm — Incremental workload increases of approximately 12.5 W (0.5 lb [0.25 kg]) per stage — Heart rate continuously monitored — Blood pressure recorded at the end of each stage — Borg RPE Scale rating at the end of the last minute of each stage Test termination: — Patient reports unable to continue due to exertion or fatigue symptoms, serving as the symptom-limiting endpoint for the submaximal GET — Record: Borg RPE Scale rating and peak heart rate a Protocol derived from: White LJ, Dressendorfer RH. Exercise and multiple sclerosis. Sports Med. 2004;34:1077–1100. August 2011 Volume 91 Number 8 Physical Therapy f 1183 Research Report Electromyographic Activity of the Cervical Flexor Muscles in Patients With Temporomandibular Disorders While Performing the Craniocervical Flexion Test: A Cross-Sectional Study Susan Armijo-Olivo, Rony Silvestre, Jorge Fuentes, Bruno R. da Costa, Inae C. Gadotti, Sharon Warren, Paul W. Major, Norman M.R. Thie, David J. Magee S. Armijo-Olivo, BScPT, MSc, PhD, Department of Physical Therapy, Faculty of Rehabilitation Medicine, and Alberta Research Centre for Health Evidence, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada. Mailing address: Department of Physical Therapy, Rehabilitation Research Centre, Faculty of Rehabilitation Medicine, University of Alberta, 3–50 Corbett Hall, Edmonton, Alberta, Canada T6G 2G4. Address all correspondence to Dr Armijo-Olivo at: [email protected] or [email protected]. R. Silvestre, BScPT, MSc, Research Center of Human Movement, Mayor University, Santiago, Chile. J. Fuentes, BSc, MScRS, Rehabilitation Research Centre, Faculty of Rehabilitation Medicine, University of Alberta, and Department of Physical Therapy, Catholic University of Maule, Talca, Chile. B.R. da Costa, BScPT, MSc, Institute of Social & Preventive Medicine, University of Bern, Bern, Switzerland. I.C. Gadotti, BScPT, MScPT, PhD, Department of Physical Therapy, College of Nursing and Health Sciences, Florida International University, Miami, Florida. S. Warren, PhD, Faculty of Rehabilitation Medicine, University of Alberta. Author information continues on next page. Background. Most patients with temporomandibular disorders (TMD) have been shown to have cervical spine dysfunction. However, this cervical dysfunction has been evaluated only qualitatively through a general clinical examination of the cervical spine. Purpose. The purpose of this study was to determine whether patients with TMD had increased activity of the superficial cervical muscles when performing the craniocervical flexion test (CCFT) compared with a control group of individuals who were healthy. Design. A cross-sectional study was conducted. Methods. One hundred fifty individuals participated in this study: 47 were healthy, 54 had myogenous TMD, and 49 had mixed TMD. All participants performed the CCFT. Data for electromyographic activity of the sternocleidomastoid (SCM) and anterior scalene (AS) muscles were collected during the CCFT for all participants. A 3-way mixed-design analysis of variance for repeated measures was used to evaluate the differences in EMG activity for selected muscles while performing the CCFT under 5 incremental levels. Effect size values were calculated to evaluate the clinical relevance of the results. Results. Although there were no statistically significant differences in electromyographic activity in the SCM or AS muscles during the CCFT in patients with mixed and myogenous TMD compared with the control group, those with TMD tended to have increased activity of the superficial cervical muscles. Limitations. The results obtained in this research are applicable for the group of individuals who participated in this study under the protocols used. They could potentially be applied to people with TMD having characteristics similar to those of the participants of this study. Conclusion. This information may give clinicians insight into the importance of evaluation and possible treatment of the deep neck flexors in patients with TMD. However, future research should test the effectiveness of this type of program through a randomized controlled trial in people with TMD in order to determine the real value of treating this type of impairment in this population. Post a Rapid Response to this article at: ptjournal.apta.org 1184 f Physical Therapy Volume 91 Number 8 August 2011 Cervical Flexor Activity and Temporomandibular Disorders P.W. Major, DDS, MSc, FRCD(c), School of Dentistry, University of Alberta. N.M.R. Thie, BSc, MSc, DDS, TMD/Orofacial Pain Graduate Program, School of Dentistry, University of Alberta. D.J. Magee, PhD, Department of Physical Therapy, Faculty of Rehabilitation Medicine, University of Alberta. [Armijo-Olivo S, Silvestre R, Fuentes J, et al. Electromyographic activity of the cervical flexor muscles in patients with temporomandibular disorders while performing the craniocervical flexion test: a cross-sectional study. Phys Ther. 2011;91:1184 –1197.] © 2011 American Physical Therapy Association Published Ahead of Print: June 9, 2011 Accepted: April 8, 2011 Submitted: July 14, 2010 T emporomandibular disorders (TMD) are the most prevalent category of nondental chronic pain conditions in the orofacial region. These disorders are characterized by pain affecting the masticatory muscles, the temporomandibular joint (TMJ), and related structures.1 Temporomandibular disorders interfere with daily activities and can significantly affect quality of life, diminishing patients’ capacity for work and ability to interact with their social environment.2 It has been calculated that approximately $2 billion has been spent in the United States due to TMD direct care.3 Patients with TMD have shown high levels of unemployment and decreased work effectiveness.4 In a large, population-based, crosssectional study, it was shown that TMD chronic pain had an individual impact and burden similar to that of back pain, severe headache, and chest and abdominal pain.5 In a recent study,6 women comprised more than 70% of the patients having TMD, and the ratio between women and men was 2.4:1 for arthralgia, 2.5:1 for osteoarthritis, 3.4:1 for myofascial pain, and 5.1:1 for TMJ disk displacement.6 The literature supports the fact that women are more sensitive to pain conditions, reporting more severe pain, more frequent pain, and pain of longer duration than men.7–14 In addition, women are more prompt in seeking help than men. Therefore, it seems that women more commonly have TMD and may seek care for TMD pain more often than men.3 Temporomandibular disorders have commonly been associated with symptoms affecting the head and neck region, such as headache, cervical spine dysfunction,15,16 and altered head and cervical posture.17–21 It has been reported that pain in the cervical musculoskeletal tissues may be referred to cranial August 2011 structures, including the jaw muscles22,23; thus, a connection between cervical muscle dysfunction and jaw symptoms could exist.24 –27 Additionally, animal studies have revealed considerable convergence of craniofacial and cervical afferents in the trigeminocervical nucleus and upper cervical nociceptive neurons.28 –31 All of this evidence has been the theoretical foundation of pain localization and referral and of neuromuscular adaptations in the cervical and orofacial regions.32–34 However, to date, no research has demonstrated a cause-and-effect relationship. As stated above, TMD are categorized as musculoskeletal disorders that commonly involve the cervical region. Other musculoskeletal disorders associated with the cervical region, such as neck pain, cervicogenic headache, and whiplashassociated disorders, are characterized by abnormal function of the cervical muscles.35–37 However, it is unknown whether people with TMD have these muscular alterations. Given the close connection between the cervical spine and the orofacial region, knowledge about impairments in the cervical spine in people with TMD could help clinicians focus their efforts on properly evaluating and treating these impairments. Previous work has shown that gross changes in strength (force-generating capacity) and endurance have been observed in cervical-related disorders. However, according to Jull et al36 and Falla and Farina,38 finer changes in cervical muscular activity of the cervical spine are present. Reduced activation of deep cervical muscles, augmented superficial activity of the sternocleidomastoid (SCM) and anterior scalene (AS) muscles, changes in feedforward activation, reduced capacity to relax the cervical muscles, and prolonged muscle activity following voluntary contraction could lead to a compromise in Volume 91 Number 8 Physical Therapy f 1185 Cervical Flexor Activity and Temporomandibular Disorders the control of the cervical spine and consequently lead to pain and dysfunction.36 Study of these muscular alterations has gained attention in the last few years, as exercises addressing these motor control alterations have had good results in patients with cervical involvement.39 – 41 Therefore, the assessment and treatment of muscular impairments is considered a key element in the management of cervicalassociated disorders. Because TMD have been considered part of the cervical-associated disorders, it may be plausible that similar features could be seen in this patient group. Knowledge about these features would be useful for clinicians treating patients with TMD. However, studies of muscular impairments in patients with TMD are lacking. Cervical dysfunction in patients with TMDs has been evaluated only qualitatively through a general clinical examination of the cervical spine. Most of the studies have looked at cervical spine signs and symptoms in people with TMD, but they have not investigated any motor alterations in a quantitative way. For example, de Wijer and colleagues27,42 concluded that symptoms of the stomatognathic system overlap in patients with TMD and cervical spine disorders and that symptoms of the cervical spine overlap in the same group of patients. Visscher et al25 found that patients with chronic TMD more often had cervical spine pain than those without this disorder. Stiesch-Scholz et al43 found that asymptomatic functional disorders of the cervical spine occurred more frequently in patients with internal derangement of the TMJ than in a control group. The presence of tender points in the cervical spine and shoulder girdle in patients with the same diagnosis was more common, especially in upper segments of the The Bottom Line What do we already know about this topic? Cervical spine dysfunction has been reported to be associated with temporomandibular disorders (TMD). Temporomandibular disorders also are commonly associated with other symptoms affecting the head and neck region such as headache, ear-related symptoms, and altered head and cervical posture. However, no study has investigated the presence of cervical muscle impairments using electromyography. What new information does this study offer? The results of this study may give clinicians insight into the importance of the evaluation and possible treatment of the deep neck flexors in patients with TMD. However, randomized clinical trials are necessary to determine the effectiveness of an exercise program targeting the deep neck flexors in these patients. If you’re a patient, what might these findings mean for you? If you have a TMD, these findings may help your physical therapist evaluate your condition. This evaluation would include an examination of the cervical musculature as well as the TMD. 1186 f Physical Therapy Volume 91 Number 8 cervical spine, compared with a control group of individuals who were healthy. Furthermore, a recent systematic review44 showed that exercises for the neck that also were used to improve neck and head posture decreased symptoms in patients with TMD. However, the systematic review found that details of the exercises and exercise programs (ie, type of exercise, dosage, and frequency) were lacking, as well as a clear underlying mechanism of why these exercises, directed toward to the neck, improved TMD symptoms. Based on the above information, it was evident that a more quantitative evaluation of the motor activity of the cervical muscles through electromyographic (EMG) assessment, looking at performance patterns of the cervical musculature activity in patients with TMD, could assist in clarifying the role of the cervical muscles’ involvement in the symptoms of these patients. Additionally, this evaluation could open an area of study aimed at treating these alterations through improvement of motor control of the cervical muscles in patients with TMD. The main objective of this study was to determine, through EMG evaluation, whether patients with myogenous TMD and mixed TMD had altered muscle activity (ie, higher EMG activity) of the superficial cervical muscles (SCM and AS) when performing the CCFT compared with a control group of individuals who were healthy. The secondary objectives of this study were: (1) to determine whether there was an association between the performance of the cervical flexor muscles during the 5 stages of the CCFT and neck disability and jaw disability and (2) to determine whether there was an association between level of chronic disability in patients with TMD based on the Research Diagnostic Criteria for Temporomandibular August 2011 Cervical Flexor Activity and Temporomandibular Disorders Disorders45 (RDC/TMD) (Chronic Pain Grade Disability Questionnaire for TMD), pain intensity, duration of complaint, and performance of the cervical flexor muscles during the 5 stages of the CCFT. Table 1. Descriptive Statistics of Height, Weight, and Age and Clinical Characteristics of Participants by Groupa Variable Height (cm) Method Design A cross-sectional conducted. Weight (kg) study was Age (y) Participants A convenience sample of patients who attended the TMD/Orofacial Pain Clinic at the School of Dentistry, Faculty of Medicine and Dentistry, University of Alberta, and students and staff at the University of Alberta who were healthy was recruited for this study. The sample size for this study was calculated based on a repeated-measures analysis of variance (ANOVA) following the guidelines established by Stevens (with ␣⫽.05, ⫽0.20, power⫽80%, and effect size⫽0.57).46 A minimum of 40 participants per group was needed. The inclusion and exclusion criteria for the individuals who were healthy and the patients with TMD have been described elsewhere.47,48 In brief, people who were healthy were included if they were women between the ages of 18 and 50 years16 and they did not have a history of musculoskeletal pain, TMD symptoms, neurological disease, systemic disease, or mental illness that could interfere with the outcomes. Patients with TMD were included if they were women between 18 and 50 years of age, had pain in the masticatory muscles or TMJ of at least 3 months’ duration, and had a moderate or severe baseline pain score (ⱖ30 mm) on a 100-mm visual analog scale (VAS).49 Patients were classified as having myogenous TMD based on the classification Ia and Ib of Dworkin and LeResche.45 In addition, they had to have pain upon palpation in at least 3 of the 12 musAugust 2011 Duration of complaint (y) Pain intensity (0–100 mm) Group Jaw Function Scale (10–50 points) a b c SD 165.1 5.1 Healthy (n⫽47) 165.0 6.8 Mixed TMD (n⫽49) 166.3 5.9 Myogenous TMD 64.1 b 9.9 Healthy 64.3b 12.7 Mixed TMD 72.1c 15.9 Myogenous TMD 31.4 9.0 Healthy 28.3 7.5 Mixed TMD 31.3 8.3 Myogenous TMD 6.5c 6.4 Healthy 0.0 0.0 Mixed TMD 8.3c 6.4 45.3c 17.3 Myogenous TMD Healthy Neck Disability Index (0–50 points) X Myogenous TMD (n⫽54) 0.0 0.0 Mixed TMD 49.0c 16.1 Myogenous TMD 10.5c 5.5 1.6 1.6 Mixed TMD 12.6c 6.8 Myogenous TMD 18.6b,c 6.6 Healthy 10.1 0.4 Mixed TMD 22.7c 7.1 Healthy TMD⫽temporomandibular disorders. Significantly different compared with participants with mixed TMD at ␣⫽.05. Significantly different compared with participants who were healthy at ␣⫽.05. cular points proposed by Fricton and Schiffman.50 –52 Patients were diagnosed as having mixed TMD if they complained of muscular symptoms in addition to TMJ symptoms such as painful clicking, crepitation, or pain in the TMJ at rest or during function53 and during a compression test.54 A total 168 individuals were assessed for inclusion in this study. A total of 18 individuals were excluded. The main reasons for exclusion were: not totally healthy (n⫽9), older than 50 years of age (n⫽2), having a neurological disease (n⫽1), having cancer (n⫽1), and having a pain score lower than 30 mm on the VAS (n⫽5). One hundred fifty participants provided data for this study: 47 were healthy, 54 had myogenous TMD, and 49 had mixed TMD. The general demographics for each group and the clinical characteristics of the participants are displayed in Table 1. There were no significant differences in age and height in the sample (P⬎.05). However, weight was significantly different between participants with mixed TMD and those with myogenous TMD (mean difference⫽8.0 kg, 95% confidence interval [CI]⫽1.9 to 14.2; P⫽.006) and between participants with mixed TMD and those who were healthy (mean difference⫽7.8 kg, 95% CI⫽1.4 to 14.2; P⫽.01). Participants with mixed TMD were similar to those with myogenous Volume 91 Number 8 Physical Therapy f 1187 Cervical Flexor Activity and Temporomandibular Disorders TMD in most of the general characteristics such as duration of complaint and pain intensity (P⬎.05). Both groups had a moderate intensity of pain in the jaw and a long history of pain. Both groups also had a mild level of disability in the neck and a moderate level of disability in the jaw (Tab. 1). The Limitations of Daily Functions in TMD Questionnaire/Jaw Function Scale (JFS) disability score was significantly higher for participants with mixed TMD compared with those with myogenous TMD (mean difference⫽4.1 points, 95% CI⫽1.4 to 6.9; P⫽.001). The prevalence of neck pain in the sample of participants with TMD was high. Approximately 88% (87.5%) of the participants with myogenous TMD and 87.8% of those with mixed TMD had self-reported neck pain. Clinical Examination The participants underwent a clinical examination by a physical therapist with experience in musculoskeletal rehabilitation to determine eligibility for this study and to determine their diagnosis. The clinical examination followed the guidelines of the RDC/TMD.45 All participants read an informational letter and signed an informed consent statement in accordance with the University of Alberta’s policies on research using human subjects. Procedure Demographic data were collected on all participants who satisfied the inclusion criteria. In addition, all included participants were asked to report specific characteristics regarding their jaw problem (eg, onset, duration of symptoms, treatments received) and their intensity of pain in the jaw (VAS score)49,55–58 and to complete the Neck Disability Index (NDI),59,60 the JFS,61 and a questionnaire for history of jaw pain used by the RDC/TMD.45 In addition, participants were asked to complete 1188 f Physical Therapy Volume 91 the Chronic Pain Grade Disability Questionnaire for TMD used by the RDC/TMD to evaluate the level of chronic disability due to TMDs.45 The reliability and validity of these tools have been reported elsewhere.45,59 – 61 After the participants were evaluated clinically and had completed the questionnaires, they performed the CCFT. This testing was performed in one session. Electromyographic Evaluation of the Cervical Flexor Muscles Electrode placement. Surface electrodes were located on the sternal head of the SCM muscle and on the AS muscle as described in the protocol used by Falla and colleagues.62,63 A reference electrode was placed on the wrist. Normalization procedure for EMG data. For normalization purposes, EMG data were collected for 5 seconds during a maximal voluntary contraction (MVC). The EMG activity of the SCM and AS muscles was recorded during this maximal contraction and saved in the computer. This procedure was repeated a second time. Submaximal contractions obtained during the CCFT were normalized using these 2 MVC values. Submaximal contractions were expressed as a percentage of the 3-second root mean square (RMS) value obtained during the MVC. The average between the normalized contractions using the 2 MVC measurements was used for statistical analysis. EMG data processing. Data on EMG activity of the SCM and AS muscles were obtained using the Bagnoli-8 EMG system* in a bipolar configuration with DE-2.1 electrodes.* This system is designed to make the acquisition of EMG signals easy and reliable (common-mode rejection ratio⫽92 dB, system * Delsys Inc, PO Box 15734, Boston, MA 02215. Number 8 noise⬍1.2 V [RMS]). The EMG activity was recorded (analog raw signal) with a data acquisition program, written in Labview 7.1,† which collected data at 1,024 Hz using a PCMCIA card† filtered between 20 and 450/Hz ⫾10% and amplified using a gain of 1,000 according to the established standards for EMG acquisition and reporting.64,65 To obtain a measure of EMG amplitude, maximum root mean square (RMS) was calculated for 4 seconds during the 10-second submaximal contractions for each muscle while performing the CCFT using IGOR Pro5.1‡ and was expressed a percentage of the 3-second EMG activity obtained during the MVC normalization procedure. Instrumentation for Registering the Pressure Exerted While Performing the CCFT An air-filled pressure sensor (pressure biofeedback unit) was placed in the suboccipital region of each patient’s neck and inflated to a pressure of 20 mm Hg. The cuff was connected to a pressure transducer (miniature pressure cell) designed to register increases in pressure with the movement of nodding action for the CCFT. Electrical signals from the pressure transducer were amplified to a visual feedback device and projected onto a computer screen so that the participants were able to see the targeted pressure level. Graphs with the performance of each participant during the CCFT were stored using Igor Pro5.1. These data were analyzed offline by a blinded assessor. Craniocervical Flexion Test: Description and Procedures Before testing began, participants were asked to perform a warm-up, which consisted of 2 movements of the neck and head in all directions † National Instruments Corporation, 11500 N Mopac Expwy, Austin, TX 78759-3504. ‡ WaveMetrics Inc, PO Box 2088, Lake Oswego, OR 97035. August 2011 Cervical Flexor Activity and Temporomandibular Disorders (flexion [forward neck movement], extension, side flexion [lateral movement of the neck], and rotation). The participants were placed in a relaxed supine position with the knees flexed and the head and neck maintained in a mid-position (ie, neutral position, no flexion or extension) following a protocol established previously.66 The head and chin were parallel to the plinth (Fig. 1). The CCFT is a low-load test that is the most common method used to evaluate the performance of the deep cervical muscles (ie, longus colli and rectus capitis). The CCFT consists of a craniocervical flexion (nodding) movement, which combines the action of flexion at the craniocervical junction, performed by the longus capitis muscles, along with the flattening of the cervical lordosis, an action of the longus colli muscles. Electromyographic activity of the superficial cervical flexor muscles such as the SCM and AS may be registered during the CCFT. Elevated EMG activity may be a compensation for reduced or impaired activity of the deep cervical flexor muscles in individuals with cervical-associated pain compared with those who are healthy.67 The CCFT required each participant to perform the craniocervical flexion movement in 5 progressive stages of increasing pressure (22, 24, 26, 28, and 30 mm Hg) with the aid of a visual feedback device. Participants were instructed to perform this gentle nodding movement (craniocervical flexion) and at practiced progressive targeted pressure levels. The order of the targeted pressure level was randomized by an independent assessor. Participants had to maintain a steady pressure at each targeted level for a duration of 10 seconds (Fig. 1). They repeated each targeted level 2 times, with a rest period of 1 minute between repetitions to avoid the effects of fatigue.68 August 2011 Figure 1. Craniocervical flexion test. Data Analysis The normalized data of the EMG activity of all muscles were analyzed descriptively (ie, mean, standard deviation). Variables were tested for normality, homogeneity of variance, and linearity. All EMG variables were reasonably normally distributed. Histograms and box plots show that most of the variables were slightly skewed to the right. However, ANOVA analysis is robust to these mild deviations from normality and can provide accurate estimates of the analyzed variables.69 A 3-way mixed-design ANOVA for repeated measures (3 independent variables: muscles [SCM and AS], test [5 levels], and groups [myogenous TMD, mixed TMD, and control]) was used to evaluate the differences in EMG activity for selected muscles (dependent variable) while performing the CCFT at 5 levels of pressure. Pair-wise comparisons using the Bonferroni procedure were administered to evaluate the differences between variables and groups (ie, control and TMD groups) in all of the different conditions (objective 1). The Spearman rho test was used to evaluate the relationship among NDI, JFS, and clinical variables with EMG variables (correlational matrix) (objectives 2 and 3). The correlation was considered important when the correlation coefficient value was higher than .70. The reference values to make this decision were based on values reported by Munro.70 To clearly show the impact of the results for clinical practice, clinical relevance of the results was assessed using a distribution-based method.71 The effect size (Cohen d) values were calculated to determine clinical relevance of the differences in the EMG measurements across different Volume 91 Number 8 Physical Therapy f 1189 Cervical Flexor Activity and Temporomandibular Disorders Myogenous TMD Healthy Mixed TMD Normalized EMG Activity (%MVC) 60 50 40 30 20 10 AvASL_30mmHg AvASR_30mmHg AvSCML_30mmHg AvSCMR_30mmHg AvASL_28mmHg AvASR_28mmHg AvSCML_28mmHg AvSCMR_28mmHg AvASL_26mmHg AvASR_26mmHg AvSCML_26mmHg AvSCMR_26mmHg AvASL_24mmHg AvASR_24mmHg AvSCML_24mmHg AvSCMR_24mmHg AvASL_22mmHg AvASR_22mmHg AvSCML_22mmHg AvSCMR_22mmHg AvASL_30mmHg AvASR_30mmHg AvSCML_30mmHg AvSCMR_30mmHg AvASL_28mmHg AvASR_28mmHg AvSCML_28mmHg AvSCMR_28mmHg AvASL_26mmHg AvASR_26mmHg AvSCML_26mmHg AvSCMR_26mmHg AvASL_24mmHg AvASR_24mmHg AvSCML_24mmHg AvSCMR_24mmHg AvASL_22mmHg AvASR_22mmHg AvSCML_22mmHg AvSCMR_22mmHg AvASL_30mmHg AvASR_30mmHg AvSCML_30mmHg AvSCMR_30mmHg AvASL_28mmHg AvASR_28mmHg AvSCML_28mmHg AvSCMR_28mmHg AvASL_26mmHg AvASR_26mmHg AvSCML_26mmHg AvSCMR_26mmHg AvASL_24mmHg AvASR_24mmHg AvSCML_24mmHg AvSCMR_24mmHg AvASL_22mmHg AvASR_22mmHg AvSCML_22mmHg AvSCMR_22mmHg 0 Figure 2. Normalized electromyographic (EMG) activity of sternocleidomastoid (SCM) and anterior scalene (AS) muscles in participants with myogenous temporomandibular disorders (TMD), those with mixed TMD, and those who were healthy while performing the craniocervical flexion test. Error bars⫽95% confidence interval. %MVC⫽percentage of maximum voluntary contraction, AvSCMR_22mmHg⫽average right SCM muscle EMG activity at 22 mm Hg, AvSCML_22mmHg⫽average left SCM muscle EMG activity at 22 mm Hg, AvASR_22mmHG⫽average right AS muscle EMG activity at 22 mm Hg, AvASL_22mmHg⫽average left AS muscle EMG activity at 22 mm Hg, AvSCMR_24mmHg⫽average right SCM muscle EMG activity at 24 mm Hg, AvSCML_24mmHg⫽average left SCM muscle EMG activity at 24 mm Hg, AvASR_24mmHg⫽average right AS muscle EMG activity at 24 mm Hg, AvASL_24mmHg⫽average left AS muscle EMG activity at 24 mm Hg, AvSCMR_26mmHg⫽average right SCM muscle EMG activity at 26 mm Hg, AvSCML_26mmHg⫽average left SCM muscle EMG activity at 26 mm Hg, AvASR_26mmHg⫽average right AS muscle EMG activity at 26 mm Hg, AvASL_26mmHg⫽average left AS muscle EMG activity at 26 mm Hg, AvSCMR_28mmHg⫽average right SCM muscle EMG activity at 28 mm Hg, AvSCML_28mmHg⫽average left SCM muscle EMG activity at 28 mm Hg, AvASR_28mmHg⫽average right AS muscle EMG activity at 28 mm Hg, AvASL_28mmHg⫽average left AS muscle EMG activity at 28 mm Hg, AvSCMR_30mmHg⫽average right SCM muscle EMG activity at 30 mm Hg, AvSCML_30mmHg⫽average left SCM muscle EMG activity at 30 mm Hg, AvASR_30mmHg⫽average right AS muscle EMG activity at 30 mm Hg, AvASL_30mmHg⫽average left AS muscle EMG activity at 30 mm Hg. levels of pressure and groups.72 Effect sizes of 0.4 or higher were considered clinically relevant.73 A subgroup analysis also was conducted to determine differences between participants with pure TMD (ie, without neck pain) and those who were healthy. The level of significance was set at ␣⫽.05. The SPSS version 17§ and STATA version 10㛳 statistical programs were used to perform the statistical analysis. The analysis was performed blinded to group condition. § SPSS Inc, 233 S Wacker Dr, Chicago, IL 60606. StataCorp LP, 4905 Lakeway Dr, College Station, TX 77845. 㛳 1190 f Physical Therapy Volume 91 Results EMG Activity of the Cervical Flexors Muscles While Performing the CCFT Large variability of the normalized EMG activity across conditions and groups was observed (Fig. 2). Using a 3-way mixed-design ANOVA for repeated measures, we found that the main effects of muscles (F⫽18.5, P⫽.0001) and pressure levels (F⫽27.3, P⫽.0001) were statistically significant. This finding means that there was a statistically significant difference in EMG activity among muscles and among pressure levels. The interaction between muscles and pressure also was statistically significant (F⫽2.9, P⫽.001). Number 8 However, there was no significant difference in EMG activity of the analyzed muscles among groups (ie, mixed TMD, myogenous TMD, and control) across conditions (F⫽2.6, P⫽.07). Weight was not significantly associated with EMG activity (P⫽.49), so it was not included in the model. Subgroup Analysis: EMG Activity in Patients With Pure TMD (Without Neck Pain) Compared With Participants Who Were Healthy When analyzing a subgroup of participants with TMD but without neck pain (n⫽13) compared with the control group (n⫽47), statistically significant differences in EMG August 2011 Cervical Flexor Activity and Temporomandibular Disorders Table 2. Subgroup Analysis Between Participants With Pure Temporomandibular Disorders and Participants Who Were Healthy: Electromyographic Activity of the Analyzed Muscles While Performing the Craniocervical Flexion Testa Muscle Pressure (mm Hg) Group SCMR 22 Myogenous TMD Healthy 24 Myogenous TMD SCML 95% Confidence Interval for Difference Mean Difference Between Groups (%MVC) Lower Bound Upper Bound Standard Error Pb 9.51c 3.315 .017 1.35 17.68 Healthy 11.06c 3.719 .013 1.90 20.22 c Group 28 Myogenous TMD Healthy 11.92 4.580 .035 0.637 23.20 30 Myogenous TMD Healthy 12.17c 5.149 .050 0.051 24.86 Myogenous TMD ⫺6.80 c 2.715 .045 ⫺13.48 ⫺0.11 Mixed TMD ⫺9.54c 3.380 .019 ⫺17.87 ⫺1.22 Myogenous TMD ⫺7.32 c 2.922 .045 ⫺14.52 ⫺0.124 Mixed TMD ⫺12.64c 3.637 .003 ⫺21.59 ⫺3.68 ⫺10.68 4.393 .050 ⫺21.50 9.74 3.981 .050 0.062 6.631 .033 ⫺33.759 22 24 Healthy Healthy 26 Healthy Mixed TMD ASR 22 Myogenous TMD Healthy ASL 24 Healthy Mixed TMD ⫺17.43c 0.014 19.55 ⫺1.093 a Values based on estimated marginal means. TMD⫽temporomandibular disorders, SCMR⫽right sternocleidomastoid, SCML⫽left sternocleidomastoid, ASR⫽right anterior scalene, and ASL⫽left anterior scalene. b Bonferroni adjustment for multiple comparisons. c The mean difference is significant at the .05 level. activity were found between groups (F⫽4.831, P⫽.01). Post hoc analysis using a Bonferroni test indicated there were many statistically significant differences between groups in the analyzed muscles and conditions (Tab. 2). Association Between EMG Variables and Clinical Variables While Performing the CCFT Very weak (although statistically significant) correlations were found, mainly between the EMG activity of the SCM muscles during the 5 stages of the CCFT and clinical variables such as pain intensity, duration of complaint, neck disability, jaw disability, and level of chronic disability of TMD based on the RDC/TMD (Chronic Pain Grade Disability Questionnaire for TMDs) (Tab. 3). Table 3. Correlations Between Electromyographic Activity and Neck Disability (as Measured by Neck Disability Index), Chronic Pain Grade Classification, Jaw Disability (as Measured by Jaw Function Scale), Pain Intensity, and Duration of Complainta Electromyographic Activity Neck Disability Chronic Pain Grade Classification Jaw Disability Pain Intensity Duration of Complaint (y) Average SCM at 22 mm Hg .23b .26b .26b .32b .15 b .05 Average AS at 22 mm Hg .13 .15 .15 .21 Average SCM at 24 mm Hg .23b .26b .30b .32b .19c Average AS at 24 mm Hg .14 .16 .17c .21c .08 b .29b .09 b .04 Average SCM at 26 mm Hg .18 c .19 c .24 Average AS at 26 mm Hg .13 .12 .15 .21 Average SCM at 28 mm Hg .18c .17 .23b .27b .13 c b .03 Average AS at 28 mm Hg .13 .10 .17 Average SCM at 30 mm Hg .24b .21c .28b .22 .33b .16c Average AS at 30 mm Hg .20c .18c .22b .28b .11 a SCM⫽sternocleidomastoid muscle, AS⫽anterior scalene muscle. b Correlation is significant at the .05 level. c Correlation is significant at the .01 level. August 2011 Volume 91 Number 8 Physical Therapy f 1191 Cervical Flexor Activity and Temporomandibular Disorders Table 4. Moderate Effect Sizes for Comparisons Among Groups at Different Levels of Pressure While Performing the Craniocervical Flexion Testa Raw Differences Standardized Effect Size Mean Difference (%MVC) Lower Bound Upper Bound Effect Size Lower Bound Upper Bound Effect Size Based on Healthy Group Standard Deviation Average SCMR at 22 mm Hg, mixed TMD vs healthy 5.36 1.65 9.07 0.59 0.17 0.99 0.73 Average SCMR at 24 mm Hg, mixed TMD vs healthy 5.88 1.83 9.93 0.59 0.18 0.99 0.72 Average SCMR at 28 mm Hg, mixed TMD vs healthy 5.94 0.77 11.11 0.47 0.06 0.87 0.54 Average SCMR at 30 mm Hg, mixed TMD vs healthy 6.31 0.67 11.95 0.45 0.04 0.85 0.48 Average SCML at 22 mm Hg, myogenous TMD vs healthy 5.10 0.66 9.54 0.45 0.06 0.85 0.72 Average SCML at 22 mm Hg, mixed TMD vs healthy 5.79 2.06 9.52 0.63 0.21 1.03 0.82 Average SCML at 24 mm Hg, myogenous TMD vs healthy 4.87 0.79 8.95 0.47 0.07 0.87 0.66 Average SCML at 24 mm Hg, mixed TMD vs healthy 6.53 2.49 10.57 0.66 0.24 1.06 0.89 Average SCML at 26 mm Hg, mixed TMD vs healthy 4.63 0.25 9.01 0.43 0.02 0.83 0.50 Average SCML at 30 mm Hg, mixed TMD vs healthy 5.19 0.06 10.32 0.41 0.00 0.81 0.42 Average ASR at 22 mm Hg, myogenous TMD vs healthy 6.39 0.49 12.29 0.43 0.03 0.82 0.60 Average ASR at 30 mm Hg, myogenous TMD vs healthy 12.07 1.02 23.12 0.43 0.03 0.82 0.72 8.24 0.17 16.31 0.41 0.01 0.81 0.49 Confidence Interval for Difference Outcome Measure: Electromyographic Activity Average ASR at 30 mm Hg, mixed TMD vs healthy Confidence Interval for Effect Size a TMD⫽temporomandibular disorders, SCMR⫽right sternocleidomastoid muscle, SCML⫽left sternocleidomastoid muscle, ASR⫽right anterior scalene muscle, %MVC⫽percentage of maximum voluntary contraction. Clinical Relevance Effect sizes of comparisons between mixed TMD and myogenous TMD groups compared with the control group while performing the CCFT are displayed in Table 4 and Figures 3 and 4. Discussion The main finding of this study was that, although statistically significant differences in EMG activity of the SCM and AS muscles in patients with TMD compared with participants who were healthy while performing the CCFT were not attained (P⫽.07), there was a trend for patients with 1192 f Physical Therapy Volume 91 TMD to have consistently higher EMG activity in all of the analyzed muscles. This increased activity of the superficial muscles of the cervical spine might be associated with the neck disturbances seen in patients with TMD. This information may give clinicians insight into the importance of evaluation and possible treatment of the deep neck flexors in patients with TMD. However, at this point, more research on these issues is necessary to provide definite conclusions. The results of this study cannot be directly compared with those of Number 8 other studies of cervical flexor muscle performance in patients with TMD because no studies investigating this issue in this population were found. However, the CCFT has widely been used by physical therapists to determine alterations in the motor control of the craniocervical flexor muscles in people with cervical disorders such as neck pain, whiplash-associated disorders, and cervicogenic headache because impairment of the deep flexor muscles appears to be generic to neck disorders.37 All of the studies analyzing craniocervical performance using the CCFT36,63,74,75 converge in that August 2011 Cervical Flexor Activity and Temporomandibular Disorders Study or Subgroup Mixed TMD Healthy Mean Difference IV, Fixed, 95% CI IV, Fixed, 95% CI X SD X SD ASR at 30 mm Hg 38.09 22.55 49 29.85 16.7 SCML at 22 mm Hg 22.83 10.83 49 17.04 SCML at 24 mm Hg 24.85 11.93 49 18.32 SCML at 26 mm Hg 26.61 12.07 49 21.98 SCML at 28 mm Hg 28.82 12.5 49 24.2 10.4 SCML at 30 mm Hg 30.49 12.93 49 25.3 12.35 47 7.7% 5.19 (0.13, 10.25) SCMR at 22 mm Hg 21.01 10.59 49 15.65 7.34 47 15.0% 5.36 (1.73, 8.99) SCMR at 24 mm Hg 23.19 11.48 49 17.31 8.15 47 12.5% 5.88 (1.91, 9.85) SCMR at 28 mm Hg 28.57 14.25 49 22.63 10.98 47 7.7% 5.94 (0.86, 11.02) SCMR at 30 mm Hg 30.58 14.5 49 24.2 13.27 Total (95% CI) Total Total Weight Mean Difference 47 3.2% 8.24 (0.32, 16.16) 7.09 47 14.8% 5.79 (2.14, 9.44) 7.36 47 12.7% 6.53 (2.58, 10.48) 9.29 47 10.7% 4.63 (0.33, 8.93) 47 9.4% 4.62 (0.03, 9.21) 490 47 6.4% 6.38 (0.82, 11.94) 470 100.0% 5.68 (4.27, 7.08) Heterogeneity: 2⫽1.16, df⫽9 (P⫽1.00), I2⫽0% Test for overall effect: Z⫽7.92 (P⬍.00001) Figure 3. Moderate effect sizes found for comparisons between participants with mixed temporomandibular disorders (TMD) and those who were healthy at different levels of pressure while performing the craniocervical flexion test. IV⫽inverse variance, 95% CI⫽95% confidence interval, ASR⫽right anterior scalene muscle, SCML⫽left sternocleidomastoid muscle, SCMR⫽right sternocleidomastoid muscle. patients with cervical involvement have an impaired performance of the deep and superficial flexor cervical muscles. The increased activity in the superficial muscles could be seen as a strategy to compensate for the dysfunction of the deep flexor muscles. Sterling et al76 suggested that the presence of pain could lead to inhibition or delayed activation of Study or Subgroup specific muscles or group of muscles in the spine. This inhibition generally occurs in deep muscles such as the longus colli and longus capitis, which control joint stability.76 The results of this study are not in total agreement with those of the majority of the above-mentioned studies. In our study, we found no Myogenous TMD X SD Total Healthy X SD Total Weight statistically significant differences in superficial cervical flexor muscular activity among groups while performing the CCFT, as evaluated though EMG analysis. One possible explanation for these results could be the level of dysfunction presented by the participants with TMD. We found that the level of dysfunction, not only at the level of the neck but Mean Difference Mean Difference IV, Fixed, 95% CI IV, Fixed, 95% CI ASR at 22 mm Hg 26.05 17.83 54 19.66 10.59 47 19.3% 6.39 (0.75, 12.03) ASR at 30 mm Hg 41.92 34.82 54 29.85 16.73 47 5.6% 12.07 (1.62, 22.52) SCML at 22 mm Hg 22.14 13.83 54 17.04 7.09 47 34.7% 5.10 (0.89, 9.31) SCML at 24 mm Hg 23.19 12.3 54 18.32 7.36 47 40.4% 4.87 (0.97, 8.77) 188 100.0% Total (95% CI) 216 5.65 (3.17, 8.13) Heterogeneity: 2⫽1.74, df⫽3 (P⫽.63), I2⫽0% Test for overall effect: Z⫽4.47 (P⬍.00001) Figure 4. Moderate effect sizes found for comparisons between participants with myogenous temporomandibular disorders (TMD) and those who were healthy at different levels of pressure while performing the craniocervical flexion test. IV⫽inverse variance, 95% CI⫽95% confidence interval, ASR⫽right anterior scalene muscle, SCML⫽left sternocleidomastoid muscle. August 2011 Volume 91 Number 8 Physical Therapy f 1193 Cervical Flexor Activity and Temporomandibular Disorders also at the level of the jaw, was considered mild for our participants with TMD. We might speculate that because the disability was mild, it did not have an impact on function or physical impairment, which generally is found in people with more disabling pain. Our results are in agreement with the results obtained by Falla et al63 in individuals with a level of disability similar to that of the participants in this present study (mean NDI score⫽12.4 points, SD⫽9.563). Falla et al63 found that even though the normalized EMG amplitude of the deep cervical flexor muscles was significantly lower in patients with neck pain compared with individuals who were healthy (P⬍.05), the increase in EMG activity of the superficial muscles did not reach statistical significance, although there was a trend of increased EMG activity for the superficial muscles in patients with neck pain. The main explanation of this finding was the large variability in the EMG activity found across groups and conditions. These results agree with our findings, which also showed a large amount of variability in EMG activity among muscles and conditions (as evidenced by the wide CIs). When interpreting CIs, lower and upper boundaries need to be taken into account to make conclusions.77 Based on this interpretation, we can say that 95% of the time the estimated difference between groups could fall between these lower and upper boundaries. If we look at the upper boundaries of the CIs for the raw mean differences (Tab. 4), we can see that the difference between groups can be as high as 8.95% to 23.12% of MVC. However, if we look at the lower boundaries, the difference between groups can be as low as 0.06% to 2.49% of MVC. Therefore, based on this large variability, we could have a situation where a clinically significant difference between groups as well as a 1194 f Physical Therapy Volume 91 nonclinically significant difference between groups could occur. Although there was great variability in EMG activity, the mean EMG activity of the superficial muscles was always higher for participants with TMD pain compared with the control group across all conditions and muscles (Fig. 2). However, the large variability of the normalized EMG activity across participants and groups did not lead to a finding of statistical significance. The large variability seen in the EMG activity of the cervical flexor muscles also has been observed in other regions such as the low back.78 Hodges et al78 found that people responded differently to experimental pain in the low back muscles. They reported that no 2 individuals showed identical patterns of increased activity of the low back muscles when they underwent experimental pain. If this phenomenon were extrapolated to the cervical spine, it could be speculated that each individual has a different muscle activation strategy to adapt to pain. The motor response in the cervical spine, especially in people with pain, would be an increase of the activity of the SCM and AS muscles; however other strategies, using different muscles not investigated in this research, also could be present. Further research investigating possible cervical motor strategies in people with TMD under different conditions would help further clarify the role of the cervical muscles in TMD. Our study did not measure directly the activity of the deep cervical flexor muscles because the technique for measuring the activity of the deep cervical muscles is invasive and adherence to the testing protocol would have been impaired. We measured the superficial cervical muscles such as the SCM and AS only as an indirect measure of impairment Number 8 of the activity of the deep cervical flexor muscles. Thus, it is still uncertain whether deep cervical muscle activity was impaired in these patients. In addition, because the cervical spine is a very complex system characterized by a high degree of redundancy in the muscular system,36,79 it is not surprising that other motor strategies and muscles not analyzed in this study (other than SCM and AS muscles) could be used by people with pain to stabilize the cervical spine. The CCFT has become a gold standard for isolating the activation of the deep flexor muscles and identifying possible co-contraction patterns of superficial muscles in the cervical spine.63,75,80 Its construct validity66,81 as well as its reliability67 have been established; however, other psychometric properties such as concurrent validity with clinical variables such as neck disability and pain intensity of this test need to be ascertained. Thus, this study investigated the associations between the muscular activity of the analyzed muscles through the 5 stages of the CCFT and clinical variables such as the level of chronic pain grade classification of TMD based on the RDC/TMD, pain intensity, time of complaint, jaw disability, and neck disability. Most of the associations were positive but weak, indicating that the performance of the CCFT is not strongly related to other clinical variables such as pain intensity, neck disability, or jaw disability. These results are in agreement with those of Falla et al,82 who reported that reduction in pain in patients with neck pain after a training program was not accompanied by an improvement in performance of the cervical flexor muscles. It appears that pain and physical performance of the craniocervical muscles represent different aspects of disability in people with cervical involvement.83 Thus, a more focused evaluation August 2011 Cervical Flexor Activity and Temporomandibular Disorders regarding disability and its related factors in future research is needed to understand the intricacies among physical impairments, pain, and disability. Because of the variability of EMG activity among groups and conditions found in this study, an analysis of the clinical relevance of the results through the calculation of effect sizes was conducted to evaluate the relevance of these findings. To our knowledge, this is the first time that a study has evaluated the clinical relevance of EMG activity. According to Musselman,71 effect size calculation is one of the most common ways to evaluate clinical relevance after the fact.71,84 The larger this effect size index, the larger the difference between groups and the larger the clinical relevance of the results.71 It is recognized that effect sizes of 0.2, 0.5, and 0.8 correspond to small, moderate, and large effects.73 Although there is no known research that establishes a cutoff of EMG activity (percentage of MVC) to be considered clinically relevant when comparing the EMG activity of different groups, it has been shown that EMG activity as low as 2% to 5% of MVC can be related to pain in neck-shoulder areas.85– 87 In addition, a minimally important difference for EMG activity has been found to be 2.9% of MVC.88 Although a large variability in the estimates of effect sizes was present in this data set (which had wide CIs), based on the calculated mean effect sizes (ie, standardized mean differences ranging between 0.41 and 0.66) and the raw mean differences obtained from the comparisons (ranging from 4.63% to 12.07% of MVC), differences in EMG activity were found in some of the comparisons between patients with TMD and the control group (Tab. 3). Thus, standardized effect sizes and minimally important difference could August 2011 serve as an index to guide clinicians in the relevance of the findings. It could be said that in the absence of knowledge and guidelines to determine the clinical relevance of certain outcomes, calculation of the clinical relevance, based on the distribution methods, could be an option. These results could be of importance for clinicians who work in this field because this analysis might indicate that patients with TMD tended to have increased activity of the superficial cervical muscles compared with the control group. In addition, the results of the subgroup analysis considering only patients with pure TMD provide more support for these findings. Furthermore, preliminary evidence has shown that exercises addressing these types of impairments (ie, training of neck flexor muscles) as part of cervical spine treatment in people with TMD reduced pain and improved function (ie, increased pain-free mouth opening) in patients with TMD, which potentially supports the fact that patients with TMD could benefit from treatment of impaired cervical flexor muscles.89 Therefore, these results might be considered when evaluating and treating patients with TMD. Nevertheless, it is necessary to implement a randomized controlled trial that addresses these cervical impairments through cervical flexor exercises in patients with TMD and test whether these exercises decrease pain and improve function and quality of life in patients with TMD. In this way, research could advance clinical practice in this area. Limitations The results obtained in this research are applicable for the group of individuals who participated in this study under the protocols used. They potentially could be applied to people with TMD having characteristics similar to those of the partici- pants in this study. This limitation should be taking into consideration when attempting to extrapolate these results. In addition, it must be acknowledged that because this project was cross-sectional, a causeand-effect relationship between cervical muscular impairment and TMD cannot be established. Conclusions There were no statistically significant differences (P⫽.07) in EMG activity in the SCM or the AS muscles in patients with mixed and myogenous TMD compared with individuals who were healthy when performing the CCFT. However, the patients with TMD tended to have increased activity of the superficial cervical muscles compared with the control group. This increased activity of the superficial muscles of the cervical spine might be associated with the neck disturbances seen in patients with TMD. This information may give clinicians insight into the importance of evaluation and possible treatment of the deep neck flexors in patients with TMD. However, future research should test the effectiveness of this type of program through a randomized controlled trial in individuals with TMD to determine the real value of treating this type of impairment in this population. Dr Armijo-Olivo, Dr Warren, Dr Major, and Dr Magee provided concept/idea/research design. Dr Armijo-Olivo, Mr da Costa, Dr Gadotti, Dr Major, Dr Thie, and Dr Magee provided writing. Dr Armijo-Olivo, Mr Fuentes, Mr da Costa, and Dr Gadotti provided data collection. Dr Armijo-Olivo and Dr Warren provided data analysis. Dr Armijo-Olivo and Dr Magee provided project management. Dr Armijo-Olivo provided fund procurement. Dr Magee provided facilities/ equipment and institutional liaisons. Dr Armijo-Olivo, Mr Fuentes, Mr da Costa, Dr Gadotti, Dr Warren, Dr Major, Dr Thie, and Dr Magee provided consultation (including review of manuscript before submission). The authors thank all of the participants in this study and Darrel Goertzen, Luis Cam- Volume 91 Number 8 Physical Therapy f 1195 Cervical Flexor Activity and Temporomandibular Disorders pos, and Rodrigo Guzman for their technical assistance. The study was approved by the Ethics Committee of the University of Alberta, Edmonton, Alberta, Canada. This research was presented at the XVIII International Conference of the International Society of Electrophysiology and Kinesiology, June 16 –19, 2010, Aalborg, Denmark; the 5th International Conference on Orofacial Pain and Temporomandibular Disorders, August 26 –30, 2009, Praia do Forte, Bahia, Brazil; and the 13th World Conference on Pain, August 29 –September 2, 2010, Montreal, Quebec, Canada. Dr Armijo-Olivo was supported by the Canadian Institutes of Health Research (CIHR), the Alberta Provincial CIHR Training Program in Bone and Joint Health, an Izaak Walton Killam Scholarship from the University of Alberta, and the Physiotherapy Foundation of Canada through an Ann Collins Whitmore Memorial Award. Mr Fuentes is supported by the government of Chile (BECAS Chile Scholarship Program) and Catholic University of Maule, Chile. DOI: 10.2522/ptj.20100233 References 1 De Leeuw R, ed. Orofacial Pain: Guidelines for Assessment, Diagnosis, and Management. 4th ed. Chicago, IL: Quintessence Publishing Co Inc; 2008:1–24. 2 McNeill C. Temporomandibular Disorders: Guidelines for Classification, Assessment, and Management. Chicago, IL: Quintessence Publishing Co Inc; 1993:12–30. 3 Drangsholt M, LeResche L. Temporomandibular disorder pain. In: Crombie I, Croft P, Linton S, et al, eds. Epidemiology of Pain. 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Pain. 2004;111: 245–252. 84 Kirk RE. Practical significance: a concept whose time has come. Educational Psychological Measurement. 1996;56:746 –759. 85 Veiersted KB, Westergaard RH, Andersen P. Pattern of muscle activity during stereotyped work and its relation to muscle pain. Int Arch Occup Environ Health. 1990;62: 31– 41. 86 Jonsson B. The static load component in muscle work. Eur J Appl Physiol Occup Physiol. 1988;57:305–310. 87 Jensen BR, Schibye B, Sogaard K, et al. Shoulder muscle load and muscle fatigue among industrial sewing-machine operators. Eur J Appl Physiol Occup Physiol. 1993;67:467– 475. 88 Armijo-Olivo S, Warren S, Fuentes J, Magee D. Clinical relevance vs. statistical significance: using neck outcomes in patients with TMD as an example. Man Ther. In press. 89 La Touche R, Fernandez-de-las-Penas C, Fernandez-Carnero J, et al. The effects of manual therapy and exercise directed at the cervical spine on pain and pressure pain sensitivity in patients with myofascial temporomandibular disorders. J Oral Rehabil. 2009;36:644 – 652. Volume 91 Number 8 Physical Therapy f 1197 Research Report Associations Between Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment: Gait Speed and the Timed “Up & Go” Test Ellen L. McGough, Valerie E. Kelly, Rebecca G. Logsdon, Susan M. McCurry, Barbara B. Cochrane, Joyce M. Engel, Linda Teri E.L. McGough, PT, PhD, Department of Rehabilitation Medicine, University of Washington, 1959 NE Pacific St, Box 356490, Seattle, WA 98195 (USA). Address all correspondence to Dr McGough at: [email protected]. V.E. Kelly, PT, PhD, Department of Rehabilitation Medicine, University of Washington. R.G. Logsdon, PhD, School of Nursing, University of Washington. S.M. McCurry, PhD, School of Nursing, University of Washington. B.B. Cochrane, PhD, RN, FAAN, School of Nursing, University of Washington. J.M. Engel, OT, PhD, FAOTA, Department of Occupational Sciences & Technology, University of Wisconsin–Milwaukee, Milwaukee, Wisconsin. L. Teri, PhD, School of Nursing, University of Washington. [McGough EL, Kelly VE, Logsdon RG, et al. Associations between physical performance and executive function in older adults with mild cognitive impairment: gait speed and the Timed “Up & Go” Test. Phys Ther. 2011;91: 1198 –1207.] © 2011 American Physical Therapy Association Published Ahead of Print: May 26, 2011 Accepted: March 22, 2011 Submitted: November 5, 2010 Background. Older adults with amnestic mild cognitive impairment (aMCI) are at higher risk for developing Alzheimer disease. Physical performance decline on gait and mobility tasks in conjunction with executive dysfunction has implications for accelerated functional decline, disability, and institutionalization in sedentary older adults with aMCI. Objectives. The purpose of this study was to examine whether performance on 2 tests commonly used by physical therapists (usual gait speed and Timed “Up & Go” Test [TUG]) are associated with performance on 2 neuropsychological tests of executive function (Trail Making Test, part B [TMT-B], and Stroop-Interference, calculated from the Stroop Word Color Test) in sedentary older adults with aMCI. Design. The study was a cross-sectional analysis of 201 sedentary older adults with memory impairment participating in a longitudinal intervention study of cognitive function, aging, exercise, and health promotion. Methods. Physical performance speed on gait and mobility tasks was measured via usual gait speed and the TUG (at fast pace). Executive function was measured with the TMT-B and Stroop-Interference measures. Results. Applying multiple linear regression, usual gait speed was associated with executive function on both the TMT-B (⫽⫺0.215, P⫽.003) and Stroop-Interference ( ⫽⫺0.195, P⫽.01) measures, indicating that slower usual gait speed was associated with lower executive function performance. Timed “Up & Go” Test scores (in logarithmic transformation) also were associated with executive function on both the TMT-B (⫽0.256, P⬍.001) and Stroop-Interference (⫽0.228, P⫽.002) measures, indicating that a longer time on the TUG was associated with lower executive function performance. All associations remained statistically significant after adjusting for age, sex, depressive symptoms, medical comorbidity, and body mass index. Limitations. The cross-sectional nature of this study does not allow for inferences of causation. Conclusions. Physical performance speed was associated with executive function after adjusting for age, sex, and age-related factors in sedentary older adults with aMCI. Further research is needed to determine mechanisms and early intervention strategies to slow functional decline. Post a Rapid Response to this article at: ptjournal.apta.org 1198 f Physical Therapy Volume 91 Number 8 August 2011 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment M ild cognitive impairment (MCI) is considered a transitional state that is less severe than dementia, but beyond that of typical age-related cognitive changes.1 Mild cognitive impairment is defined as impairment (adjusted for age and education) in one or more domains of cognition, with relative sparing of global cognitive functions.2– 4 Although MCI is associated with only mild decline in cognition, the onset of dementia is characterized by overt difficulties in multiple domains of cognitive function as well as performance of daily activities.2 Even in the presence of MCI, reduced function has been identified in executive function tasks,5,6 instrumental activities of daily living7,8 and physical performance tasks.9,10 There are 2 major subclassifications of MCI—amnestic MCI (aMCI) and nonamnestic MCI (naMCI)—the more common of which is aMCI.4,11 Older adults with aMCI, involving early memory loss, are at higher risk for Alzheimer disease (AD),4,11 and reduced executive function may be associated with early physical decline in people with aMCI. Identifying whether physical performance decline is associated with reduced executive function is important for developing physical therapy management strategies aimed at slowing the progression of functional decline and associated disability in older adults with aMCI. The worsening of executive function in older adults with aMCI is associated with the conversion to AD.5 The degenerative processes in aMCI involve medial temporal lobe structures, as observed in early stages of AD, but also may include the frontal lobe, the part of the brain involved in executive function.4,5 Executive function involves higher-order cognitive processes necessary for implementation of goal-directed behaviors,12 and reliance on executive function is elevated with increasing August 2011 difficulty of motor tasks,13,14 especially in novel or demanding situations.15 Medication adherence, cooking, housekeeping, and motor tasks performed in a complex environment are examples of goal-directed activities that are vulnerable to decline in executive function.12 Executive function is thought to rely strongly on the prefrontal cortex and includes multiple cognitive processes such as planning, tracking, judgment, initiation, scanning, sequencing, problem solving, and cognitive flexibility.12,16 The notion that executive function is multifaceted in nature is supported by evidence from functional magnetic resonance studies indicating that different aspects of executive function rely on different parts of the prefrontal cortex.17 Declining physical performance in conjunction with cognitive decline has been associated with increased risk for dementia and disability in population-based studies of older adults.18,19 In a prospective, longitudinal study of older adults who were healthy, slower self-selected gait speed was associated with cognitive impairment at the 6-year follow-up.20 In the Sydney Older Persons Study of people who did not have dementia at baseline, the presence of slowed gait speed in combination with cognitive deficits was associated with increased odds of progression to dementia.19 The combination of impaired physical performance and executive dysfunction may be more predictive of dementia risk; therefore, it has implications for accelerated functional decline, disability, and institutionalization in older adults with aMCI. Studies of physical performance in individuals with MCI support the notion that physical performance impairment is present prior to the onset of dementia,21,22 especially in older adults who demonstrate executive dysfunction.9,23 Executive dysfunction is predictive of functional decline and increased risk for dementia in community-dwelling older adults.24,25 Early pathology, consistent with AD, may contribute The Bottom Line What do we already know about this topic? Older adults with mild cognitive impairment (MCI) are at higher risk for dementia and associated disability. Functional decline often is accelerated in the presence of both physical and cognitive impairments. What new information does this study offer? In this study of sedentary older adults with amnestic MCI (memory loss), slower physical performance on gait and mobility tasks was associated with lower performance on executive function tasks, such as those involving planning and judgment. If you’re a patient or caregiver, what might these findings mean for you? Comprehensive prevention and rehabilitation strategies that enhance both cognitive and physical function are important in reducing functional decline and disability in older adults. Volume 91 Number 8 Physical Therapy f 1199 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment 28 presentations at independent retirement residences 890 telephone screening calls Not eligible (n=343): Too active=117 Health problem=93 Too young=27 No intervention group=60 Unavailable=46 Eligible for in-person screening (n=547) Completed in-person screening (n=359) Eligible, not interested (n=188) Not eligible after in-person screening (n=97): High cognition=37 Possible dementia=50 Health problem=10 Eligible for study (n=262) Completed baseline assessment (n=201) Figure. Flow chart of participant recruitment and screening. to physical performance impairment through alterations in memory, attention, and executive function networks.26,27 Alternatively, age and age-related comorbid conditions may be responsible for declining physical performance and executive dysfunction in older adults with memory impairment. It is unclear whether an association between physical performance and executive function remains after adjusting for age and age-related factors that are known to affect both physical performance and executive function in older adults with aMCI. Because older adults with both physical and cognitive impairment are at 1200 f Physical Therapy Volume 91 higher risk for dementia and disability,28 identifying whether physical performance decline is associated with executive dysfunction is important for developing physical therapy early intervention strategies for older adults with aMCI. The purpose of this study was to determine whether performance on 2 tests that are commonly used by physical therapists (usual gait speed and the Timed “Up & Go” Test [TUG]) are associated with performance on 2 neuropsychological tests of executive function (the Trail Making Test, part B [TMT-B], and Stroop-Interference, calculated from the Stroop Word Color Test) in sedentary older adults with aMCI after adjusting for age, Number 8 sex, depressive symptoms, medical comorbidity, and body mass index (BMI). We hypothesized that slower physical performance speed would be associated with lower executive function after adjusting for factors that are known to affect both physical performance and executive function. Method Participants This study involved analysis of baseline data from the Resources and Activities for Life-Long Independence (RALLI) Study, a longitudinal intervention study of cognitive function, aging, exercise, and health promotion in sedentary older adults with aMCI. Participants were volunteers living in independent retirement residences who reported mild memory problems. Study flyers were distributed, and a presentation was given to residents of 28 independent retirement living centers in the Seattle, Washington, metropolitan region. Residents who were interested in volunteering for the RALLI Study contacted the study coordinator (Figure). The sample size was determined based on a power analysis conducted for the randomized controlled trial. Participants enrolled in the study were aged 70 years and older, were sedentary, and were classified as having aMCI based on screening interviews and a consensus meeting. Study recruitment and screening consisted of: (1) a telephone screening interview, (2) an in-home screening evaluation that consisted of a semistructured interview and neuropsychological screening tests, and (3) an expert consensus panel to review screening data. Petersen criteria1,4 were applied using a combination of cognitive test scores, screening interview data, and consensus case review to identify people with memory problems that would be consistent with a clinical August 2011 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment subtype of aMCI (single or multiple domain). Petersen criteria included: (1) memory complaint, (2) impaired memory for age and education, (3) preserved general cognitive function, (4) essentially preserved activities of daily living, and (5) not already diagnosed with dementia. Participants were enrolled in the study from July 2007 through December 2009. Cognitive function tests and clinical criteria used to determine whether participants met the aMCI classification criteria included: (1) the MiniMental State Examination (MMSE) for global cognition,29 (2) the Wechsler Memory Scale–Revised (WMS-R) Logical Memory I and II subtests for immediate and delayed recall,30 and (3) the Clinical Dementia Rating Scale for severity rating of cognitive impairment.31 Memory impairment was determined by a Clinical Dementia Rating Scale score of 0.5 (consistent with MCI), a score on the WMS-R Logical Memory subtests that was 1 standard deviation below age- and education-adjusted norms,32 problems on the memory recall items of the MMSE, or observed difficulty with everyday recall during the assessment interview. Because the classification of aMCI involves a synthesis of information obtained through neuropsychological assessment, observations of daily activities, and clinical judgment,2,3 each participant was reviewed through a consensus process to determine eligibility for the study. The above neuropsychological test scores, performance on specific memory tasks, and evidence indicating intact ability to perform activities of daily living were examined by 2 clinical psychologists at a consensus meeting. Because aMCI is a clinical classification for which there is no single, definitive diagnostic test, a series of neuropsychological tests as well as an expert clinician’s observations and judgment are critical in identifying people at risk August 2011 for dementia.3 Sedentary lifestyle was defined as performance of less than 150 minutes of moderateintensity exercise per week (over the previous month), as recommended by the American College of Sports Medicine and the American Heart Association.33 Potential participants were excluded from the study if they: (1) did not meet aMCI criteria; (2) were unable to walk independently with an assistive device; (3) were expecting to move away from the area; (4) had a known terminal illness; (5) were actively suicidal, hallucinating, or delusional; (6) had been hospitalized within the previous 12 months; (7) had an uncontrolled chronic medical condition; (8) were blind or deaf; or (9) had a known central nervous system condition associated with dementia. Upon enrollment in the study, participants completed 2 in-home baseline evaluations administered by trained research assistants. During these evaluations, testing was completed for demographic and health-related information, physical performance measures, and executive function measures as described below. Each participant gave consent prior to the screening process. Demographic and HealthRelated Information Demographic and health-related information was collected via self-report responses. Medical comorbidity, assessed with the Self-Administered Comorbidity Questionnaire,34 was defined as having any of the following conditions: heart disease, hypertension, diabetes, pulmonary disease, kidney disease, peripheral vascular disease, osteoarthritis, rheumatoid arthritis, or back pain. Symptoms of depression were assessed using the Geriatric Depression Scale (range of scores⫽0 –15).35 Body mass index (kg/m2) was calculated using height and weight measured at baseline. Physical Performance Measures Usual gait speed was calculated from an 8-foot (approximately 2.4 m) walk test in which participants walked at their comfortable pace. The 8-foot walk test was completed inside the participant’s apartment or in a nearby hallway on a level surface with low-pile or indoor/outdoor carpet. The time to walk 8 feet was averaged over 2 trials and converted to gait speed (meters per second). Comfortable walking speed measurements have been reported to be highly reliable (r⫽.903) in individuals who were healthy and ranging in age from 20 to 79 years.36 Usual gait speed is comparable to the entire Short Physical Performance Battery in predicting disability in older adults.37 The TUG38 was performed at a fast pace to measure mobility speed.39 Participants were asked to move as quickly but as safely as possible to rise from an armchair (45.72-cm [18in] seat height), walk 3 m, turn around a cone, walk back to the chair, and sit down. Time to complete the TUG was averaged over 2 trials. When performed at a comfortable pace, TUG scores have good interrater and intrarater reliability as well as a high correlation with the Berg Balance Scale scores (r⫽⫺.81), gait speed (r⫽⫺.61) and Barthel Index of Activities of Daily Living scores (r⫽⫺.78), and normative values have been reported.36,40 When performed as quickly and as safely as possible, the TUG has demonstrated high sensitivity and specificity in identifying older adults who are prone to falling.39 Executive Function Measures The TMT-B was used to evaluate the components of executive function that represent complex visual scanning, speed, attention, and ability to shift sets.41,42 To complete this test, participants used a pencil to connect 25 encircled numbers and letters in Volume 91 Number 8 Physical Therapy f 1201 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment numerical and alphabetical order, alternating between numbers and letters.43 The maximum amount of time allowed to complete the TMT-B is 300 seconds; longer times indicate worse performance in executive function. The TMT-B has been widely used in studies of older adults, and normative data have been reported.44,45 The TMT-B was used in this study because it is considered to be specific to executive function processes due to its requirements for switching sets and mental tracking throughout the task.46 The Stroop Word Color Test was used to assess components of executive function representing a person’s ability to deal with conflicting stimuli.47 This test involves pairs of conflicting stimuli that are presented simultaneously, that is, the name of one color printed in another color. There are 3 portions to the Stroop Word Color Test: word naming (W), color naming (C), and color interference (CW). Although there are variations in test length and scoring methods,48,49 the version selected for this study involved recording the number of correct responses in 45 seconds for each portion of the test.50 A difference in the number of words printed in black ink compared with colors named correctly for words printed in a different color (ie, blue ink for the word “red”) is interpreted as interference of color stimuli. An overall Stroop-Interference score, as introduced by Golden,51 was calculated for this study using the formula: [CW ⫺ (W ⫻ C)/(W ⫹ C)]. In a previous study comparing older adults with aMCI with older adults with noncognitive impairments and mild AD, those with aMCI performed less well than those who were noncognitively impaired and better than the AD group on the color interference condition.52 Normative values for the raw scores from the 3 portions of the Stroop Word Color Test have been reported.44,53 1202 f Physical Therapy Volume 91 Data Analysis We used SPSS statistical software, version 16.0,* for descriptive statistics and data analysis. To examine the association between physical performance and components of executive function, linear regression was applied and model fit was evaluated. A curvilinear relationship was present between the TUG and executive function (both TMT-B and Stroop-Interference measures). With the understanding that the model is not intended for prediction, but rather to determine whether a relationship exists, we made the decision to log transform TUG scores. Upon transformation, we found that a linear relationship was present between log(TUG) and each executive function variable. To assess whether executive function, as measured by the TMT-B and Stroop-Interference, was associated with usual gait speed after adjusting for age, sex, depressive symptoms, medical comorbidity, and BMI, we created 2 multiple linear regression models. Covariates known to influence both walking speed and cognitive functions, including age, sex, depressive symptoms, medical comorbidity, and BMI, were entered into each model. The covariate variables were added first to each usual gait speed model, followed by the executive function variable. Although performance on the TMT-B and the Stroop Word Color Test have been associated with age and years of education in older adults,45,53 education was not included as a covariate in the multiple regression analysis because the majority of our sample had 12 years of more of education (97% had ⬎12 years of education, and 79.6% had ⬎13 years of education). To assess whether executive function, as measured by the TMT-B and * SPSS Inc, 233 S Wacker Dr, Chicago, IL 60606. Number 8 Stroop-Interference, was associated with the TUG after adjusting for covariates, 2 models were created using log(TUG) as the outcome. The same covariates as above were entered into each model because they are known to influence both mobility speed and cognitive functions. The covariate variables were added first to each TUG model, followed by the executive function variable. A dichotomous variable was created for comorbidity (none versus one or more medical conditions). Sex was coded 0 (male) or 1 (female). Correlations and the variance inflation factor for multicollinearity were used to identify whether covariates were strongly correlated. The contribution of the executive function variable in each model was assessed by the change in R2 values from the model with the covariates only to the model with the covariates and the executive function variable. Residual analysis for each multiple linear regression model included normal probability plots and scatter plots of standardized residuals. Role of the Funding Source Dr McGough received support through a National Institutes of Health Rehabilitation Sciences predoctoral fellowship (grant 2T32-HD00742416A1), a National Institute of Nursing Research/National Institutes of Health post-doctoral fellowship (grant T32 NR007106), and the de Tornyay Healthy Aging Doctoral Scholarship (School of Nursing, University of Washington). This work was supported by the National Institute on Aging/National Institutes of Health (grant 2RO1 AG1477706A2). Results Data for demographic and healthrelated variables are summarized in Table 1. Participants had a mean age of 84.6 years (SD⫽5.7), were 80.1% August 2011 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment female, and were 91% Caucasian. The initial sample was composed of 201 participants; however, 19 participants did not complete the TMT-B (16 due to vision problems and 3 due to missing data), and 25 participants did not complete the Stroop Word Color Test (22 due to vision problems or color blindness and 3 due to missing data). There also were missing data on the GDS (n⫽2), TUG (n⫽5), usual gait speed (n⫽2), MMSE (n⫽1), and logical memory (n⫽1). After accounting for all data entered into the multiple linear regression models, 179 cases were analyzed for associations between physical performance and the TMT-B, and 173 cases were analyzed for associations between physical performance and the StroopInterference measure. Sixteen participants (8.0% of the entire sample and 10.8% of those in the final analysis) reached the maximum time (300 seconds) on the TMT-B. Usual gait speed was statistically significantly associated with executive function in both the unadjusted analysis (Tab. 2) and after adjusting for covariates (Tab. 3). In the unadjusted analysis, usual gait speed was associated with the TMT-B (⫽⫺.267, P⬍.001) and Stroop-Interference (⫽⫺.214, P⫽.004) measures. The change in R2 values attributed to executive function was .07 for the TMT-B and .05 for the StroopInterference measure. After adjusting for covariates, the TMT-B (⫽⫺.215, P⫽.003) and StroopInterference (⫽⫺.195, P⫽.01) findings were statistically significant, indicating that slower usual gait speed was associated with lower executive function performance on both measures. The change in R2 values attributed to the addition of the TMT-B (the difference between the full model and the model with covariates only) was .044. The overall change in R2 values was .084; therefore, the full model explained 54.5% August 2011 Table 1. Descriptive Statisticsa n Mean (SD) or Percentage Minimum Age (y) 201 84.6 (5.7) 69.7 Sex, % female 201 80.1 Ethnicity, % Caucasian 201 91.0 % living alone 201 68.7 % high school education 201 97.5 Characteristic Maximum Demographic 104.3 Physical performance and executive function Gait speed (m/s) 199 0.61 (0.18) 0.24 1.08 TUG (s) 196 11.96 (5.54) 5.20 35.70 TUG (log) 196 1.041 (0.17) Trail Making Test, part B 182 148.04 (70.35) 0.716 Stroop-Interference 176 ⫺81.09 (20.78) Geriatric Depression Scale 199 2.48 (2.37) 0 12 WMS-R Logical Memory I 200 19.9 (7.5) 5.0 42.0 WMS-R Logical Memory II 200 14.1 (7.6) 0 35.0 MMSE 200 26.47 (2.56) % CDR 0.5 200 100.0 % BMI ⱖ25 kg/m2 201 59.9 % medical comorbidity 201 77.6 47.0 ⫺139.00 1.553 300.0b ⫺23.00 Clinical 18.00 30.00 a TUG⫽Timed “Up & Go” Test; TMT-B⫽Trail Making Test, part B; WMS-R⫽Wechsler Memory Scale– Revised; MMSE⫽Mini-Mental State Examination; CDR⫽Clinical Dementia Rating Scale; BMI⫽body mass index. b 10.8% of participants (n⫽16) reached the maximum TMT-B time of 300 seconds. more variance than the unadjusted model. The change in R2 attributed to the addition of the StroopInterference measure to the model was .034. The overall change in R2 values was .102; therefore, the full model explained 67.1% more of the variance than the unadjusted model. In the full model for usual gait speed, age and depressive symptoms were statistically significant when the TMT-B and Stroop-Interference measures were in the models, with slower usual gait speed associated with older age and depressive symptoms. Log(TUG) was statistically significantly associated with executive function in both the unadjusted anal- Table 2. Linear Regression for Usual Gait Speed and Timed “Up & Go” Test (TUG) (Log Transformed) Executive Function Physical Performance Trail Making Test, Part B (nⴝ180) Stroop-Interference Measure (nⴝ174) Usual gait speed (m/s) ⫽⫺.267, P⬍.001 (R2⫽.07) ⫽⫺.214, P⫽.004 (R2⫽.05) Log(TUG) ⫽.290, P⬍.001 (R ⫽.08) ⫽.251, P⫽.001 (R2⫽.06) 2 Volume 91 Number 8 Physical Therapy f 1203 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment Table 3. Linear Regression for Gait Speed (m/s) Standardized Coefficient () P Age ⫺.199 .007 Sex ⫺.08 .27 Depressive symptoms ⫺.182 .01 .057 .42 Explanatory Variable and Covariates Model 1 (n⫽179) Medical comorbidity Model 2 (n⫽173) Body mass index ⫺.09 .22 .110 Trail Making Test, part B ⫺.215 .003 .154b Age ⫺.173 .03 Sex ⫺.124 .09 Depressive symptoms ⫺.232 .002 Medical comorbidity a R 2a .081 .26 Body mass index ⫺.071 .35 .118 Stroop-Interference ⫺.195 .01 .152b F 5.25 (P⬍.001) 5.00 (P⬍.001) 2 The R value for the model not including the executive function variable. Change in R2 value was statistically significant at the .05 level when adding the executive function variable to the model. b ysis (Tab. 2) and after adjusting for covariates (Tab. 4). In the unadjusted analysis, log(TUG) was associated with the TMT-B (⫽.290, P⫽⬍ .001) and Stroop-Interference (⫽.251, P⫽.001) measures. The change in R2 values attributed to the executive function variable was .08 for the TMT-B and .06 for the StroopInterference measure. Log(TUG) was associated with both executive function measures after adjusting for covariates. The TMT-B (⫽.256, P⬍.001) and Stroop-Interference Table 4. Linear Regression for Timed “Up & Go” Test (Log Transformed) Explanatory Variable and Covariates Model 1 (n⫽178) Age .173 P .051 .45 Depressive symptoms .217 .002 ⫺.009 R 2a F .02 Sex Medical comorbidity Model 2 (n⫽173) Standardized Coefficient () .90 Body mass index .264 ⬍.001 .148 Trail Making Test, part B .256 ⬍.001 .211b Age .156 .05 7.66 (P⬍.001) Examination of multicollinearity among the explanatory variables using the variance inflation factor resulted in values close to 1, indicating no collinearity. Analysis of residuals for each model using normal q-plots and scatter plots of residuals by the estimated values showed that the model fit the data appropriately. .097 .18 Discussion Depressive symptoms .245 .001 In this study of sedentary older adults with aMCI, an association between physical performance speed and executive function on the TMT-B and Stroop-Interference measures was demonstrated after adjusting for age, sex, depressive symp- ⫺.036 .61 Body mass index .198 .008 .104 Stroop-Interference .228 .002 .147b a 5.96 (P⬍.001) The R2 value for the model not including the executive function variable. b Change in R2 value was statistically significant at the .05 level when adding the executive function variable to the model. f The results indicate that a longer time to complete the TUG was associated with lower executive function, that is, a longer time to perform the TMT-B and higher StroopInterference scores. The change in R2 values attributed to the addition of the TMT-B to the model was .063 (the difference between the full model and the model with covariates only). The overall change in R2 values was .13; therefore, the full model explained 61.6% more variance than the unadjusted model. The change in R2 values attributed to the addition of the Stroop-Interference measure to the model was .043. The overall change in R2 values was .087; therefore, the full model explained 59.2% more of the variance than the unadjusted model. In the full models for log(TUG), age, depressive symptoms, and BMI were statistically significant covariates, with higher values of log(TUG) (and, therefore, slower performance on the TUG) associated with higher values of BMI and depressive symptoms. Sex Medical comorbidity 1204 (⫽.228, P⫽.002) findings were statistically significant after adjusting for the other variables, indicating that slower TUG times were associated with lower executive function performance on both measures. Physical Therapy Volume 91 Number 8 August 2011 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment toms, and BMI. Slower usual walking speed was associated with lower performance on a test of mental flexibility (TMT-B) and with reduced ability to manage conflicting stimuli (Stroop-Interference). Similarly, performance on a functional mobility task (TUG at fast pace) was associated with both measures of executive function. The results of this study demonstrate a consistent relationship between 2 commonly used physical therapy assessment tools and 2 measures of executive function. This finding is clinically relevant in older adults with memory impairment because impairments in physical and cognitive domains increase the risk for accelerated functional decline and disability, especially in the presence of executive dysfunction.24 The prevalence of slowed gait speed is evident when working memory is challenged in older adults with MCI,54 thus supporting the notion that gait is not entirely automatic, but instead requires attentional resources.13,55 Physical performance is particularly challenged when older adults are asked to concurrently perform a cognitive task, suggesting that allocation of attention is necessary in older adults with and without cognitive impairment.56 Associations between physical performance and cognitive function have been reported in previous studies in the areas of gait speed, balance, and fall risk in older adults with MCI,9,57 and they are especially robust in the presence of executive dysfunction.23 Declining executive function may be an early indicator of overall functional decline in older adults. For example, in a prospective study of older women with intact cognition at baseline, executive function decline occurred 3 years prior to memory decline over a 9-year follow-up period, and executive function decline occurred more often than any other cognitive impairment.58 Sedentary August 2011 older adults with aMCI may be particularly vulnerable to executive function and mobility impairment and, therefore, at higher risk for subsequent functional decline and falls. Slowed physical performance may be a compensatory strategy to maintain accuracy in older adults with aMCI.59 People with MCI performed daily activities at slower speeds, but maintained accuracy on a series of daily activities.60 Older adults with probable AD who were asked to perform a cognitive task (repeating random digits) while walking demonstrated slower walking and greater variability in their walking pattern, possibly due to reduced ability to divide or prioritize attention.55 A similar phenomenon may be occurring in older adults with aMCI, with a slowing of task speed in an effort to maintain accuracy even under conditions of relatively low cognitive or environmental challenge, as implemented in our study. Therefore, older adults with aMCI may be particularly vulnerable to physical performance decline and fall risk on tasks that require attention and learning, such as attending to a new walking route or other nonroutine activities. Although age and age-related comorbid conditions may contribute to declining physical performance and executive dysfunction in older adults with memory impairment, the statistically significant associations that remain after adjusting for these factors in our study suggest that other mechanisms, such as brain pathology, may be contributing to this relationship. Medial temporal lobe structures, which are responsible for memory and learning, are the first brain regions affected by AD pathology, followed by other cortical and subcortical regions with disease progression.61,62 Pathology consistent with AD has been reported in the brains of older adults with aMCI63 and may contribute to physical performance impairment through alterations in memory, attention, and executive function networks.26,27 Alternatively, in older adults with aMCI, pathological mechanisms associated with declining physical performance may result from pathology not typically associated with AD, but instead with other dementia syndromes (eg, Parkinson disease, vascular disease) that interfere with frontalsubcortical circuits.27,64 Therefore, further research is needed to identify neuropathological mechanisms involved in the association between physical performance speed and executive dysfunction in older adults with aMCI. This study had a defined sample of sedentary older adults with aMCI and valid and reliable measures of physical performance and executive function. There were, however, several limitations. A ceiling effect on the TMT-B occurred with 8.0% of participants (final analysis) reaching the 300-second maximum, so we lack an estimate of the slowest performance possible on the TMT-B. The crosssectional nature of this study does not allow for inferences of causation. Nevertheless, consistent associations were demonstrated, suggesting that combining physical performance and executive function assessments may be clinically useful in detecting early functional decline in older adults with MCI. Although efforts were made to minimize bias through the selection of valid tests, consideration of potential confounders, and recruitment practices,65 a potential source of bias remains because this sample of older adults was recruited from independent retirement living centers. Future longitudinal studies to assess the predictive value of executive function measures on physical performance in people with aMCI are needed. Volume 91 Number 8 Physical Therapy f 1205 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment Conclusions Slower physical performance was associated with lower executive function in our sample of sedentary older adults with aMCI, and associations remained statistically significant after adjusting for age, sex, depressive symptoms, medical comorbidity, and BMI. Slower gait and mobility associated with reduced executive function in sedentary older adults with aMCI have implications for accelerated functional decline, disability, and institutionalization. Further research is needed to determine mechanisms for this association and whether early intervention strategies are effective in slowing functional decline and disability in sedentary older adults with aMCI. Early intervention strategies that focus on enhancing executive function as well as physical performance (eg, exercise) should be studied in sedentary older adults with aMCI. Dr McGough, Dr Kelly, Dr Logsdon, Dr McCurry, and Dr Teri provided concept/ idea/research design. All authors provided writing. Dr McGough, Dr Logsdon, Dr McCurry, and Dr Teri provided data collection. Dr McGough, Dr McCurry, and Dr Teri provided data analysis. Dr Logsdon, Dr McCurry, and Dr Teri provided project management, fund procurement, participants, and facilities/equipment. Dr Teri provided institutional liaisons. Dr Kelly, Dr Logsdon, Dr McCurry, Dr Cochrane, Dr Engel, and Dr Teri provided consultation (including review of manuscript before submission). The authors thank the Northwest Research Group on Aging, Ken Pike, PhD, for statistical support, and June van Leynseele, MA, for study coordination. The University of Washington Institutional Review Board approved the study procedures. A poster presentation of this research was given at the Combined Sections Meeting of the American Physical Therapy Association; February 17–20, 2010; San Diego, California. Dr McGough received support through a National Institutes of Health Rehabilitation Sciences predoctoral fellowship (grant 2T32HD-00742416A1), a National Institute of Nursing Research/National Institutes of 1206 f Physical Therapy Volume 91 Health post-doctoral fellowship (grant T32 NR007106), and the de Tornyay Healthy Aging Doctoral Scholarship (School of Nursing, University of Washington). This work was supported by the National Institute on Aging/National Institutes of Health (grant 2RO1 AG14777-06A2). DOI: 10.2522/ptj.20100372 References 1 Petersen RC, Smith GE, Waring SC, et al. Mild cognitive impairment: clinical characterization and outcome [erratum in: Arch Neurol. 1999;56:760]. Arch Neurol. 1999;56:303–308. 2 Gauthier S, Reisberg B, Zaudig M, et al. Mild cognitive impairment. 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Memory and executive function in aging and AD: multiple factors that cause decline and reserve factors that compensate. Neuron. 2004;44:195–208. 27 Tekin S, Cummings JL. Frontal-subcortical neuronal circuits and clinical neuropsychiatry: an update. J Psychosom Res. 2002; 53:647– 654. 28 von Bonsdorff M, Rantanen T, Laukkanen P, et al. Mobility limitations and cognitive deficits as predictors of institutionalization among community-dwelling older people. Gerontology. 2006;52:359 –365. 29 Folstein MF, Folstein SE, McHughs PR. “Mini-mental state”: a practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12: 189 –198. 30 Weschler D. Weschler Memory Scale. 3rd ed. In: Corporation TP (ed.). San Antonio, TX: The Psychological Corporation; 1997. August 2011 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment 31 Hughes CP, Berg L, Danziger WL, et al. A new clinical scale for the staging of dementia. Br J Psychiatry. 1982;140: 566 –572. 32 Steinberg BA, Bieliauskas LA, Smith GE, Ivnik RJ. Mayo’s older Americans normative studies: age- and IQ-adjusted norms for the Wechsler memory scale—revised. Clin Neuropsychol. 2005;19:378 – 463. 33 Nelson ME, Rejeski WJ, Blair SN, et al. Physical activity and public health in older adults: recommendation from the American College of Sports Medicine and the American Heart Association. Med Sci Sports Exerc. 2007;39:1435–1445. 34 Sangha O, Stucki G, Liang MH, et al. The Self-administered Comorbidity Questionnaire: a new method to assess comorbidity for clinical and health services research. Arthritis Rheum. 2003;49:156 –163. 35 Yesavage JA, Brink TL, Rose TL, et al. Development and validation of a geriatric depression screening scale: a preliminary report. J Psychiatr Res. 1982;17:37– 49. 36 Bohannon RW. Comfortable and maximum walking speed of adults aged 20 –79 years: reference values and determinants. Age Ageing. 1997;26:15–19. 37 Guralnik JM, Ferrucci L, Pieper CF, et al. Lower extremity function and subsequent disability: consistency across studies, predictive models, and value of gait speed alone compared with the short physical performance battery. J Gerontol A Biol Sci Med Sci. 2000;55:M221–M231. 38 Podsiadlo D, Richardson S. The timed “Up & Go”: a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc. 1991;39:142–148. 39 Shumway-Cook A, Brauer S, Woollacott M. Predicting the probability for falls in community-dwelling older adults using the Timed Up & Go Test. Phys Ther. 2000; 80:896 –903. 40 Steffen TM, Hacker TA, Mollinger L. Ageand gender-related test performance in community-dwelling elderly people: SixMinute Walk Test, Berg Balance Scale, Timed Up & Go Test, and gait speeds. Phys Ther. 2002;82:128 –137. 41 Reitan RM, Herring S. A short screening device for identification of cerebral dysfunction in children. J Clin Psychol. 1985; 41:643– 650. 42 Greenlief CL, Margolis RB, Erker GJ. Application of the Trail Making Test in differentiating neuropsychological impairment of elderly persons. Percept Mot Skills. 1985; 61(3 pt 2):1283–1289. August 2011 43 Bowie CR, Harvey PD. Administration and interpretation of the Trail Making Test. Nat Protoc. 2006;1:2277–2281. 44 Steinberg BA, Bieliauskas LA, Smith GE, Ivnik RJ. Mayo’s older Americans normative studies: age- and IQ-adjusted norms for the Trail Making Test, the Stroop Test, and MAE Controlled Oral Word Association Test. Clin Neuropsychol. 2005;19: 329 –377. 45 Zalonis I, Kararizou E, Triantafyllou NI, et al. A normative study of the Trail Making Test A and B in Greek adults. Clin Neuropsychol. 2008;22:842– 850. 46 Arbuthnott K, Frank J. Trail Making Test, part B as a measure of executive control: validation using a set-switching paradigm. J Clin Exp Neuropsychol. 2000;22: 518 –528. 47 Stroop JR. Studies of interference in serial verbal reaction. J Exp Psychol. 1936;18: 634 – 662. 48 Van der Elst W, Van Boxtel MP, Van Breukelen GJ, Jolles J. The Stroop ColorWord Test: influence of age, sex, and education; and normative data for a large sample across the adult age range. Assessment. 2006;13:62–79. 49 Valentijn SA, van Boxtel MP, van Hooren SA, et al. Change in sensory functioning predicts change in cognitive functioning: results from a 6-year follow-up in the Maastricht Aging Study. J Am Geriatr Soc. 2005;53:374 –380. 50 Golden CJ, Freshwater SM. Stroop Color and Word Test: A Manual for Clinical and Experimental Uses. Wood Dale, IL: Stoelting Co; 2002. 51 Golden CJ. Identification of brain disorders by the Stroop Color and Word Test. J Clin Psychol. 1976;32:654 – 658. 52 Kramer JH, Nelson A, Johnson JK, et al. Multiple cognitive deficits in amnestic mild cognitive impairment. Dement Geriatr Cogn Disord. 2006;22:306 –311. 53 Zalonis I, Christidi F, Bonakis A, et al. The stroop effect in Greek healthy population: normative data for the Stroop Neuropsychological Screening Test. Arch Clin Neuropsychol. 2009;24:81– 88. 54 Montero-Odasso M, Bergman H, Phillips NA. Dual-tasking and gait in people with mild cognitive impairment: the effect of working memory. BMC Geriatr. 2009; 9:41. 55 Sheridan PL, Solomont J, Kowall N, Hausdorff JM. Influence of executive function on locomotor function: divided attention increases gait variability in Alzheimer’s disease. J Am Geriatr Soc. 2003;51: 1633–1637. 56 Kelly VE, Schrager MA, Price R, et al. Ageassociated effects of a concurrent cognitive task on gait speed and stability during narrow-base walking. J Gerontol A Biol Sci Med Sci. 2008;63:1329 –1334. 57 Eggermont LH, Gavett BE, Volkers KM, et al. Lower-extremity function in cognitively healthy aging, mild cognitive impairment, and Alzheimer’s disease. Arch Phys Med Rehabil. 2010;91:584 –588. 58 Carlson MC, Xue QL, Zhou J, Fried LP. Executive decline and dysfunction precedes declines in memory: the Women’s Health and Aging Study II. J Gerontol A Biol Sci Med Sci. 2009;64:110 –117. 59 Scherder E, Eggermont L, Swaab D, et al. Gait in ageing and associated dementias; its relationship with cognition. Neurosci Biobehav Rev. 2007;31:485– 497. 60 Wadley VG, Okonkwo O, Crowe M, RossMeadows LA. Mild cognitive impairment and everyday function: evidence of reduced speed in performing instrumental activities of daily living. Am J Geriatr Psychiatry. 2008;16:416 – 424. 61 Braak H, Braak E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol. 1991;82:239 –259. 62 Braak H, Alafuzoff I, Arzberger T, et al. Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry. Acta Neuropathol. 2006;112:389 – 404. 63 Petersen RC, Parisi JE, Dickson DW, et al. Neuropathologic features of amnestic mild cognitive impairment. Arch Neurol. 2006; 63:665– 672. 64 Blahak C, Baezner H, Pantoni L, et al. Deep frontal and periventricular age related white matter changes but not basal ganglia and infratentorial hyperintensities are associated with falls: cross-sectional results from the LADIS study. J Neurol Neurosurg Psychiatry. 2009;80:608 – 613. 65 Portney LG, Watkins WM. Foundations of Clinical Research Applications to Practice. 3rd ed. Upper Saddle River, NJ: Pearson Education Inc; 2009. Volume 91 Number 8 Physical Therapy f 1207 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment Invited Commentary Teresa Y. Liu-Ambrose In their study,1 McGough and colleagues demonstrated that both usual gait speed and Timed “Up & Go” Test performance was significantly associated with executive functions, after accounting for age, sex, depressive symptoms, medical comorbidity, and body mass index, in a group of sedentary older adults with memory-based mild cognitive impairment (MCI). Their study highlights the co-occurrence of cognitive and physical decline in the clinical condition of MCI and reminds all of us of the complexity of geriatric rehabilitation. Mild cognitive impairment is a wellrecognized risk factor for both dementia2 and functional dependence.3,4 It is distinct from dementia and is conceptually defined as a clinical entity that is characterized by cognitive decline greater than that expected for an individual’s age and education level but that does not notably interfere with activities of daily living.2,5 It should be noted that MCI exists across a cognitive continuum with borders that are difficult to define precisely.2 Furthermore, there is considerable etiological and clinical heterogeneity within MCI. However, given the consequences of MCI, it is an important clinical entity that requires timely recognition and intervention. Of particular relevance to the practice of physical therapy, McGough and colleagues showed that older adults with MCI have increased risk for functional decline. Functional decline is associated with progressive loss of independence, reduced quality of life, greater risk for institutionalization, and increased mortality.6 –9 Older adults with MCI are at a higher risk for functional decline in part due to their increased risk for 1208 f Physical Therapy Volume 91 falls. Previous studies have demonstrated that older adults with MCI have impaired balance and gait10 –13 as well as impaired executive functions14 –16; each of these impairments is associated with falls.17 For example, Anstey and colleagues18 found that among older adults without cognitive impairment and dementia, baseline cognitive performance in the domain of executive functions was inversely associated with rate of falls over an 8-year period. McGough and colleagues extend these findings by highlighting the independent association among gait speed, mobility, and executive functions in this population of older adults who are at significant risk for dementia. In the last 5 years or so, there has been a growing recognition that physical function and cognitive function are interrelated. Evidence from neuroimaging studies provides insight into possible underlying mechanisms for this association. Specifically, cerebral white matter lesions (or leukoaraiosis) are associated with both reduced executive functions19 and gait and balance abnormalities.20 –23 Cerebral white matter lesions may interrupt frontal lobe circuits responsible for normal gait and balance or they may interfere with long loop reflexes mediated by deep white matter sensory and motor tracts.22 In addition, the periventricular and subcortical distribution of white matter lesions could interrupt the descending motor fibers arising from medial cortical areas, which are important for lowerextremity motor control.23 It is important to note that many of the pathological changes in the brain (eg, white matter lesions, reduced frontal-subcortical volume) associated with reduced executive functioning are clinically silent, but nev- Number 8 ertheless prevalent in the senior population.19 Thus, clinicians should be aware that reduced executive functioning is prevalent even among community-dwelling older adults without a formal diagnosis of cognitive impairment.24,25 Executive functions are higher-order cognitive processes that control, integrate, organize, and maintain other cognitive abilities.26 These cognitive processes are essential to a person’s ability to carry out healthpromoting behaviors,27 such as medication management, dietary and lifestyle changes, self-monitoring of responses, and follow-up with health care professionals. Maintaining executive functions is strongly associated with the ability to perform instrumental activities of daily living28 –33 and to live independently without assistance.34,35 Thus, to optimally prevent functional decline, McGough and colleagues’ work emphasizes the need for physical therapists to consider cognitive function—in particular, executive functions—in their management of older adults with impaired gait and mobility. Currently, balance and resistance training exercises are commonly prescribed by physical therapists to improve balance and mobility in older adults. However, given the associations among gait speed, mobility, and executive functions, it is time for physical therapists to prescribe exercise to optimize executive functions. Current evidence suggests that targeted aerobic exercise training36 or progressive resistance training37 has specific benefits for executive functions. Importantly, a recent study demonstrated that targeted aerobic exercise training can significantly improve executive func- August 2011 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment tions in older adults with amnestic MCI.38 Other potential strategies for enhancing executive functions include cognitive training.39 Finally, to ensure optimal rehabilitation uptake and adherence, physical therapists must work with older adults to overcome the barriers imposed by reduced executive functions. For example, they should include family members or close friends to facilitate uptake, use fridge magnets to remind the older adult the frequency and duration of prescribed exercises, provide easy-toread manuals that clearly illustrate specific exercises, and provide calendars to track exercise adherence and progression. In summary, the work of McGough and colleagues reinforces the notion that for rehabilitation strategies to effectively promote functional independence, they must be comprehensive in approach and not focus solely on physical function. T.Y. Liu-Ambrose, PT, PhD, Centre for Hip Health, Vancouver Coastal Health Research Institute, and Department of Physical Therapy, University of British Columbia, 3572647 Willow St, Vancouver, British Columbia, Canada V5Z 3P1. Address all correspondence to Dr Liu-Ambrose at: [email protected]. DOI: 10.2522/ptj.20100372.ic References 1 McGough EL, Kelly VE, Logsdon RG, et al. Associations between physical performance and executive function in older adults with mild cognitive impairment: gait speed and the Timed “Up & Go” Test. Phys Ther. 2011;91:1198 –1207. 2 Feldman HH, Jacova C. Mild cognitive impairment. Am J Geriatr Psychiatry. 2005;13:645– 655. 3 Royall DR, Lauterbach EC, Kaufer D, et al. The cognitive correlates of functional status: a review from the Committee on Research of the American Neuropsychiatric Association. J Neuropsychiatry Clin Neurosci. 2007;19:249 –265. August 2011 4 Wadley VG, Crowe M, Marsiske M, et al. Changes in everyday function in individuals with psychometrically defined mild cognitive impairment in the Advanced Cognitive Training for Independent and Vital Elderly Study. J Am Geriatr Soc. 2007;55:1192–1198. 5 Petersen RC, Doody R, Kurz A, et al. Current concepts in mild cognitive impairment. Arch Neurol. 2001;58:1985–1992. 6 Hunderfund AL, Roberts RO, Slusser TC, et al. Mortality in amnestic mild cognitive impairment: a prospective community study. Neurology. 2006;67:1764 –1768. 7 Markson EW. Functional, social, and psychological disability as causes of loss of weight and independence in older community-living people. Clin Geriatr Med. 1997;13:639 – 652. 8 Barberger-Gateau P, Fabrigoule C. Disability and cognitive impairment in the elderly. Disabil Rehabil. 1997;19:175–193. 9 Ramos LR, Simoes EJ, Albert MS. Dependence in activities of daily living and cognitive impairment strongly predicted mortality in older urban residents in Brazil: a 2-year follow-up. J Am Geriatr Soc. 2001; 49:1168 –1175. 10 Franssen EH, Souren LE, Torossian CL, et al. Equilibrium and limb coordination in mild cognitive impairment and mild Alzheimer’s disease. J Am Geriatr Soc. 1999; 47:463– 469. 11 Aggarwal NT, Wilson RS, Beck TL, et al. Motor dysfunction in mild cognitive impairment and the risk of incident Alzheimer disease. Arch Neurol. 2006;63: 1763–1769. 12 Kluger A, Gianutsos JG, Golomb J, et al. Patterns of motor impairement in normal aging, mild cognitive decline, and early Alzheimer’s disease. J Gerontol B Psychol Sci Soc Sci. 1997;52:P28 –P39. 13 Kluger A, Gianutsos JG, Golomb J, et al. Motor/psychomotor dysfunction in normal aging, mild cognitive decline, and early Alzheimer’s disease: diagnostic and differential diagnostic features. Int Psychogeriatr. 1997;9(suppl 1):307–316; discussion 317–321. 14 Wylie SA, Ridderinkhof KR, Eckerle MK, et al. Inefficient response inhibition in individuals with mild cognitive impairment. Neuropsychologia. 2007;45:1408 – 1419. 15 Backman L, Jones S, Berger AK, et al. Cognitive impairment in preclinical Alzheimer’s disease: a meta-analysis. Neuropsychology. 2005;19:520 –531. 16 Albert MS, Moss MB, Tanzi R, et al. Preclinical prediction of AD using neuropsychological tests. J Int Neuropsychol Soc. 2001; 7:631– 639. 17 Rapport LJ, Hanks RA, Millis SR, et al. Executive functioning and predictors of falls in the rehabilitation setting. Arch Phys Med Rehabil. 1998;79:629 – 633. 18 Anstey KJ, von Sanden C, Luszcz MA. An 8-year prospective study of the relationship between cognitive performance and falling in very old adults. J Am Geriatr Soc. 2006;54:1169 –1176. 19 Thal DR, Del Tredici K, Braak H. Neurodegeneration in normal brain aging and disease. Sci Aging Knowledge Environ. 2004;2004:pe26. 20 Briley DP, Wasay M, Sergent S, et al. Cerebral white matter changes (leukoaraiosis), stroke, and gait disturbance. J Am Geriatr Soc. 1997;45:1434 –1438. 21 Soumare A, Elbaz A, Zhu Y, et al. White matter lesions volume and motor performances in the elderly. Ann Neurol. 2009; 65:706 –715. 22 Masdeu JC, Wolfson L, Lantos G, et al. Brain white-matter changes in the elderly prone to falling. Arch Neurol. 1989;46: 1292–1296. 23 Baloh RW, Ying SH, Jacobson KM. A longitudinal study of gait and balance dysfunction in normal older people. Arch Neurol. 2003;60:835– 839. 24 Boone KB, Miller BL, Lesser IM, et al. Performance on frontal lobe tests in healthy older individuals. Dev Neuropsychol. 1990;6:215–223. 25 Royall DR. Prevalence of executive control function (ECF) impairment among healthy non-institutionalized retirees: the Freedom House Study. Gerontologist. 1998;38S:314 –315. 26 Stuss DT, Alexander MP. Executive functions and the frontal lobes: a conceptual view. Psychol Res. 2000;63:289 –298. 27 Kuo HK, Lipsitz LA. Cerebral white matter changes and geriatric syndromes: is there a link? J Gerontol A Biol Sci Med Sci. 2004; 59:818 – 826. 28 Grigsby J, Kaye K, Baxter J, et al. Executive cognitive abilities and functional status among community-dwelling older persons in the San Luis Valley Health and Aging Study. J Am Geriatr Soc. 1998;46: 590 –596. 29 Cahn-Weiner DA, Malloy PF, Boyle PA, et al. Prediction of functional status from neuropsychological tests in communitydwelling elderly individuals. Clin Neuropsychol. 2000;14:187–195. 30 Bell-McGinty S, Podell K, Franzen M, et al. Standard measures of executive function in predicting instrumental activities of daily living in older adults. Int J Geriatr Psychiatry. 2002;17:828 – 834. 31 Royall DR, Palmer R, Chiodo LK, et al. Declining executive control in normal aging predicts change in functional status: the Freedom House Study. J Am Geriatr Soc. 2004;52:346 –352. 32 Royall DR, Chiodo LK, Polk MJ. Correlates of disability among elderly retirees with “subclinical” cognitive impairment. J Gerontol A Biol Sci Med Sci. 2000;55:M541–M546. 33 Royall DR, Palmer R, Chiodo LK, et al. Executive control mediates memory’s association with change in instrumental activities of daily living: the Freedom House Study. J Am Geriatr Soc. 2005;53: 11–17. 34 Royall DR, Chiodo LK, Polk MJ. An empiric approach to level of care determinations: the importance of executive measures. J Gerontol A Biol Sci Med Sci. 2005;60: 1059 –1064. Volume 91 Number 8 Physical Therapy f 1209 Physical Performance and Executive Function in Older Adults With Mild Cognitive Impairment 35 Royall DR, Cabello M, Polk MJ. Executive dyscontrol: an important factor affecting the level of care received by older retirees. J Am Geriatr Soc. 1998;46:1519 –1524. 36 Colcombe SJ, Kramer AF, Erickson KI, et al. Cardiovascular fitness, cortical plasticity, and aging. Proc Natl Acad Sci U S A. 2004;101:3316 –3321. We thank Liu-Ambrose for her commentary1 on our work related to physical performance and executive function in older adults with mild cognitive impairment.2 The associations between cognition and physical function in older adults with and without clinically defined cognitive impairment have important implications for physical therapy management strategies. Given the associations between executive function and instrumental activities of daily living,3,4 observations of everyday activities provide clinically relevant information for physical therapists and may serve as early signs of functional decline.5 In addition, impairments in other cognitive domains, such as memory, require involvement of caregivers and use of memory aids to achieve ongoing exercise participation at an optimal dose. Physical therapy strategies that address physical, cognitive, environmental, and social barriers are necessary for achieving an optimal f Physical Therapy Volume 91 39 Willis SL, Tennstedt SL, Marsiske M, et al. Long-term effects of cognitive training on everyday functional outcomes in older adults. JAMA. 2006;296:2805–2814. Ellen L. McGough, Valerie E. Kelly, Rebecca G. Logsdon, Susan M. McCurry, Barbara B. Cochrane, Joyce M. Engel, Linda Teri Author Response 1210 37 Liu-Ambrose T, Nagamatsu LS, Graf P, et al. Resistance training and executive functions: a 12-month randomized controlled trial. Arch Intern Med. 2010;170: 170 –178. 38 Baker LD, Frank LL, Foster-Schubert K, et al. Effects of aerobic exercise on mild cognitive impairment: a controlled trial. Arch Neurol. 2010;67:71–79. response to exercise interventions in older adults with and without clinically defined cognitive impairment. As noted in our study and in the commentary by Liu-Ambrose, cognitive and physical functioning are associated in older adults, including those with mild cognitive impairment, and these impairments respond to physical therapy interventions. Early intervention strategies aimed at enhancing executive function through aerobic and strengthening interventions are warranted for improving gait function and reducing fall risk.1,6 Indeed, our own intervention research7 indicates functional gains even among those older adults with dementia. The potential for physical therapy to improve the lives of older adults is clear. We look forward to continued progress in this area and continued dialogue. DOI: 10.2522/ptj.20100372.ar Number 8 References 1 Liu-Ambrose TY. Invited commentary on “Associations between physical performance and executive function in older adults with mild cognitive impairment: gait speed and the Timed ‘Up & Go’ Test.” Phys Ther. 2011;91:1208 –1210. 2 McGough EL, Kelly VE, Logsdon RG, et al. Associations between physical performance and executive function in older adults with mild cognitive impairment: gait speed and the Timed “Up & Go” Test. Phys Ther. 2011;91:1198 –1207. 3 Farias ST, Mungas D, Reed BR, et al. MCI is associated with deficits in everyday functioning. Alzheimer Dis Assoc Disord. 2006; 20:217–223. 4 Johnson JK, Lui LY, Yaffe K. Executive function, more than global cognition, predicts functional decline and mortality in elderly women. J Gerontol A Biol Sci Med Sci. 2007;62:1134 –1141. 5 Wadley VG, Okonkwo O, Crowe M, RossMeadows LA. Mild cognitive impairment and everyday function: evidence of reduced speed in performing instrumental activities of daily living. Am J Geriatr Psychiatry. 2008;16:416 – 424. 6 Liu-Ambrose T, Davis JC, Nagamatsu LS, et al. Changes in executive functions and self-efficacy are independently associated with improved usual gait speed in older women. BMC Geriatr. 2010;10:25. 7 Teri L, Gibbons LE, McCurry SM, et al. Exercise plus behavioral management in patients with Alzheimer disease: a randomized controlled trial. JAMA. 2003;290:2015–2022. August 2011 Research Report A. Glässel, PT, BSc, MSc, MPH, Swiss Paraplegic Research, Nottwil, Switzerland, and ICF Research Branch in cooperation with the WHO Collaborating Centre for the Family of International Classifications in Germany (DIMDI). Content Validity of the Extended ICF Core Set for Stroke: An International Delphi Survey of Physical Therapists Andrea Glässel, Inge Kirchberger, Barbara Kollerits, Edda Amann, Alarcos Cieza Background. The “Extended ICF Core Set for stroke” is an application of the International Classification of Functioning, Disability and Health (ICF) and represents the typical spectrum of problems in functioning of people with stroke. I. Kirchberger, PhD, MPH, Institute for Health and Rehabilitation Sciences (IHRS), LudwigMaximilian University, Munich, Germany, and ICF Research Branch in cooperation with the WHO Collaborating Centre for the Family of International Classifications in Germany (DIMDI). Design and Methods. Physical therapists experienced in stroke intervention B. Kollerits, PhD, MPH, Institute for Health and Rehabilitation Sciences (IHRS), Ludwig-Maximilian University, and ICF Research Branch in cooperation with the WHO Collaborating Centre for the Family of International Classifications in Germany (DIMDI). were asked about their patients’ problems and resources and about aspects of the environment that physical therapists treat in people with stroke in a 3-round electronic-mail survey using the Delphi technique. The responses were linked to the ICF. The degree of agreement was calculated using the kappa statistic. E. Amann, PhD, MPH, Institute for Health and Rehabilitation Sciences (IHRS), Ludwig-Maximilian University. Objective. The objective of this study was to validate this ICF Core Set from the perspective of physical therapists. Results. One hundred twenty-five physical therapists from 24 countries named 4,793 problems treated by physical therapists in people with stroke. They identified 10 second-level ICF categories that currently are not represented in the Extended ICF Core Set for stroke. Twelve responses of the participants were linked to the ICF component personal factors, and 15 responses were not covered by the current version of the classification. The kappa coefficient for the linking agreement was 0.39 (95% bootstrapped confidence interval⫽0.34 – 0.41). Limitations. Two World Health Organization regions were not represented in the sample of physical therapists. Conclusions. According to the physical therapists, the current version of the Extended ICF Core Set for stroke largely covers the types of problems that their interventions address. However, some aspects of functioning emerged that are not yet covered and may need further investigation. A. Cieza, PhD, MPH, Institute for Health and Rehabilitation Sciences (IHRS), Ludwig-Maximilian University, Marchioninistrasse 17, 81377 Munich, Germany; Swiss Paraplegic Research, Nottwil, Switzerland; and ICF Research Branch in cooperation with the WHO Collaborating Centre for the Family of International Classifications in Germany (DIMDI). Address all correspondence to Dr Cieza at: [email protected]. [Glässel A, Kirchberger I, Kollerits B, et al. Content validity of the Extended ICF Core Set for stroke: an international Delphi survey of physical therapists. Phys Ther. 2011;91:1211–1222.] © 2011 American Physical Therapy Association Published Ahead of Print: June 9, 2011 Accepted: March 29, 2011 Submitted: August 12, 2010 Post a Rapid Response to this article at: ptjournal.apta.org August 2011 Volume 91 Number 8 Physical Therapy f 1211 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective A nnually about 15 million people worldwide experience a stroke.1 Although stroke is one of the leading causes of mortality, 40% to 77% of those affected are still alive 1 year after the event.2 One third of the survivors face long-term disability. Disability after stroke appears in the form of neurological dysfunctions (eg, motor, sensory, visual), limited ability to perform activities of daily living (ADL), and neuropsychological deficits (memory, attention, language).3 Taking the diversity and complexity of consequences of a stroke into account, an interdisciplinary approach is most appropriate. Rehabilitation after stroke requires an interprofessional team including physicians, psychologists, occupational therapists, nurses, social workers, and physical therapists.4,5 Physical therapists are described as one of the key components of the interdisciplinary team in stroke rehabilitation.6 – 8 Particularly, physical therapy aims at restoring motor control in locomotion, improving upperlimb function, enhancing the ability of people with stroke to cope with existing deficits in ADL, and achieving the best possible participation in the community. In order to reach these rehabilitation goals, physical therapists use different neurological intervention approaches and instruct and advise people with stroke and their families regarding prevention of complications, such as falls and shoulder pain.9,10 To optimize interventions aimed at improving function and minimizing disability, a proper understanding of an individual’s functioning and health status is needed.4 The World Health Organization’s International Classification of Functioning, Disability and Health (ICF)11 is based on an integrative model of health that provides a holistic, multidimensional, and interdisciplinary under1212 f Physical Therapy Volume 91 standing of health and health-related conditions. According to the ICF, the problems associated with a disease may concern body functions and body structures and the performance of activities and participation in life situations. Health states and the development of disability are modified by contextual factors, including environmental factors and personal factors.11 The ICF comprises 1,454 categories from the components body functions, body structures, activities and participation, and environmental factors, which are organized in a hierarchical structure (Fig. 1). Categories are divided into chapters, which constitute the first level of specification. Higher-levels categories (eg, second, third, or fourth level) are more detailed. Both the content and the structure of the ICF point out the potential value for rehabilitation professions, especially physical therapy.5 The ICF is increasingly applied in physical therapy and rehabilitation, especially in the field of neurorehabilitation, to facilitate interdisciplinary team communication, to structure the rehabilitation process, for goal setting and assessment, and for documentation and reporting.12,13 Recently, ICFbased documentation tools have been developed for use in interdisciplinary rehabilitation management.14 However, the ICF as a whole is not feasible for use in routine clinical application. To facilitate the implementation of the ICF into clinical practice, “ICF Core Sets” have been developed.15,16 The ICF Core Sets include a selection of ICF categories relevant for people with a specific health condition or a specific intervention phase (eg, acute or postacute care).15 The development of the ICF Core Set followed a standard approach that included a formal decision-making and consensus process integrating evidence gathered from preparatory studies by expert Number 8 neurologic health care professionals. Preparatory studies included a worldwide Delphi study with 36 experts, including 7 physical therapists; a systematic review of outcome measures used in 160 stroke clinical trials; and an empiric data collection on 93 German patients with stroke.17–19 Based on the results of these studies, a panel of 36 stroke experts (25 physicians, 7 physical therapists, 2 psychologists, 1 social worker, and 1 sociologist) from 12 different countries decided on the composition of the “Comprehensive ICF Core Set for stroke” in a formal consensus process. The Comprehensive ICF Core Set for stroke includes a set of 130 ICF categories that cover the typical spectrum of problems in functioning in people with chronic stroke.20 It was extended by 36 ICF categories from the ICF Core Sets for people with neurological conditions in the acute and early postacute phases to enable its use it in all clinical situations.20,21 Based on this Extended ICF Core Set for stroke, physical therapists can comprehensively describe the impairments, limitations in activities, restriction in participation, and influential environmental factors of a determined person with stroke and can create a functioning profile. The Extended ICF Core Set for stroke can facilitate assessment and offers the opportunity to clarify responsibilities among the team members by distributing the information gathered from specific ICF categories to the appropriate team members.13,22 The Extended ICF Core Set for stroke is now undergoing worldwide testing using a number of approaches, including international multicenter field studies, reliability studies,23 and content validation from the health care professional perspective. Content validity from the health care professional perspective means that at least those problems in functionAugust 2011 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective ICF Fuctioning and Disability Body Functions and Structures Activities and Participation Classification Contextual factors Parts Personal Factors Not classified Environmental Factors Components Categories b1-b8 s1-s8 d1-d9 e1-e5 Chapter/ 1st level b110b899 s110s899 d110d999 e110e599 2nd level b1100b7809 s1100s8309 d1550d9309 e1100e5959 3rd level b11420b54509 s11000s76009 4th level Figure 1. Structure of the World Health Organization’s International Classification of Functioning, Disability and Health (ICF). Reprinted with permission of the World Health Organization. All rights are reserved by the World Health Organization. ing that are substantial targets of the specific interventions applied by health care professionals are represented in the ICF Core Set for stroke. This is a prerequisite for the implementation of the ICF Core Set for stroke in clinical practice. For example, if joint mobility is a main intervention target of physical therapists, it is essential that physical therapists document the extent and the change of joint mobility problems in a determined patient during the treatment course using the ICF Core Set for stroke. Consequently, if the corresponding ICF category for joint mobility is not included in the current version of the Core Set for stroke, the Core Set is lacking content validity from the perspective of physical therapists. The purpose of this study was to examine the content validity of the Extended ICF Core Set for stroke from the perspective of physical therapists. The aims of this study August 2011 were: (1) to identify the patient’s problems, resources, and aspects of environment treated by physical therapists and (2) to analyze whether these issues are represented by the current version of the Extended ICF Core Set for stroke. Method A 3-round electronic-mail survey of physical therapists using the Delphi technique was conducted.24 –27 The purpose of the Delphi technique is to gain consensus from a panel of individuals who have knowledge of a topic being investigated.28 These informed people are commonly called experts.29 The Delphi method is a multistage process, with each stage building on the results of the previous one, and a series of rounds are used to both gather and provide information about a particular subject. The technique is characterized by its anonymity to avoid the dominance of single individuals in a group; by iteration, which allows panel members to change their opinions in subsequent rounds; and by controlled feedback, which shows the distribution of the group’s responses as well as each individual’s previous responses.30 Recruitment of Participants In the preparatory phase of the study, international associations of physical therapists, such as the World Confederation for Physical Therapy (WCPT) and members of the European Region of WCPT, as well as universities with health care professional programs and members of the Association of Higher Education of Physical Therapy (ENPHE) were contacted. Associations with a focus on neurorehabilitation and certified physical therapists in neurological intervention from United States received an invitation to participate. A literature search and personal recommendations were used to identify experts. Volume 91 Number 8 Physical Therapy f 1213 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective First Round Activities of study group The participants received an e-mail with general information and instructions as well as a questionnaire with the following open-ended question: “What are the patients’ problems, patients’ resources, and aspects of the environment treated by physical therapists in patients with stroke?” Activities of experts Creating a list of patients’ problems, patients’ resources, and aspects of the environment treated by physical therapists in patients with stroke • Linking of responses to ICF categories Second Round The participants received an e-mail with instructions and the questionnaire for the second round with the following question: “Do you agree that these ICF categories represent patients’ problems, patients’ resources, or aspects of the environment treated by physical therapists in patients with stroke?” Judgment (yes/no), whether the listed ICF categories reflect the treatment by physical therapists in patients with stroke • Calculation of frequencies (%) • Feedback of individual judgment • Feedback of group answer Third Round The participants received an e-mail with instructions and the questionnaire for the third round with the following question: “Taking into account the answers of the group and your individual answer in the second round, do you agree that these ICF categories represent patients’ problems, patients’ resources, or aspects of the environment treated by physical therapists in patients with stroke?” Judgment (yes/no), whether the listed ICF categories reflect the treatment by physical therapists in patients with stroke • Calculation of frequencies (%) Figure 2. Description of the Delphi exercise. 1214 f Physical Therapy Volume 91 Number 8 August 2011 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective The sample was selected using a purposive sampling approach, which is commonly applied in Delphi studies.25,31,32 Purposive sampling is based on the assumption that a researcher’s knowledge about the population can be used to handpick the cases to be included in the sample.33 In contrast to random sampling, purposive sampling does not ensure representativeness. Because no database of the target population of physical therapists worldwide who are experienced in the treatment of patients with stroke was available, random sampling was not possible in our study. To ensure that the participants were experienced in the management of people poststroke, the initial letter specified that participants should be “physical therapy experts in the treatment of poststroke individuals.” The first contact included an invitation to participate and a detailed description of the project’s targets, the Delphi process, and the time line. The study was conducted from January to August 2005. Delphi Process The process and verbatim questions of the electronic-mail survey using the Delphi technique are displayed in Figure 2. The participants had 3 weeks to mail their responses for each round. Reminders were sent 1 week and 2 days before the deadline and 1 week after the deadline. The study was conducted in the English language. In the first round of the Delphi procedure, an information letter including instructions and an Excel* file containing an open-ended questionnaire was sent to all participants. The participants were requested to list all of the “patients’ problems, patients’ resources, and aspects of environ* Microsoft Corporation, One Microsoft Way, Redmond, WA 98052-6399. August 2011 Figure 3. Scree test results for second Delphi round. Selection of International Classification of Functioning, Disability and Health (ICF) categories without clear consensus using the modified Scree test. The ICF categories of the second Delphi round were ordered by percentage of expert agreement and plotted. The Scree line was placed onto the slope, along the points to see where they approximately form a straight line. Points close to the Scree line indicate an inadequate endorsement. Cutpoints were defined as the points where the slope markedly deviated from the Scree line. The ICF categories with an agreement of ⬎25.2% and ⬍90.7% were included in the third Delphi round. ment treated by physical therapists in patients with stroke.” The phrasing of this question aimed at encouraging the participants to consider not only problems but also resources and environmental factors that are covered by the ICF model. The responses were collected and linked to the ICF. Additionally, the participants were asked to complete questions on demographic characteristics and professional experience. In the second Delphi round, the participants received a list of the ICF categories linked to the responses of the first round. The participants were requested to agree or disagree that the respective ICF category represents patients’ problems, patients’ resources, or aspects of the environment treated by physical therapists in patients with stroke. Again, the number of participants considering the listed ICF categories as relevant was calculated. In order to maintain the participants’ motivation and increase the response rates, the participants of the third Delphi round received only a selection of ICF categories included in the second round. The Scree test was used to identify the categories that did not reach an adequate consensus.34,35 The Scree test includes an examination of a graph of the percentage of agreement among the participants plotted along the vertical axis against the ICF categories plotted along the horizontal axis. A straightedge is placed along the points to see where they form an approximately straight line, the Scree line. Points close to the Scree line indicated an insufficient endorsement (Fig. 3). The participants Volume 91 Number 8 Physical Therapy f 1215 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective received a list of the selected ICF categories, including the proportion and the identification numbers of the participants who had agreed that the categories represent patients’ problems, patients’ resources, or aspects of the environment treated by physical therapists in individuals after stroke. The participants were requested to answer the same question taking into account the answers of the group, as well as their previous response. Linking An ICF category is coded by the component letter and a suffix of 1 to 5 digits. The letters b, s, d, and e refer to the components body functions (b), body structures (s), activities and participation (d) and environmental factors (e) (Fig. 1). This letter is followed by a 1-digit number indicating the chapter, the code for the second level (2 digits), and the codes for the third and fourth levels (1 digit each). The component letter with the suffixes of 1, 3, 4, or 5 digits corresponds to the code of the ICF categories. Within each component, the categories are arranged in a stem/branch/leaf scheme. This scheme indicates that a moredetailed, higher-level category covers all the aspects applicable for the lower-level category, of which it is a member, but not vice versa. Each response from the first Delphi round was linked to the most precise ICF category based on 10 linking rules established in a previous study.36 If an answer contained more than one concept, several ICF categories could be linked. Answers related to personal factors were assigned the code “pf.” If the content of an answer was not included in the ICF classification, this answer was coded “not covered.” The linking was performed by a physical therapist (A.G.) who specialized in stroke intervention. In addition, responses from 46 partici1216 f Physical Therapy Volume 91 pants (36.8%) out of the 125 participants were linked independently by a psychologist (E.A., B.K.). The people involved in the linking process had some years of experience regarding the ICF. Because the linking process is extremely timeconsuming and the linking of a sample of the 4,793 responses was expected to provide a good estimation of the true agreement, we refrained from linking all responses. Consensus between the physical therapist and the psychologist was used to decide which ICF category should be linked to each response. In cases of disagreement between the health care professionals, the suggested categories were discussed by a team consisting of psychologists (E.A., B.K., I.K.) and a physical therapist (A.G.) aimed at a joint decision. Statistical Methods Statistical analysis was performed using SAS for Windows, version 6.† Descriptive statistics were used to characterize the sample and frequencies of responses. The agreement between the individuals who performed the linking was described using the percentage of agreement and kappa statistics with bootstrapped confidence intervals.37,38 The values of the kappa coefficient generally range from 0 to 1, where 1 indicates perfect agreement and 0 indicates no additional agreement beyond what is expected by chance only. The percentage of participants who agreed with the question of the second and third Delphi rounds was calculated. Only ICF categories that reached consensus among the participants in the third round were considered for comparison with the Extended ICF Core Set for stroke. Lacking a universally accepted definition of consensus,31 an agreement of at least 75% among the participants was considered sufficiently high, based on experiences in previous studies.16,31 Results Recruitment and Participants Seventy-eight national physical therapy associations and 54 European associations named 23 participants. Three participants were named by the European Federation of NeuroRehabilitation (EGNR). Seventeen certified experts in neurology from the United States agreed to participate. Nine universities with specialization in neurology named 11 participants, and 6 Bobath instructors agreed to participate. Two participants were identified by literature searches. Thirty-two international and 8 national partners from the ICF Network for stroke were contacted. Five of them agreed to participate. The remaining 80 physical therapists who participated in this study were contacted on the basis of personal recommendations of other participants (“snowball sampling”). In total, 146 physical therapists from 24 countries agreed to participate. One hundred twenty-five (85.6%) out of 146 physical therapists who agreed to participate in the study completed the first-round questionnaire. The demographic and professional characteristics of these participants are shown in Table 1. Delphi Process In the first Delphi round, 4,793 patients’ problems, patients’ resources, or aspects of the environment treated by physical therapists in patients with stroke were named. One hundred eleven out of 125 participants (88.8%) filled in the second round questionnaire. One hundred one (90.9%) out of 111 physical therapists completed the third-round questionnaire. † SAS Institute Inc, 100 SAS Campus Dr, Cary, NC 27513-2414. Number 8 August 2011 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective Table 1. Distribution of the Participants About 3 Delphi Rounds and Demographic and Professional Experience of the Participants From Round 1a Professional Experience (y), Median (Range) Practical Experience With Patients With Stroke (y), Median (Range) Self-rating Stroke Treatment Expertisec (y), Median (Range) Round 1 (n) Round 2 (n) Round 3 (n) % Female Age (y), Median (Range) Regions of the Americas 28 25 23 85.10 39.0 (31.0–51.0) 15.0 (6.0–30.0) 13.0 (5.0–28.0) 4.0 (3.0–5.0) European region 91 81 73 80.20 42.0 (22.0–67.0) 16.0 (1.0–40.0) 13.0 (1.0–35.0) 4.0 (3.0–5.0) 4 3 3 100.00 43.5 (28.0–47.0) 21.5 (6.0–25.0) 16.5 (3.0–25.0) 4.0 (3.0–4.0) 4.25 (4.0–4.5) WHO Regionb Western Pacific region African region Total 2 2 2 50.00 51.5 (35.0–68.0) 26.5 (11.0–42.0) 26.5 (13.0–40.0) 125 (87.4%) 111 (88.8%) 101 (90.9%) 77.9% 40.0 (22–68) 16.0 (1–42) 13.0 (1–40) 4.0 (3–5) a WHO⫽World Health Organization. Region of Americas: Brazil, Canada, Jamaica, and United States; European region: Austria, Belgium, Czech Republic, Finland, Germany, Hungary, Israel, Italy, Netherlands, Norway, Spain, Sweden, Switzerland, Turkey, and United Kingdom; Western Pacific region: Australia, Japan, and New Zealand; African region: Nigeria and South Africa; Eastern Mediterranean region: not represented; South East Asia region: not represented. c 1⫽low, 5⫽excellent. b Linking of the Responses to the ICF All components of the ICF were represented by 376 identified ICF categories. Seven fourth-level categories, 80 third-level categories, and 59 second-level categories were linked to the component body functions. Two fourth-level categories, 12 thirdlevel categories, and 10 second-level categories were linked to the component body structures. Sixty-seven third-level categories and 53 secondlevel categories were linked to the component activities and participation. Twenty-seven third-level categories and 37 second-level categories were linked to the component environmental factors. Fifteen aspects were named that could be attributed to the not-yet-developed ICF component personal factors. Fifteen responses were not covered by the current version of the ICF. Agreement between the 2 people who performed the linking was reached in 42% of the responses. The kappa value for the linking was 0.39, with a 95% bootstrapped confidence interval of 0.34 to 0.41. August 2011 Representation of the Physical Therapists’ Responses in the ICF Core Set for Stroke In total, from the 376 ICF categories linked to the participants’ responses, 185 reached an agreement of at least 75% in the final round and were considered for comparison with the Extended ICF Core Set for stroke. Of the 83 ICF categories linked to body functions, 26 are included on the same level of classification and 48 are more-detailed third- and fourth-level categories, which are represented by the corresponding second-level categories (eg, “b1300 Energy level,” which is represented in the Extended ICF Core Set for stroke by the second-level category “b130 Energy and drive functions”) (Tab. 2). Ten ICF categories that correspond to the 4 second-level ICF categories “b445 Respiratory muscle function,” “b720 Mobility of joint functions,” “b765 Involuntary movement functions,” and “b780 Sensations related to muscles and movement functions” are not represented in the Extended ICF Core Set for stroke (Tab. 2). Of the component body structures, 23 ICF categories reached an agreement of ⱖ75%. Among these, 6 categories are included in the Extended ICF Core Set for stroke at the same level of classification, whereas 9 categories were represented at a different level of the classification. Three second-level ICF categories and 5 corresponding third-level categories are not represented in the Extended ICF Core Set for stroke (Tab. 2). Of the 67 ICF categories from the ICF component activities and participation that reached an agreement of ⱖ75%, 23 are included at the same level of the classification and 42 more-detailed, third-level categories are represented in the Extended ICF Core Set for stroke by their corresponding second-level categories. Two ICF categories, namely “d435 Moving objects with lower extremities” and “d6504 Maintaining assistive devices,” are not represented in the Extended ICF Core Set for stroke (Tab. 2). Of the component environmental factors, 9 categories reached an Volume 91 Number 8 Physical Therapy f 1217 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective Table 2. International Classification of Functioning, Disability and Health (ICF) Categories That Are Not Represented in the Current Version of the ICF Core Set for Stroke: Percentage of Participants Who Considered the Respective ICF Category as Relevant in the Final Round (Round 3)a ICF Code Level 2 ICF Code Level 3 Title of ICF Category Final Round (nⴝ101), % Body functions b445 Respiratory muscle functions b720 Mobility of bone functions 98.2 b765 Involuntary movement functions 93.6 b7650 Involuntary contractions of muscles 86.8 b7651 Tremor 92.9 Sensations related to muscles and movement functions 99.1 b7800 Sensation of muscle stiffness 98.1 b7801 Sensation of muscle spasm 95.5 Structure of pelvic region 90.7 b780 100.0 Body structures s740 Muscles of pelvic region 96.3 s760 s7402 Structure of trunk 92.5 s770 Additional musculoskeletal structures related to movement 94.0 s7700 Bones 89.5 s7701 Joints 96.3 s7702 Muscles 96.2 s7703 Extra-articular ligaments, fasciae, extramuscular aponeuroses, retinacula, septa, bursae, unspecified 90.7 Moving objects with lower extremities 98.2 Maintaining assistive devices 83.0 Assistive products and technology for culture, recreation, and sport 77.7 Activities and participation d435 d6504 Environmental factors e1401 a Only categories with agreement of ⱖ75% are shown. agreement of ⱖ75%. Of these, 5 categories are included at the same level of classification in the Extended ICF Core Set for stroke, whereas 3 categories were represented at a different level of the classification. The ICF category “e1401 Assistive products and technology for culture, recreation and sport” is not represented in the Extended ICF Core Set for stroke (Tab. 2). 1218 f Physical Therapy Volume 91 Twelve responses were assigned to the not-yet-developed ICF component personal factors and reached an agreement surpassing 75%. Most of them addressed attitudes supporting the independence of a person with stroke in managing his or her disease (eg, self-management, compliance, autonomy/independence). Autonomy, compliance, self-concept and self-management, illness knowl- Number 8 edge, and coping were considered to comprise personal factors according to the ICF language. In addition, “brain plasticity” and “recovery” were identified as personal factors representing relevant aspects of stroke intervention by physical therapists (Tab. 3). Fifteen responses of the participants were not covered by any ICF component or specific ICF category out of the classification (Tab. 3). Discussion This study examined the content validity of the Extended ICF Core Set for stroke from the perspective of physical therapists. In this study, content validity refers to the extent to which the patients’ problems, patients’ resources, and environmental factors identified by physical therapists as relevant to their management of people with stroke are represented in the Extended ICF Core Set for stroke. An agreement of at least 75% among the participants in the final Delphi round was regarded as sufficient consensus. Consequently, ICF categories with an agreement of at least 75% that are not represented in the Extended ICF Core Set for stroke may indicate missing content validity and will be the main focus of the following discussion. A 100% agreement among the participants was found regarding the category “b445 Respiratory muscle function.” However, this ICF category is not included in the Extended ICF Core Set for stroke. Several studies have demonstrated that problems associated with strength (forcegenerating capacity) and endurance of respiratory muscles, as well as with muscles of the trunk and the position of the diaphragm, are important risk factors for secondary complications after stroke such as pneumonia.39 In order to minimize these risks, physical therapists use respiratory exercises, including August 2011 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective training of respiration and specific intervention techniques, to activate or relax respiratory muscles.40 The participants addressed nearly all of the different categories from the ICF chapter “Neuro-musculosceletal and Movement-Related Functions,” which covers functions of joints, bones, reflexes, and muscles.11 These aspects clearly represent one main focus of the physical therapists’ work in stroke rehabilitation. However, although the ICF category “b720 Mobility of bone functions” reached an agreement of 98.2% among the participants, it is not included in the ICF Core Set for stroke. Bone mobility is a prerequisite for activities such as grasping a glass. Bone mobility is treated by physical therapists using different manual techniques (eg, mobilization of the scapulae in people with shoulder pain after stroke).41 Furthermore, more than 90% of the participants agreed that the ICF category “b765 Involuntary movement functions” is a problem treated by physical therapists, which is not included in the ICF Core Set for stroke. This finding is clearly supported by literature, which reports a close relationship between stroke and spasticity (hypertonicity) and the incidence of clonus or tremor.42,43 In addition, validation studies have identified this ICF category as being relevant for occupational therapists44 and physicians.45 Regarding the ICF category “b780 Sensations related to muscles and movement functions,” which is not represented in the ICF Core Set for stroke, again a high consensus among the participants was found. It is quite obvious that people with stroke experience stiffness and tightness of muscles. Muscle spasms and heaviness of muscles are commonly treated by physical therapists.40 August 2011 Table 3. Responses That Were Linked to the International Classification of Functioning, Disability and Health (ICF) Component Personal Factors and “Not Classified” Terms: Percentage of Participants Who Considered the Respective Concepts As Relevant in the Final Round (Round 3)a Final Round (nⴝ101), % Personal Factors Autonomy, independence 97.3 Brain plasticity/recovery 97.2 Self-concept, self-perception 95.9 Endurance/discipline, hardiness 93.8 Coping 92.8 Optimistic/positive attitude 92.8 Compliance 92.7 Self-management 91.8 Illness knowledge 91.8 Problems/worries/uncertainty about future 88.6 Sense of mastery 88.5 Life values, life goals, lifestyle 87.6 Final Round (nⴝ101), % Not Classified a Posture/postural alignment 99.1 Adaptation to bodily changes/compensation strategies 98.1 Secondary complications 98.1 Multiprofessional and interdisciplinary treatment 97.2 Therapeutic positioning 97.2 Assessment of the patient and evaluation 96.3 Impairment of body symmetry 96.3 Positive model for living with a handicap 95.8 Education of self and family about stroke 95.4 Physical therapy intervention 95.2 Perspective of life (living at home, profession) 92.7 Learning experience in dealing with limitations 92.7 Conveying problem to others and their understanding 91.8 Competence in self-relaxation 91.8 Self-observation 91.8 Only concepts with agreement of ⱖ75% are shown. With regard to the ICF component body structures, 3 ICF categories were found not to be included in the current version of the ICF Core Set for stroke. Spasticity and muscle imbalance in lower limbs, which are major problems after stroke, are associated with walking problems. Improvement of multijoint coordination and improvement of muscle activity in the lower limbs, including the pelvis, are relevant intervention goals for physical therapists. However, the ICF category “s740 Structure of pelvic region” is currently not included. The ICF category “s760 Structure of trunk,” including bones, muscles, and ligaments of the trunk, repre- Volume 91 Number 8 Physical Therapy f 1219 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective sents a main intervention area of physical therapy after stroke because hemiplegia not merely results in diverse problems in the upper and lower extremities but also affects the trunk and its corresponding structures.46,47 Finally, the ICF category “s770 Additional musculoskeletal structures related to movement” addresses structures that still are not sufficiently mapped in the ICF. For instance, muscles of the neck frequently are affected in neglect.48 Regarding the ICF component activities and participation, the ICF category “d435 Moving objects with lower extremities” was regarded as relevant by the participants, but this category is not included in the ICF Core Set for stroke. Indeed, people with stroke have impairments in structure and functioning of the feet, such as decreased muscle power or problems with spasticity or flaccid muscles, that can lead to difficulties with pushing pedals on a bicycle or pressing the gas pedal of a car.49,50 On the other hand, problems with riding a bicycle or driving a car are covered by the ICF category “d475 Driving,” which is already part of the Extended ICF Core Set for stroke. The high level of agreement among the participants regarding the ICF categories related to assistive devices such as “e115 Products and technology for personal use in daily living” highlights the relevance of a restoratory and compensatory rehabilitation strategy. Education and training on the use and maintenance of assistive devices are an inherent part of physical therapy. However, the ICF categories “e1401 Assistive products and technology for culture, recreation, and sport” and “d6504 Maintaining assistive devices” are not yet included in the Extended ICF Core Set for stroke. Twelve aspects were linked to the not-yet-developed ICF component 1220 f Physical Therapy Volume 91 personal factors. Patients’ selfmanagement, illness knowledge, and ability to cope with the disease are relevant for patient education provided by physical therapists.51 Various studies and systematic reviews support the positive effects of patient education regarding selfmanagement51 and coping with disease.52 These results indicate that personal factors also are considered by physical therapists. Therefore, it could be most helpful for physical therapists if the ICF would provide a classification of the personal factors in the future. This classification will enable health care professionals to identify systematically all personal factors influencing the functioning of a certain person. Posture/postural alignment was regarded as a relevant aspect by almost all of the participants; however, this aspect is not covered by the ICF. Although the ICF category “d415 Maintaining a body position” covers the static aspects of posture, the dynamic aspects of posture are missing. Thus, it could be useful to develop an ICF category addressing posture/postural alignment more specifically. However, when increasing the specificity of such an ICF category, it should be kept in mind that the ICF should be used by all health care professions and, therefore, physical therapy–specific terminology should be avoided. In general, the participants named a large number of detailed aspects, represented by third- and fourthlevel ICF categories, which are relevant for stroke intervention. This detailed information is necessary for assessment, therapy planning, and intervention in physical therapy. As the ICF Core Set includes only lessspecific, second-level categories, this detailed information might be unfavorable for physical therapist practice on the one hand. On the other hand, the current version of the Number 8 Extended ICF Core Set for stroke already includes 166 second-level ICF categories, and any further extension could compromise its feasibility in clinical practice. The Delphi technique proved to be an appropriate method for this study objective. With response rates exceeding 87% in the present study, previously reported response rates of approximately 50%30,33,53 were clearly surpassed. However, there are some limitations regarding the reliability and external validity of this study. The agreement between the people who performed the linking was lower than in other studies that used comparable methods.54 –56 This finding may be related to the fact that the answers of the participants were longer and, therefore, the extraction of the meaningful concepts was more difficult than in similar studies regarding other health conditions. Consequently, the instructions for the first round were revised for their use in future studies. Furthermore, as we have only linked a sample of the responses, we cannot exclude that the agreement would have been different in another sample of responses. Although we were successful in recruiting physical therapists from 24 countries, the African and Eastern Mediterranean world regions are not represented in the sample. Health care systems in these world regions may differ from those of other world regions, and it cannot be excluded that this difference also affects the intervention targets of physical therapists in stroke treatment. Thus, the sample is not representative of all physical therapists experienced in the intervention of people with stroke worldwide. Language barriers could have influenced the participation in some world regions because August 2011 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective the Delphi survey was conducted in English language only. Although some restrictions of the current version of the Extended ICF Core Set for stroke were detected in this study, we found the categories of the current version of the Extended ICF Core Set for stroke largely represent what the physical therapists in our study agreed upon to take care of in their interventions. The results of finalized or ongoing studies involving both health care professionals44,45 and patients will further elucidate the validity of the Extended ICF Core Set for stroke from the different perspectives. A number of ICF categories identified as missing in the current version of the Extended ICF Core Set for stroke by occupational therapists44 also were mentioned by the participants in our study. These ICF categories included “b720 Mobility of bone functions” and “b765 Involuntary movement functions” from the component body functions, “s760 Structure of trunk” and “s770 Additional musculoskeletal structures related to movement” from the component body structures, “d435 Moving objects with lower extremities” and “d650 Caring for household objects” from the component activities and participation, and “e140 Products and technology for culture, recreation, and sport” from the component environmental factors. In contrast to physical therapists and occupational therapists, physicians have found only 4 ICF categories that are relevant for their treatment but not yet part of the current version of the Extended ICF Core Set for stroke.45 Of interest, the ICF category “b765 Involuntary movement functions” was mentioned as relevant by all 3 health care professions. Thus, this category would be a good candidate for inclusion in the Extended ICF Core Set for stroke. August 2011 The validation from the perspective of 3 different health care professions has shown that it might be useful to add relevant ICF categories to the Extended ICF Core Set for stroke.44,45 On the other hand, studies that have applied the Extended ICF Core Set for stroke in a sample of people with stroke have identified ICF categories that are less relevant and might be excluded.57,58 However, the validation from the patient perspective is not yet completed. It seems reasonable that a final decision on the content of a revised version of the Extended ICF Core Set for stroke should be postponed until the results from the patient perspective are available and can be included in the discussion. All authors provided concept/idea/project design. Ms Glässel, Dr Kirchberger, and Dr Cieza provided writing. Ms Glässel provided data collection. Ms Glässel, Dr Kirchberger, Dr Kollerits, and Dr Amann provided data analysis. Ms Glässel and Dr Kirchberger provided project management. Dr Kirchberger and Dr Cieza provided consultation (including review of manuscript before submission). The authors thank the participants of the Delphi exercise for their valuable contribution and their time in responding to the questionnaires. This study forms part of Ms Glässel’s doctoral thesis at the Faculty of Medicine, LudwigMaximilian University, Munich, Germany. This research, in part, was presented at the 16th International Congress of the World Confederation for Physical Therapy; June 20 –33, 2011; Amsterdam, the Netherlands. The responsibility for the content of this publication lies within the ICF Research Branch. DOI: 10.2522/ptj.20100262 References 1 Murray CJ, Lopez AD. Mortality by cause for eight regions of the world: Global Burden of Disease Study. Lancet. 1997;349: 1269 –1276. 2 Kaste M, Fogelholm R, Rissanen A. Economic burden of stroke and the evaluation of new therapies. Public Health. 1998; 112:103–112. 3 Srikanth VK, Thrift AG, Saling MM, et al. Increased risk of cognitive impairment 3 months after mild to moderate first-ever stroke: a community-based prospective study of nonaphasic English-speaking survivors. Stroke. 2003;34:1136 –1143. 4 Stucki G, Ewert T, Cieza A. Value and application of the ICF in rehabilitation medicine [retraction in: Disabil Rehabil. 2009;31:425]. 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Using a case report of a patient with spinal cord injury to illustrate the application of the International Classification of Functioning, Disability and Health during multidisciplinary patient management. Phys Ther. 2010;90:1039 –1052. 15 Stucki G, Grimby G. Applying the ICF in medicine. J Rehabil Med. 2004;(44 suppl): 5– 6. 16 Cieza A, Ewert T, Üstün TB, et al. Development of ICF Core Sets for patients with chronic conditions. J Rehabil Med. 2004; (44 suppl):9 –11. Volume 91 Number 8 Physical Therapy f 1221 Extended ICF Core Set for Stroke From Physical Therapists’ Perspective 17 Geyh S, Kurt T, Brockow T, et al. Identifiying the concepts contained in the outcome measures of clinical trails on stroke using the International Classification of Functioning, Disability and Health as a reference. J Rehabil Med. 2004;(44 suppl):56 – 62. 18 Weigl M, Cieza A, Andersen C, et al. Identification of relevant ICF categories in patients with chronic health conditions: a Delphi exercise. J Rehabil Med. 2004;(44 suppl):12–21. 19 Ewert T, Fuessl M, Cieza A. Identification of the most common patient problems in patients with chronic conditions using the ICF checklist. J Rehabil Med. 2004;(44 suppl):22–29. 20 Geyh S, Cieza A, Schouten J, et al. ICF Core Sets for stroke. J Rehabil Med. 2004; (44 suppl):135–141. 21 Grill E, Lipp B, Boldt C, et al. Identification of relevant ICF categories by patients with neurological conditions in early post-acute rehabilitation facilities. Disabil Rehabil. 2005;27:459 – 465. 22 Steiner WA, Ryser L, Huber E, et al. Use of the ICF model as a clinical problemsolving tool in physical therapy and rehabilitation medicine. Phys Ther. 2002;82: 1098 –1107. 23 Starrost K, Geyh S, Trautwein A, et al. Interrater reliability of the extended ICF core set for stroke applied by physical therapists. Phys Ther. 2008;88:841– 851. 24 Duffield C. The Delphi technique: a comparison of results obtained using two expert panels. Int J Nurs Stud. 1993;30: 227–237. 25 Goodman CM. The Delphi technique: a critique. J Adv Nurs. 1987;12:729 –734. 26 Linstone HA, Turoff M. The Delphi Technique: Techniques and Applications. London, United Kingdom: Addison Wesley; 1975. 27 Williams PL, Webb C. The Delphi technique: a methodological discussion. J Adv Nurs. 1994;19:180 –186. 28 McKenna HP. The Delphi technique: a worthwhile research approach for nursing? J Adv Nurs. 1994;19:1221–1225. 29 Strauss H, Zeigler L. The Delphi technique and its uses in social science research. J Creat Behav. 1975;9:253–259. 30 Jones J, Hunter D. Consensus methods for medical and health services research. BMJ. 1995;311:376 –380. 31 Hasson F, Keeney S, McKenna HP. Research guidelines for the Delphi survey technique. J Adv Nurs. 2000;32:1008 – 1015. 32 Keeney S, Hasson F, McKenna HP. A critical review of the Delphi technique as a research methodology for nursing. Int J Nurs Studies. 2001;38:195–200. 1222 f Physical Therapy Volume 91 33 Polit DF, Hungler BP. Essentials of Nursing Research: Methods, Appraisal and Utilisation. New York, NY: Lippincott, Williams & Wilkins; 1997. 34 Zoski KW, Jurs S. Priority determination in surveys: an application of the Scree Test. Eval Rev. 1990;14:214 –219. 35 Race KE, Planek TW. Modified scree test: further considerations on its application to Delphi study data. Eval Rev.1992;16:171– 183. 36 Cieza A, Brockow T, Ewert T, et al. Linking health-status measurements to the International Classification of Functioning, Disability and Health. J Rehabil Med. 2002;34:205–210. 37 Vierkant RA. SAS macro for calculating bootstrapped confidence intervals about a Kappa coefficient. Available at: http:// www2.sas.com/proceedings/sugi22/STATS/ PAPER295.PDF. Accessed July 23, 2004. 38 Cohen J. A coefficient of agreement for nominal scales. Educ Psychol Meas. 1969; 20:46. 39 Indredavik B, Rohweder G, Naalsund E, Lydersen S. Medical complications in a comprehensive stroke unit and an early supported discharge service. Stroke. 2008; 39:414 – 420. 40 Guide to Physical Therapist Practice. 2nd ed. Phys Ther. 2001;81:9 –746. 41 Turner-Stokes L, Jackson D. Shoulder pain after stroke: a review of the evidence base to inform the development of an integrated care pathway. Clin Rehabil. 2002; 6:276 –298. 42 Wu CL, Huang MH, Lee CL, et al. Effect on spasticity after performance of dynamicrepeated-passive ankle joint motion exercise in chronic stroke patients. Kaohsiung J Med Sci. 2006;22:610 – 617. 43 Fraix V, Delalande I, Parrache M, et al. Action-induced clonus mimicking tremor. Mov Disord. 2008;23:285–288. 44 Glässel A, Kirchberger I, Linseisen E, et al. Content validation of the International Classification of Functioning, Disability and Health (ICF) Core Set for stroke: the perspective of occupational therapists. Can J Occup Ther. 2010;77:289 –302. 45 Lemberg I, Kirchberger I, Stucki G, Cieza A. The ICF Core Set for stroke from the perspective of physicians: a worldwide validation study using the Delphi technique. Eur J Phys Rehabil Med. 2010;46: 377–388. 46 Dickstein R, Shefi S, Marcovitz E, Villa Y. Anticipatory postural adjustment in selected trunk muscles in poststroke hemiparetic patients. Arch Phys Med Rehabil. 2004;85:261–267. Number 8 47 Hsieh CL, Sheu CF, Hsueh IP, Wang CH. Trunk control as an early predictor of comprehensive activities of daily living function in stroke patients. Stroke. 2002;85: 2626 –2630. 48 Schindler I, Kerkhoff G. Convergent and divergent effects of neck proprioceptive and visual motion stimulation on visual space processing in neglect. Neuropsychologia. 2004;42:1149 –1155. 49 Voller B, Földy D, Hefter H, et al. Treatment of the spastic drop foot with botulinum toxin type A in adult patients [article in German]. Wien Klin Wochenschr. 2001;113(suppl 4):25–29. 50 Janssen TW, Beltman JM, Elich P, et al. Effects of electric stimulation-assisted cycling training in people with chronic stroke. Arch Phys Med Rehabil. 2008;89: 463– 469. 51 Scottish Intercollegiate Guidelines Network (SIGN). Management of patients with stroke. Published November 2002. Available at: http://www.sign.ac.uk/pdf/ sign64.pdf. Accessed March 30, 2007. 52 Talbot LR, Viscogliosi C, Desrosiers J, et al. Identification of rehabilitation needs after a stroke: an exploratory study. Health Qual Life Outcomes. 2004;2:53. 53 Geschka H. Delphi. In: Bruckmann G, ed. Long-Term Prognosis. Wurzburg, Germany: Heibert; 1977. 54 Kirchberger I, Glaessel A, Stucki G, Cieza A. Validation of the comprehensive International Classification of Functioning, Disability and Health Core Set for rheumatoid arthritis: the perspective of physical therapists. Phys Ther. 2007;87:368 – 384. 55 Kirchberger I, Stamm T, Cieza A, Stucki G. Does the comprehensive ICF Core Set for rheumatoid arthritis capture occupational therapy practice: a content-validity study. Can J Occup Ther. 2007;74 Spec. No.: 267–280. 56 Kirchberger I, Cieza A, Stucki G. Validation of the comprehensive ICF Core Set for rheumatoid arthritis: the perspective of psychologists. Psychology & Health. 2008;23:639 – 659. 57 Algurén B, Lundgren-Nilsson A, Sunnerhagen KS. Facilitators and barriers of stroke survivors in the early post-stroke phase. Disabil Rehabil. 2009;31:1584 –1591. 58 Algurén B, Lundgren-Nilsson A, Sunnerhagen KS. Functioning of stroke survivors: a validation of the ICF Core Set for stroke in Sweden. Disabil Rehabil. 2010;32: 551–559. August 2011 Research Report Association of Body Mass Index With Self-Report and Performance-Based Measures of Balance and Mobility Andrea L. Hergenroeder, David M. Wert, Elizabeth S. Hile, Stephanie A. Studenski, Jennifer S. Brach Background. The incidence of obesity is increasing in older adults, with associated worsening in the burden of disability. Little is known about the impact of body mass index (BMI) on self-report and performance-based balance and mobility measures in older adults. Objective. The purposes of this study were (1) to examine the association of BMI with measures of balance and mobility and (2) to explore potential explanatory factors. Design. This was a cross-sectional, observational study. Methods. Older adults (mean age⫽77.6 years) who participated in an ongoing observational study (N⫽120) were classified as normal weight (BMI⫽18.5–24.9 kg/m2), overweight (BMI⫽25.0 –29.9 kg/m2), moderately obese (BMI⫽30.0 –34.9 kg/m2), or severely obese (BMIⱖ35 kg/m2). Body mass index data were missing for one individual; thus, data for 119 participants were included in the analysis. Mobility and balance were assessed using self-report and performance-based measures and were compared among weight groups using analysis of variance and chi-square analysis for categorical data. Multiple linear regression analysis was used to examine the association among BMI, mobility, and balance after controlling for potential confounding variables. Results. Compared with participants who were of normal weight or overweight, those with moderate or severe obesity were less likely to report their mobility as very good or excellent (52%, 55%, 39%, and 6%, respectively); however, there was no difference in self-report of balance among weight groups. Participants with severe obesity (n⫽17) had the lowest levels of mobility on the performance-based measures, followed by those who were moderately obese (n⫽31), overweight (n⫽42), and of normal weight (n⫽29). There were no differences on performance-based balance measures among weight groups. After controlling for age, sex, minority status, physical activity level, education level, and comorbid conditions, BMI still significantly contributed to mobility (⫽⫺.02, adjusted R2⫽.41). Conclusions. Although older adults with severe obesity were most impaired, those with less severe obesity also demonstrated significant decrements in mobility. A.L. Hergenroeder, PT, PhD, CCS, Department of Physical Therapy, School of Health and Rehabilitation Sciences, University of Pittsburgh, 6035 Forbes Tower, Pittsburgh, PA 15260 (USA). Address all correspondence to Dr Hergenroeder at: [email protected]. D.M. Wert, PT, MPT, Department of Physical Therapy, School of Health and Rehabilitation Sciences, University of Pittsburgh. E.S. Hile, PT, PhD, NCS, Department of Physical Therapy, School of Health and Rehabilitation Sciences, University of Pittsburgh. S.A. Studenski, MD, MPH, Division of Geriatric Medicine, Department of Medicine, University of Pittsburgh, and VA Pittsburgh Geriatric Research Education and Clinical Center. J.S. Brach, PT, PhD, Department of Physical Therapy, School of Health and Rehabilitation Sciences, University of Pittsburgh. [Hergenroeder AL, Wert DM, Hile ES, et al. Association of body mass index with self-report and performance-based measures of balance and mobility. Phys Ther. 2011;91:1223–1234.] © 2011 American Physical Therapy Association Published Ahead of Print: June 16, 2011 Accepted: April 17, 2011 Submitted: June 25, 2010 Post a Rapid Response to this article at: ptjournal.apta.org August 2011 Volume 91 Number 8 Physical Therapy f 1223 Association of Body Mass Index With Measures of Balance and Mobility O besity is a major public health problem in the United States and around the world. There has been a substantial increase in the prevalence of obesity globally, even in developing countries.1 In the United States, it is estimated that more than 65% of adults are overweight, defined as having a body mass index (BMI) of 25.0 kg/m2 or higher, with more than 30% considered obese (BMIⱖ30 kg/m2). Despite increased attention to this epidemic, the prevalence of obesity continues to rise.2,3 This increasing prevalence is of great concern because the health and economic burdens of obesity are vast. Numerous chronic diseases, including hypertension, cardiovascular disease, type 2 diabetes, osteoarthritis, and certain forms of cancer, are strongly associated with excess body weight.4,5 Obesity is estimated to account for nearly 10% of all medical spending in the United States.6,7 For these reasons, it is imperative that health care professionals be able to effectively evaluate and treat people with conditions related to overweight and obesity. The prevalence of obesity is increasing in older adults, with an estimated 31% of those aged 60 years or older reported to be obese in 2003– 2004.3,8 The increased prevalence of obesity in older adults is especially concerning given the association between obesity and impaired physical function.9 –16 Physical function refers to a person’s ability to perform basic and instrumental activities of daily living and mobility tasks. Impairments in physical function, such as the components of mobility and balance, have been linked to the development of disability.17,18 Analysis of recent trends has shown that obesity-related disability is on the rise,19 reinforcing the need for a better understanding of the impact of obesity on mobility and balance. 1224 f Physical Therapy Volume 91 The BMI is the most common method to quantify weight across a range of body sizes in adults.20 The BMI is calculated by dividing an individual’s weight (in kilograms) by his or her height (in meters squared). Using the BMI, individuals can be classified as underweight (⬍18.5 kg/m2), of normal weight (18.5–24.9 kg/m2), overweight (25– 29.9 kg/m2), class I obese (30 – 34.9 kg/m2), class II obese (35–39.9 kg/m2), or class III obese (ⱖ40 kg/m2). These categories of BMI were developed by the World Health Organization based on associated health risks.21 Guidelines from the National Institutes of Health suggest this anthropometric index should be utilized in the initial assessment of overweight and obesity.22 The BMI is an inexpensive and easyto-use clinical measure that can be administered with minimal training.22 Health care professionals, such as physical therapists, may utilize this simple measure to screen patients and determine risks for diseases associated with obesity. Although BMI is an important indicator of body size for use in the primary care and public health domain, it is an indirect surrogate measure of adiposity and thus has several limitations. The BMI may overestimate body fat in individuals with larger muscle mass, such as athletes, and may underestimate body fat in those who have lost muscle mass (eg, older adults).23 Furthermore, the BMI guidelines were established independent of race, age, and sex. Studies have shown these factors influence the relationship between BMI and percentage of body fat, suggesting the need for population-specific BMI classifications.24,25 For these reasons, it has been suggested that the BMI be used as an initial step in the determination of health risks and that this measure be used in conjunction with waist circumference and assessment Number 8 for the presence of concomitant risk factors.26 The determination of an individual’s BMI may assist the clinician in the identification of risk status and consequently result in an intervention to reduce weight or disease risk. In addition to dietary restriction and behavioral therapy, exercise is a primary treatment for obesity. The public health recommendation for physical activity for adults (men and women who are healthy and 18 – 65 years of age) and older adults (men and women ⱖ65 years of age) is a minimum of 30 minutes of moderateintensity activity on 5 days of the week (150 min/wk).27,28 However, there is evidence that higher levels of exercise are needed for achieving weight loss (150 –250 min/wk) and for maintaining weight loss (⬎250 min/wk).29,30 In older adults with obesity, the benefits of moderate weight loss achieved through diet and exercise include improvements in self-report and performance-based mobility and balance measures.31 In addition, studies have shown that exercise, even in the absence of weight loss, leads to improvement in adverse health consequences associated with obesity.32–34 In view of the widespread prevalence of obesity and the critical role of exercise and physical activity in weight loss and health risk reduction, physical therapists are well positioned to have a substantial impact on this significant public health problem. In a recent study of physical therapists’ knowledge of obesity, the majority believed that identifying obesity was within their scope of practice.35 Furthermore, most therapists recognized that exercise and diet are key components of a weight loss program. Despite these findings, the researchers concluded that physical therapists lacked the knowledge about the use of the BMI as an indicator for identifying obesity August 2011 Association of Body Mass Index With Measures of Balance and Mobility and estimating associated health risks.35 To effectively manage individuals who are overweight, physical therapists must be able to utilize and interpret obesity measures. Despite evidence relating obesity to impaired physical function, there are several limitations in the current body of research. Studies investigating the relationship between BMI and mobility have focused on individuals with severe obesity,36,37 and few studies have examined the relationship between BMI and balance.38 Thus, little is known about the impact of BMI on balance and mobility across the broader continuum of weight ranges. This information would enable health care professionals to better estimate the functional consequences of excess weight. Furthermore, it is not known how commonly used clinical measures of mobility and balance are affected by BMI. This knowledge would assist physical therapists in determining whether it is necessary to alter tests and measures for patients who are obese. The purposes of this study were: (1) to assess differences in mobility and balance on self-report and performance-based measures across the spectrum of weight categories, (2) to describe how mobility and balance measures are affected by BMI, and (3) to examine other factors that might explain the association between BMI and mobility and balance. Method Participants This cross-sectional study examined older adults who participated in the baseline data collection of an ongoing observational study at the Claude D. Pepper Older Americans Independence Center, Pittsburgh, Pennsylvania (N⫽120). Individuals were recruited from a research registry of older adults who previously consented to be contacted for studies of balance and mobility. Participants August 2011 were included in the study if they were 65 years of age or older and had the ability to walk a minimum of a household distance with or without an assistive device and without the assistance of another person. Participants were excluded if they had any of the following conditions that might affect their safety during testing: neuromuscular disorders that impair movement, cancer with active treatment, hospitalization for a life-threatening illness or major surgery in the previous 6 months, severe pulmonary disease, chest pain with activity, or a cardiac event such as a heart attack in the previous 6 months. Body mass index data were missing on one individual; thus, 119 participants were included in the data analysis. Body Mass Index Height and weight were measured using a Tanita BWB-800 scale and HR-200 wall-mounted height rod.* Participants were measured while wearing indoor clothing and socks without shoes. Assistance was given to obtain the position for both height and weight measurements, including cues to stand up straight with heels against the wall for assessment of height, but measurements then were recorded in unsupported stance. Weight was recorded to the nearest tenth of a kilogram, and height was measured to the nearest tenth of a centimeter with the height rod at the top of the participant’s head in midline. Height and weight measurements were used to determine BMI. The BMI classifications used in this study were based on the World Health Organization’s definitions of normal weight (BMI 18.5 to ⬍25 kg/m2), overweight (BMIⱖ25 to ⬍30 kg/m2), class I obesity (BMIⱖ30 to ⬍35 kg/m2), class II obesity (BMIⱖ35 to ⬍40 kg/m2), and class * Tanita Corporation of America Inc, 2625 S Clearbrook Dr, Arlington Heights, IL 60005. III obesity (BMIⱖ40 kg/m2). Because of the limited number of participants with class III obesity (n⫽3), participants in the obese categories were classified based on obesity severity into moderately obese (BMIⱖ30 to ⬍35 kg/m2) and severely obese (BMIⱖ35 kg/m2) weight groups.39,40 Self-Report Measures of Mobility and Balance A 5-point Likert scale was used to obtain a global rating of mobility and balance for each participant. Participants were asked to rate their current level of mobility and balance as excellent, very good, good, fair, or poor. Self-report measurements of balance and mobility were collected prior to the performance-based measures so that the participants’ performance on the tests would not influence their self-report. Performance-Based Measures of Mobility Figure-of-8 Walk Test. The Figure-of-8 Walk Test (F8W) has been shown to be a valid measure of walking skill in older adults based on correlations with gait speed, measures of physical function (Late Life Function and Disability Instrument), and activities of daily living (Physical Performance Test).41 In a study of older adults, the interrater reliability of this measure was determined to be high (intraclass correlation coefficient [ICC]⫽.85–.92).42 Participants were asked to walk in a figure-of-8 pattern around 2 cones placed 1.524 m (5 ft) apart on the floor. The number of steps taken to complete the course and the total elapsed time in seconds were measured. Gait speed. Gait speed is a valid measure to predict health-related outcomes in older adults, including falls and disability.43,44 Studies of older adults who were healthy and those with disease have shown the test-retest reliability of this measure to be high (ICC⬎.90).43– 45 Volume 91 Number 8 Physical Therapy f 1225 Association of Body Mass Index With Measures of Balance and Mobility The GaitMat II system† was used to measure gait speed.46 The GaitMat II consists of an approximately 4-mlong, pressure-sensitive walkway controlled by a computer system that processes the data to generate both spatial and temporal variables of walking. On either end of the 4-mlong active walkway, nearly 2 m of inactive surface was available so that acceleration and deceleration were not captured in the timed walk. Gait speed was determined by dividing the distance traversed by the time between the first and last steps (eg, switch closure) and was recorded in meters per second. After 2 practice passes, each participant completed 4 passes at his or her self-selected walking speed for data collection. The mean of the 4 passes was used as the measure of gait speed. Timed “Up & Go” Test. The Timed “Up & Go” Test has been used as a test of basic mobility in older adults and has been shown to have high intrarater and interrater reliability (ICC⬎.90).47,48 For this test, the time required for each participant to stand up from a chair, walk 3 m, turn, walk back, and sit down was measured and recorded. Six-Minute Walk Test. The 6Minute Walk Test has been used as a measure of mobility and aerobic endurance in older adults with and without disease and has shown to be a reliable measure (ICC⬎.90).49 Each participant was asked to walk as far as possible in 6 minutes, taking standing rest periods as needed. A straight path of 15.24 m (50 ft) was used. The total distance walked back and forth in 6 minutes was recorded. Each participant’s heart rate, blood pressure, rating of perceived exertion, and signs and symptoms were monitored before and after testing. † E.Q. Inc, PO Box 16, Chalfont, PA 189140016. 1226 f Physical Therapy Volume 91 Timed chair stands. Chair stands have been utilized as a performancebased measure of lower body function and have been shown to have good reliability in older adults (ICC⬎.80).50 Participants were seated in a rigid chair, asked to fold their arms across their chest, and stand up straight as quickly as possible 5 times. The time to complete 5 repeated stands from the chair was recorded. Performance-Based Measures of Balance Timed balance measures. Participants were asked to maintain their balance for up to 30 seconds under each of the following conditions: standing with eyes closed while the feet were positioned as close together as possible, tandem stance in which the heel of one foot was directly in front of and touching the toes of the other foot, and singleleg stance where the participants were asked to lift one foot off the ground and maintain their balance on the remaining leg. The first 2 tests are a modification of standard balance tests used in the Established Populations for Epidemiologic Studies of the Elderly (EPESE) project.51 In the current study, times for each trial were extended from 10 to 30 seconds, and no support was provided to attain the test position. Interrater reliability (ICC⬎.9) and test-retest reliability (ICC⫽.7) have been demonstrated for the EPESE battery of tests.52 In a previous study of older adults who were high functioning, change of the reliability coefficient of single-leg stance was shown to be .69.50 Postural responses. The postural stress test was used to test postural responses to a destabilizing force applied manually by an examiner in 3 different directions (posteriorly, right, and left). Previous research has shown that older adults classified as “fallers” score lower on postural Number 8 response tests compared with older “nonfallers” and young adults.53 The ability of the participants to remain upright and their response when nudged at the pelvis in various directions were graded. The response was graded using the following scale: 0⫽responds (single step); 1⫽ responds (multiple steps); 2⫽ responds but requires support to stabilize; and 3⫽no obvious response, individual must be supported. The responses to 6 perturbations, 2 in each of the 3 directions, were totaled, with higher scores indicating greater impairment. Narrow walk test. As previously described by Bandinelli et al,54 participants were asked to walk a distance of 4 m at their usual walking pace within a 15-cm-wide path marked on the floor with tape. The time taken to complete the task was recorded. The number of deviations from the 15-cm-wide path was also recorded. Individuals who could not complete the test independently, or who stepped outside the walkway more than 10 times, were classified as “unable.” The test-retest reliability of this measure (ICC⫽.76) has been demonstrated in a sample of older adults.54 Concurrent validity of the narrow walk test has been established based on moderate to strong correlations with other measures of physical performance, such as gait speed and the 400-m corridor walk, in a sample of older adults.55 Obstacle walk test. As previously described by Bandinelli et al,54 participants were asked to walk a 7-m course at their usual walking pace and step over 2 obstacles of different heights. One obstacle was 6 cm tall and positioned 2 m from the starting line, and the other obstacle was 30 cm tall and positioned 4 m from the starting line. The time taken to complete this task was recorded. The obstacle walk test has shown to be a August 2011 Association of Body Mass Index With Measures of Balance and Mobility Table 1. Participant Demographics Stratified by Weight Groupa Normal Weight (BMIⴝ18.5–24.9 kg/m2) (nⴝ28) Overweight (BMIⴝ25–29.9 kg/m2) (nⴝ43) Moderate Obesity (BMIⴝ30–34.9 kg/m2) (nⴝ31) Severe Obesity (BMI>35 kg/m2) (nⴝ17) P BMI (kg/m2), X (SD) 22.9 (1.5) 27.6 (1.6) 31.8 (1.6) 38.2 (2.1) ⬍.001 Age (y), X (SD) 77.0 (6.3) 78.1 (5.5) 78.0 (6.4) 76.0 (5.8) .58 Variable Demographic characteristics Sex , % female 75% 64% 71% 88% .31 100% 90% 81% 76% .05 82% 64% 68% 59% .06 76% 62% 58% 31% .03 Reported fear of falling 36% 42% 45% 56% .60 Reported fall in previous year 32% 41% 41% 38% .86 White College educated Activity level Walk for exercise Fall characteristics Comorbid conditions, X (SD) 4.3 (1.9) 4.0 (2.0) 4.9 (2.1) 4.9 (1.9) .19 Angina 11% 10% 13% 12% .98 Heart attack 11% 5% 10% 12% .73 0% 2% 12% 6% .11 Lung disorders 19% 14% 48% 18% .005 Arthritis 70% 69% 81% 88% .35 Osteoporosis 48% 29% 23% 24% .15 7% 10% 29% 12% .06 Congestive heart failure Diabetes Chronic pain a 0% 2% 10% 6% .27 Sleep problems 11% 19% 13% 29% .39 Cancer 33% 26% 29% 41% .70 Stroke 4% 5% 10% 18% .30 BMI⫽body mass index. reliable measure (ICC⫽.89) in older adults.54 Three licensed physical therapists and one research assistant with extensive experience in geriatric research were responsible for data collection, including measurement of height and weight, as well as administration of the battery of balance and mobility tests. All testers received training in conducting the measurements and were blinded to the purposes of the study but not to study outcomes. Participants’ BMIs were calculated after data collection was completed. August 2011 Additional Information Demographics. Data were collected on the following demographic factors: age, sex, ethnicity, and education level. Comorbidities Index. This measure is a self-report of common physician-diagnosed medical conditions, including cardiovascular disease (angina, congestive heart failure, or heart attack), neurologic conditions (stroke or Parkinson disease), lung disease, musculoskeletal conditions (arthritis, osteoporosis, fracture, or joint replacement), general conditions (depression, sleep problems, or chronic pain syn- drome), cancer, diabetes, or visual conditions (glaucoma or cataracts).56 For each medical condition, participants were asked whether they had ever been told by a physician that they had the condition. The number of affirmative responses was summed to yield a total score. Fall history questionnaire. Participants were asked to respond to the following questions: (1) Are you afraid of falling? and (2) Have you had a fall in the previous year? Responses to the questions were recorded as “yes” or “no.” Volume 91 Number 8 Physical Therapy f 1227 Association of Body Mass Index With Measures of Balance and Mobility Figure. Global rating of mobility and balance as excellent or very good, stratified by weight group. Asterisk indicates P⫽.005. Physical activity habits. During administration of the Survey of Activities and Fear of Falling in the Elderly,57 participants were asked whether they currently walk for exercise. Because walking is the most common form of exercise for older adults,58 those who responded affirmatively to the question were considered to be more physically active than those who responded negatively. Data Analysis Individuals were classified as being of normal weight, overweight, moderately obese, or severely obese based on their BMI. For continuous data, descriptive statistics are presented as means and standard deviations, and categorical data are presented as frequencies (percentages). Mobility and balance were compared among weight groups using analysis of variance (ANOVA). Post hoc pairwise comparisons were conducted for continuous data. Chi-square analyses were conducted for categorical data. One-tailed tests were used because there was a directional hypothesis that mobility and balance would be poorer as BMI increased. 1228 f Physical Therapy Volume 91 Multiple linear regression analysis was used to examine the association between BMI and mobility and balance during standing and walking while controlling for age, sex, minority status, education level, physical activity level, and number of comorbid conditions. The level of significance was set at .05. Data analyses were performed with the SAS statistical package (version 9.2).‡ Role of the Funding Source This research was funded by The University of Pittsburgh Older Americans Independence Center (grant P30 AG024827). Dr Brach was supported by a Paul B. Beeson Career Development Award (K23 AG026766). Dr Studenski was supported by the National Institute on Aging (grant K07 AG023641). Results Table 1 provides a summary of the demographic variables, behavioral risk factors, fall characteristics, and ‡ SAS Institute Inc, 100 SAS Campus Dr, Cary, NC 27513-2414. Number 8 prevalent chronic conditions for all participants stratified by weight group. Of the 119 participants, 28 (24%) were of normal weight (BMI⫽18.5–24.9 kg/m2), 43 (36%) were overweight (BMI⫽25–29.9 kg/m2), 31 (26%) were moderately obese (BMI⫽30 –34.9 kg/m2), and 17 (14%) were severely obese (BMIⱖ35 kg/m2). The mean age of the participants was 77.6 years (SD⫽5.9). There were more women (72%) in our sample than men, and most participants classified their race as white (87%). Several characteristics of the participants were associated with higher BMI levels. Individuals with higher BMI levels were more likely to be black or Hispanic and less likely to report walking for exercise compared with the normal weight group (Pⱕ.05). There were no differences among weight groups in the total number of comorbid health conditions reported. However, compared with the other weight groups, those who were moderately obese were more likely to report having lung disorders (P⫽.005). There were no differences in the number of falls or fear of falling among weight groups. The Figure illustrates self-reported global mobility and balance ratings stratified by weight group. Compared with participants who were of normal weight and those who were overweight, those with moderate and severe obesity were less likely to report their mobility as very good or excellent (52%, 55%, 39%, and 6%, respectively; P⫽.005). There were no differences in self-reported ratings of balance among weight groups. Table 2 provides a description of performance-based mobility and balance measures stratified by weight group. Participants with severe obesity (n⫽17) had the lowest levels of mobility on the performance-based measures, followed by those who August 2011 Association of Body Mass Index With Measures of Balance and Mobility Table 2. Description of Performance-Based Mobility and Balance Measures Stratified by Weight Group Normal Weight (nⴝ29) X (SD) Measure Overweight (nⴝ42) X (SD) Moderate Obesity (nⴝ31) X (SD) Severe Obesity (nⴝ17) X (SD) P Mobility Figure-of-8 walk test (s) Gait speed (m/s) 9.1 (2.8) 9.3 (2.6) 11.2 (4.5) 11.4 (4.5) .02 1.20 (0.2) 1.11 (0.2) 1.0 (0.3) 0.86 (0.2) ⬍.001a 9.1 (3.2) 9.9 (2.6) 11.7 (4.5) 12.9 (4.9) .002b Timed “Up & Go” Test (s) 1,278.3 (276.2) 1,184.9 (266.7) 954.1 (282.5) 836.9 (389.9) ⬍.001d 12.2 (2.7) 13.8 (4.0) 15.3 (5.4) 15.9 (6.3) .03 Eyes closed, narrow stance (s) 29.2 (2.8) 29.3 (4.2) 26.2 (8.4) 28.4 (6.6) .12 Tandem stance test (s) (n⫽89) 22.4 (11.4) 21.3 (11.0) 21.7 (11.3) 19.4 (12.9) .89 Unilateral stance test (s) (n⫽97) 10.6 (9.7) 10.1 (8.8) 6.2 (7.0) 6.4 (7.9) .17 3.4 (2.9) 3.5 (4.1) 3.2 (2.3) 3.6 (3.3) .96 Narrow walk test (s) (n⫽101) 4.9 (1.6) 5.3 (2.4) 5.8 (1.9) 5.7 (1.5) .32 Narrow walk test (no. of deviations) 1.3 (2.5) 2.5 (3.8) 2.5 (2.9) 3.8 (2.9) .14 Obstacle walk test (s) 8.0 (4.5) 8.2 (3.5) 10.7 (7.8) 10.8 (4.5) .10 Six-Minute Walk Test (ft)c (n⫽107) Timed chair stands (s) (n⫽105) Balance with standing Postural responses (total no.) Balance with walking a Difference between normal weight and moderate obesity⫽0.21 s, 95% confidence interval (CI)⫽0.03– 0.38, P⬍.05; difference between normal weight and severe obesity⫽0.34 s, 95% CI⫽0.13– 0.54, P⬍.05. b Difference between normal weight and severe obesity⫽3.82 s, 95% CI⫽0.65–7.0, P⬍.05; difference between overweight and severe obesity⫽3.02 s, 95% CI⫽0.03– 6.01, P⬍.05. c 1 ft⫽0.3048 m. d Difference between normal weight and moderate obesity⫽324 ft, 95% CI⫽96 –553, P⬍.05; difference between normal weight and severe obesity⫽441 ft, 95% CI⫽174 –709, P⬍.05; difference between overweight and moderate obesity⫽231 ft, 95% CI⫽20 – 441, P⬍.05; difference between overweight and severe obesity⫽348 ft, 95% CI⫽95– 601, P⬍.05. were moderately obese (n⫽31), overweight (n⫽42), and of normal weight (n⫽29). Higher BMI category was not associated with differences in balance. For the mobility measures, post hoc pair-wise comparisons revealed that individuals who were of normal weight and those who were overweight were similar in performance; however, individuals with obesity performed more poorly compared with the other weight groups. Table 3 provides the results for the percentage of participants who were able to complete the performancebased measures of balance. Compared with those who were overweight and those who were of normal weight, a trend was observed with a greater percentage of partici- Table 3. Percentage of Completion for Performance-Based Measures of Balance by Weight Group Normal Weight Overweight Moderate Obesity Severe Obesity P Tandem stance test 79% 79% 65% 76% .42 Unilateral stance test 90% 86% 77% 64% .10 Narrow walk test 83% 93% 81% 76% .48 Obstacle walk test 90% 95% 90% 82% .60 Measure August 2011 pants with moderate and severe obesity unable to complete the unilateral stance test (P⫽.10). Table 4 provides the results for the series of linear regressions examining the association between BMI and mobility and between BMI and balance during standing and walking. In unadjusted analyses (model 1), BMI was most strongly related to mobility (gait speed, adjusted R2⫽ .14, P⬍.0001) and to a lesser extent related to balance during standing (unilateral stance test, adjusted R2⫽ .04. P⬍.03) and balance during walking (obstacle walk test, adjusted R2⫽.03, P⬍.04). After adjusting for age, sex, minority status, physical activity level, and total number of comorbid conditions (model 2), BMI remained significantly related to Volume 91 Number 8 Physical Therapy f 1229 Association of Body Mass Index With Measures of Balance and Mobility Table 4. Relationship Between Body Mass Index (BMI) and Mobility and Between BMI and Balance During Standing and Walking Gait Speed Measure BMI,  (SE)c Adjusted R2 Model P value a Unilateral Stance Test b Model 1 Model 2 ⫺0.02 (0.004)d ⫺0.015 (0.004)d .14 .41 ⬍.0001 ⬍.0001 Obstacle Walk Test Model 1 Model 2 Model 1 Model 2 ⫺0.39 (0.173)e ⫺0.33 (0.189) 0.20 (0.099)e 0.18 (0.093) .04 ⬍.03 .13 ⬍.004 .03 ⬍.04 .20 ⬍.0001 a Unadjusted linear regression. Linear regressions adjusted for age, sex, minority status, education level, physical activity level, and total number of comorbid conditions. SE⫽standard error. d P⬍.001. e P⬍.05. b c mobility (⫽⫺.015, standard error [SE]⫽.004, P⬍.0001). Body mass index approached having a significant association with balance during standing (⫽⫺.331, SE⫽.189, P⬍.08) and balance during walking (⫽.181, SE⫽.093, P⬍ .06). Discussion When examining balance and mobility across weight groups in community-dwelling older adults, there were more differences in mobility than in balance. Individuals who were classified as being of normal weight and those classified as overweight were similar in mobility, but individuals with moderate obesity and those with severe obesity demonstrated consistently lower performance than the other groups. The observed relationship between BMI and poor mobility suggests that mobility in older adults is impaired at all levels of obesity. In our study, self-report of mobility, but not balance, was different for participants with obesity. Individuals who were of normal weight and those who were overweight had a similar perception of mobility. Although self-reported mobility declined for participants who were moderately obese, those with more severe obesity were much less likely to report mobility as very good or excellent. The finding of more frequent self-reported mobility limita1230 f Physical Therapy Volume 91 tion in individuals with obesity is consistent with the findings of previous studies in older adults.10,14,59 In a study of 6,981 older men and women, LaCroix et al14 found that there was a strong association between loss of mobility and high BMI levels. Launer et al10 examined the association between BMI and self-reported mobility disability in the NHANES I Epidemiological Follow-up Study and found that BMI was related to mobility disability in community-dwelling older women; specifically, individuals in the high tertile for BMI had greater risk of impairment compared with those in the low tertile for BMI. Higher BMI levels were associated with poorer mobility on performancebased measures. Thus, our participants’ self-reports of poor mobility were consistent with the findings on the performance-based measures. We found that mobility worsened with increased BMI level; however, post hoc pair-wise comparisons revealed the groups with moderate and severe obesity differed from the other weight groups on most of the measures. In our sample, only the normal weight group achieved a desirable gait speed (ⱖ1.2 m/s) based on a previous study in older adults.60 For participants who were overweight and those who were obese, the Number 8 mean gait speed was ⬍1.2 m/s, which may have implications for these individuals to function successfully in the community. For example, in order to safely negotiate through a traffic intersection, an individual must be able to walk at a speed of 1.2 m/s.61 Furthermore, the gait speeds found in the participants classified as moderately or severely obese (1.0 and 0.86 m/s) are not just indicative of impaired functioning, but also have been found to be associated with higher risk for adverse health events, including nursing home admission, falls, and disability.60,62 These findings underscore the detrimental impact that excess weight has on mobility in older adults, even in those with less severe obesity. Higher BMI levels were not associated with poorer performance on measures of balance during standing, which is consistent with participants’ self-reported balance. This finding was not surprising given that there were no differences in fall history among the weight groups; however, our findings differ from those of previous studies that demonstrated more postural instability38 and greater risk of falls in individuals with obesity.63 Although increased BMI in older adults may influence balance, other factors associated with aging also may contribute to postural instability. These factors include sarcopenia, defined as the August 2011 Association of Body Mass Index With Measures of Balance and Mobility age-related loss of skeletal muscle mass and strength (force-generating capacity)64; changes in body fat distribution, specifically an increase in visceral abdominal fat and a decrease in subcutaneous fat65; and a decline in the quality of skeletal muscle.66 It is plausible that changes in skeletal muscle and body fat distribution may be related more to postural instability than to BMI alone, which may explain the lack of a stronger relationship between balance and BMI in the current study. Although not statistically significant, differences in static balance among weight groups may be clinical meaningful. For example, individuals who were of normal weight and those who were overweight had similar performance on the unilateral stance test (10.6 and 10.1 seconds, respectively) compared with individuals with moderate obesity and those with severe obesity, who had poorer performance on the unilateral stance test (6.2 and 6.4 seconds, respectively). A previous study of falls in older adults who were obese showed no difference in performance on standing balance tests in individuals with obesity compared with those of normal weight; however, in contrast to our study, individuals with obesity reported a higher prevalence of falls.63 Interestingly, all measures of balance were static, and no measures of balance during walking were included. Further investigation of the impact of obesity on balance in older adults is warranted and should take into account skeletal muscle mass, strength, and body fat distribution. A greater number of individuals with moderate obesity and severe obesity were unable to complete the performance-based measures of balance compared with those who were of normal weight and those who were overweight. Lack of completion of balance measures in parAugust 2011 ticipants with higher BMI was related to inability to assume the test positions (eg, tandem stance) and difficulty performing certain movements (eg, narrow walk test). Thus, had all participants with obesity been able to complete the balance measures, our results may have differed. These findings reinforce the need for the identification of balance measures most appropriate for use in individuals with higher BMIs, specifically those that incorporate balance during dynamic activities and those that allow individuals with differing body sizes to assume the position required for the test. Obesity is associated with increased burden of chronic disease and decreased physical activity level, both of which have been shown to negatively affect mobility.14,67,68 In the current study, individuals with obesity were more likely to have lung disorders and were less likely to engage in physical activity compared with those who were overweight and those of normal weight. The association between BMI and mobility was partially explained by these factors; however, the data suggest that even after adjusting for many potential confounding factors, BMI still was independently related to mobility. The recommendation for weight loss in older adults is controversial because there is a risk of accelerating the age-related decline in lean mass and bone density, thereby leading to poorer physical function.69,70 However, interventions that facilitate weight loss through diet and exercise have been shown to improve mobility, balance, and health-related quality of life in older adults.31,71–73 Villareal et al8 suggested that weight loss programs for older adults include strategies to minimize muscle and bone loss and should include the adoption of resistance exercise and regular physical activity. This recommendation should be taken into account by physical therapists who are frequently involved in exercise prescription for older adults with obesity. There are several limitations to the current study. First, the results of the study may not apply to the general community-dwelling older population because our sample was a volunteer sample of predominantly white women. Furthermore, there were unequal numbers of participants in each weight group, and not all participants were able to complete the physical performance tests. Individuals in the moderately and severely obese categories had the lowest completion rates compared with those in the normal weight or overweight categories. Our results might have differed had there been equal numbers of participants in the weight groups and had completion rates been higher across the weight groups. Several testers were responsible for data collection in this study, which could have influenced the differences among the weight groups. However, we believe this potential limitation is unlikely in that participant assignment to testers was completely random and all testers evaluated participants from each of the BMI groupings. In addition, although not established in our study, the interrater reliability of many of the measures that we used has been established in other studies and is quite good. An additional limitation of the current study was the use of the BMI as an indicator of body size. Older individuals typically have less lean mass and more fat mass than younger adults, and as a result, the BMI may underestimate body fat in these individuals.74 Furthermore, there is debate about whether the fat redistribution and relative loss of fat-free mass that occur with aging may exert more influence than the BMI in Volume 91 Number 8 Physical Therapy f 1231 Association of Body Mass Index With Measures of Balance and Mobility determining health risks associated with obesity in older adults.75 More sophisticated measures of total body fat are available, including dualenergy x-ray absorptiometry (DXA) and electron beam computed tomography (EBT). Even so, prior research has shown a strong relationship between BMI and total body fat determined by EBT in older women (r⫽.89, P⬍.0001), suggesting that BMI may be an acceptable initial screening tool in the clinical setting.76 In addition, DXA and EBT may not be practical measures of total body fat in the clinical setting because these tests are more timeconsuming, require more complex training, and are expensive to use. We recognize the limitations of the BMI; however, in the absence of a more suitable measure, the use of the BMI may provide an opportunity for physical therapists to incorporate health promotion into clinical practice. When utilizing the BMI, care should be taken to interpret results along with assessment of regional fat distribution as well as visual inspection of fat and muscle mass to decrease risk of misclassification of body size. Conclusion This study used a comprehensive battery of self-report and performance-based measures to characterize mobility and balance in older adults who were of normal weight, overweight, moderately obese, and severely obese. Higher BMI levels were associated with poorer mobility but not balance. Furthermore, individuals classified as being of normal weight and those classified as overweight were similar in mobility, whereas individuals with obesity had greater impairments in mobility. Although those participants with severe obesity (BMIⱖ35 kg/m2) were most impaired, older adults with less severe obesity (BMI⫽30 –34.9 kg/m2) also demonstrated significant decrements in 1232 f Physical Therapy Volume 91 mobility. Body mass index should be considered when selecting measures of mobility and balance because older adults with obesity may be unable to achieve the position for some tests. When treating older adults with obesity, physical therapists are in a unique position to prescribe exercise to address associated medical complications as well as the functional consequences of obesity. Dr Hergenroeder and Dr Brach provided concept/idea/research design and data analysis. All authors provided writing. Mr Wert, Dr Hile, and Dr Brach provided project management. Dr Studenski and Dr Brach provided fund procurement and facilities/equipment. Dr Brach provided participants. Mr Wert and Dr Studenski provided consultation (including review of manuscript before submission). This study was approved by the Institutional Review Board of the University of Pittsburgh. This work was presented on at Physical Therapy 2009: APTA’s Annual Conference & Exposition; June 12, 2009; Baltimore, Maryland. This research was funded by The University of Pittsburgh Older Americans Independence Center (grant P30 AG024827). Dr Brach was supported by a Paul B. 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J Gerontol A Biol Sci Med Sci. 2003;58:1012–1017. 70 Jensen LB, Quaade F, Sorensen OH. Bone loss accompanying voluntary weight loss in obese humans. J Bone Miner Res. 1994; 9:459 – 463. 1234 f Physical Therapy Volume 91 71 Messier SP, Loeser RF, Mitchell MN, et al. Exercise and weight loss in obese older adults with knee osteoarthritis: a preliminary study. J Am Geriatr Soc. 2000;48: 1062–1072. 72 Christensen R, Bartels EM, Astrup A, Bliddal H. Effect of weight reduction in obese patients diagnosed with knee osteoarthritis: a systematic review and meta-analysis. Ann Rheum Dis. 2007;66:433– 439. 73 Messier SP, Loeser RF, Miller GD, et al. Exercise and dietary weight loss in overweight and obese older adults with knee osteoarthritis: the Arthritis, Diet, and Activity Promotion Trial. Arthritis Rheum. 2004;50:1501–1510. Number 8 74 Borkan GA, Hults DE, Gerzof SG, et al. Age changes in body composition revealed by computed tomography. J Gerontol. 1983; 38:673– 677. 75 Zamboni M, Mazzali G, Zoico E, et al. Health consequences of obesity in the elderly: a review of four unresolved questions. Int J Obes (Lond). 2005;29:1011– 1029. 76 Storti KL, Brach JS, FitzGerald SJ, et al. Relationships among body composition measures in community-dwelling older women. Obesity (Silver Spring). 2006; 14:244 –251. August 2011 Research Report Frontal-Plane Gait Mechanics in People With Medial Knee Osteoarthritis Are Different From Those in People With Lateral Knee Osteoarthritis Robert J. Butler, Joaquin A. Barrios, Todd Royer, Irene S. Davis Background. The majority of research on gait mechanics in knee osteoarthritis has focused on people with medial compartment involvement. As a result, little is known about the gait mechanics of people with the less common, lateral compartment disease. Objective. The objective of this study was to compare walking mechanics— R.J. Butler, PT, DPT, PhD, Doctor of Physical Therapy Division, Department of Community Health and Family Medicine, Duke University, DUMC 104002, Durham, NC 27705 (USA). Address all correspondence to Dr Butler at: [email protected]. specifically, differences in frontal-plane lower-extremity kinematics and kinetics—in people with medial knee osteoarthritis, people with lateral knee osteoarthritis, and people who were healthy. J.A. Barrios, PT, DPT, PhD, Doctor of Physical Therapy Program, University of Dayton, Dayton, Ohio. Design. A cross-sectional design was used. T. Royer, PhD, Department of Kinesiology and Applied Physiology, University of Delaware, Newark, Delaware. Methods. Fifteen people with medial knee osteoarthritis, 15 people with lateral knee osteoarthritis, and 15 people who were healthy (control group) were recruited for the study. All participants underwent a gait analysis at an intentional walking speed. The variables of interest for the study were peak frontal-plane moments and angles and angular excursions of the lower extremity during the stance phase of gait. Data were statistically analyzed with a one-way analysis of variance. Results. Participants with lateral knee osteoarthritis exhibited significantly less knee adduction excursion, lower peak knee abduction moment, and lower peak rear-foot eversion compared with the control group and the medial knee osteoarthritis group. Limitations. Participants in the control group were approximately 10 years younger than participants with knee osteoarthritis. Despite this difference, neither body mass index nor gait speed, each of which is a factor with a stronger influence on gait mechanics, differed among the groups. Conclusions. Participants with lateral knee osteoarthritis exhibited frontal-plane gait mechanics at the knee and rear foot that were different from those of participants with medial knee osteoarthritis. The results of this study may guide the development of interventions specific to treating people with lateral knee osteoarthritis. I.S. Davis, PT, PhD, Department of Physical Therapy, University of Delaware, and Drayer Physical Therapy Institute, Hummelstown, Pennsylvania. [Butler RJ, Barrios JA, Royer T, Davis IS. Frontal-plane gait mechanics in people with medial knee osteoarthritis are different from those in people with lateral knee osteoarthritis. Phys Ther. 2011;91:1235–1243.] © 2011 American Physical Therapy Association Published Ahead of Print: June 16, 2011 Accepted: March 21, 2011 Submitted: September 27, 2010 Post a Rapid Response to this article at: ptjournal.apta.org August 2011 Volume 91 Number 8 Physical Therapy f 1235 Frontal-Plane Gait Mechanics in Knee Osteoarthritis K nee osteoarthritis (OA) is a degenerative joint disease characterized by pain and stiffness.1 These symptoms are related to disruption of the articular surfaces and are associated with significant impairment in functional ability.2 The disease prevalence increases with age, and currently 12% to 16% of people older than 65 years of age in the United States have been diagnosed with knee OA.3,4 It has been estimated that almost 45% of all people in the United States will develop knee OA during their lifetime.5 With the growing prevalence of the disease, a concomitant growth in the cost of treating the disease also has been observed. The cost for endstage treatment of the disease has been estimated to be $38,000.6 Projections show that the cost will continue to rise as the baby boomer generation enters the age range for typical symptomatic disease presentation. Tibiofemoral knee OA can develop in either the medial or lateral compartment.7 However, it is 9 times more common in the medial compartment.7 Static lower-extremity alignment has been shown to influence which compartment is involved, with genu valgus being associated with lateral OA and genu varus being associated with medial OA.8 –11 Genu valgus alignment often is associated with hip adduction proximally and rear-foot eversion distally.12 Genu varus alignment, however, is associated with decreased hip adduction proximally and increased rear-foot inversion distally. To date, only one study has compared the gait mechanics of people who have medial knee OA with those of people who have lateral knee OA.13 These researchers reported that, relative to people in a control group, people with medial knee OA exhibited more knee 1236 f Physical Therapy Volume 91 adduction but less hip adduction during gait than people with lateral knee OA.13 Alterations in hip and knee alignment are likely to lead to differences in respective joint loading. Weidow et al13 noted that people with medial knee OA had 52% higher internal knee abduction moments than people who were healthy (control group). People with lateral knee OA had 63% lower internal knee abduction moments than the control group.13 Surprisingly, lower internal peak hip abduction moments were reported in both people with medial knee OA and people with lateral knee OA than in the control group. Mundermann et al14 observed similar reductions in hip abduction moments in people with severe medial knee OA and in the control group. However, they found no difference between people with less severe medial knee OA and the control group. Alterations at the hip and knee are likely to influence mechanics distally and thus can significantly alter gait mechanics. Unfortunately, previous research studies did not include an evaluation of the differences in these distal mechanics, such as peak rear-foot eversion, eversion excursion, and the peak inversion moment. In summary, knee OA is clearly associated with some malalignment of the lower extremity. The direction of knee malalignment (varus or valgus) influences which knee compartment becomes involved and likely influences gait mechanics. However, only one study has compared the gait mechanics of people who have been diagnosed with medial knee OA and those of people who have been diagnosed with lateral knee OA. In addition, no studies have examined the effect of these differences on rearfoot mechanics during gait. Therefore, the purpose of this study was to compare frontal-plane gait mechanics at the hip, knee, and rear foot in people with medial knee OA, people with lateral knee OA, and people who were healthy (control group). The Bottom Line What do we already know about this topic? Patients with medial and lateral knee osteoarthritis exhibit different hip and knee mechanics during gait. These differences in mechanics have previously been associated with elevated disease progression. What new information does this study offer? The findings from this study suggest that patients with medial and lateral knee osteoarthritis also have different mechanics at the ankle. The observed differences in mechanics are contrary to current clinical beliefs. The difference in presentation may be due to the chronic effects of the disease process. If you’re a patient, what might these findings mean for you? If you have osteoarthritis on the inside of the knee (medial knee osteoarthritis), the treatments you receive may be different from the treatments that patients with knee osteoarthritis on the outside of the knee (lateral knee osteoarthritis) may receive. Number 8 August 2011 Frontal-Plane Gait Mechanics in Knee Osteoarthritis We hypothesized that, compared with people with lateral knee OA or the control group, people with medial knee OA would walk with increased peak knee adduction, increased knee adduction excursion, and an increased peak internal knee abduction moment. We also hypothesized that, compared with people with lateral knee OA or the control group, people with medial knee OA would exhibit decreased hip adduction, decreased hip adduction excursion, and a decreased peak hip abduction moment. Finally, we expected that people with lateral knee OA would exhibit increased rear-foot eversion, increased eversion excursion, and an increased peak inversion moment and that, for all variables of interest, values in the control group would fall between values in people with medial knee OA and values in people with lateral knee OA. Method We conducted an a priori power assessment for a one-way analysis of variance (ANOVA) design for the variables peak knee adduction and peak knee abduction moment. Using a  value of .20, an ␣ value of .05, a difference between groups of 10%, and the variability from previously published work, we determined that 14 people per group were needed to adequately power the study.15,16 Therefore, 15 people per group were recruited through local advertisements. Participants All participants were 40 to 75 years of age. The participants in the control group were asymptomatic and had no history of knee problems. The participants with OA were diagnosed with unilateral medial or lateral compartment tibiofemoral OA on the basis of a flexed-knee radiograph that was graded by a single rheumatologist. People were excluded if they had any other August 2011 lower-extremity arthritis. A KellgrenLawrence (K-L) grade was assigned to each radiograph to classify disease severity.17 A K-L grade of 2 or higher was required for inclusion in the study. In addition, all participants with OA had to report knee pain of at least 3 of 10 on a verbal analog scale during walking activities to be included in the study. Exclusion criteria included any other pathological condition that could affect ambulation. People with evidence of symptomatic, patellofemoral compartment involvement were excluded. Finally, all participants had to be able to ambulate without an assistive device. Study Design People who met the inclusion criteria were invited to a motion analysis laboratory for an instrumented gait analysis. Participants first provided written informed consent. Next, anatomical markers were placed over the following landmarks on the limb that was diagnosed with knee OA: the greater trochanters, the medial and lateral femoral condyles, the medial and lateral malleoli, the heads of the first and fifth metatarsals, and the distal aspect of the laboratory shoe (Nike Air Pegasus*). Tracking markers were placed on the skin over the L5–S1 interspinous space, the ipsilateral anterior superior iliac spine, and the ipsilateral iliac crest. Additionally, clusters of 4 tracking markers were placed on the distal posterior thigh and the posterior lateral shank. A cluster of 3 individual rear-foot markers were placed directly over the calcaneus and projected through holes in the heel counters of the laboratory shoe.15 Marker placement and testing were completed by 2 trained laboratory researchers using a marker set that has been shown to be reliable within and between days.18 * Nike Inc, One Bowerman Dr, Beaverton, OR 97005. The gait analysis was then performed. After a standing calibration, the anatomical markers were removed, leaving the tracking markers for the walking trials. Each participant’s intentional walking speed was determined with photocells as the participant traversed a 25-m walkway. Intentional walking speed was defined as the speed that the participants would use to walk to and from a mailbox. Once determined, the speed was maintained within ⫾5% for all trials on the basis of feedback from the photocells. Data from a minimum of 5 usable trials were collected. A 6-camera motion analysis system† sampling at 120 Hz was used to capture the individual marker. Kinetic data were captured with a force platform‡ sampling at 1,080 Hz. The force platform was located at approximately the midpoint of the participant’s gait path during the trials. Kinematic data were filtered with a low-pass filter at 8 Hz and a fourth-order, zero-lag Butterworth filter. Kinetic data were filtered with a low-pass filter at 50 Hz and a fourth-order, zero-lag Butterworth filter. All inverse dynamic and joint kinematic calculations (Euler sequence X-Y-Z)19 were performed with Visual 3D software.§ Outcome Measures The kinematic variables of interest were the peak angle, angular excursion, and the peak moment in the frontal plane for the rear foot, knee, and hip. Peak angle was defined as the maximum value during the stance phase of gait. Angular excursion was defined as the peak angle during the stance phase subtracted from the initial angle at heel-strike. The kinetic variables of interest were the peak knee abduction moment, † Vicon-UK, 14 Minns Business Park, West Way, Oxford OX2 0JB, United Kingdom. ‡ Bertec Corp, 6171 Huntley Rd, Suite J, Columbus, OH 43229. § C-Motion Inc, 20030 Century Blvd, Suite 104A, Germantown, MD 20874. Volume 91 Number 8 Physical Therapy f 1237 Frontal-Plane Gait Mechanics in Knee Osteoarthritis Table 1. Descriptive Statistics for the Study Participants Variable Age, y, X (SD) 2 Body mass index, kg/m , X (SD) Medial Knee Osteoarthitis Group Control Group Lateral Knee Osteoarthritis Group 66.2 (7.8)a 56.3 (10.7)b 65.7 (6.4)a 32.2 (7.9) 27.8 (5.7) 30.4 (7.5) 1.4 (0.2) 1.5 (0.1) 1.4 (0.3) Walking speed, m/s, X (SD) Kellgren-Lawrence grade, n (%) a b 2 5 (33) Not applicable 3 (20) 3 4 (27) Not applicable 5 (33) 4 6 (40) Not applicable 7 (47) Value was significantly different from that for participants in the control group. Value was significantly different from that for participants with lateral knee osteoarthritis. the peak inversion moment, and the peak hip abduction moment. Moment data were expressed as internal moments and were normalized to body weight (in kilograms) and height (in meters). Data for the variables of interest were extracted from 5 individual trials and then averaged. Data Analysis A one-way ANOVA was used to analyze group differences for the vari- ables of interest. In the case of statistical significance, post hoc tests (Tukey honestly significant difference) were used to further analyze the data (SPSS version 14㛳). The ANOVAs were performed with and without age as a covariate. Because age was not a significant covariate, only the results of the ANOVA without age as a covariate are presented 㛳 SPSS Inc, 233 S Wacker Dr, Chicago, IL 60606. to improve clarity. Corrections for multiple tests were made by use of post hoc testing with standard Bonferroni corrections for multiple comparisons. Chi-square analysis was used to examine the equality of the distribution of K-L grades between the medial knee OA and lateral knee OA groups. Statistical significance was set at a P value of ⬍.02. To correlate our results with those of prior studies, we made an a priori plan to compare the peak hip abduction moment for participants who had medial knee OA and a K-L grade of greater than or equal to 3 with that for participants in the control group.14 Only statistical differences that were beyond the error of the measurement are reported in this article.18 Role of the Funding Source This work was made possible by grant number NIH-RR16548 (Thomas Buchanan, primary investigator) from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH). The sole role of the Table 2. Variables of Interest Control Groupa Lateral Knee Osteoarthritis Groupa ⫺0.062 (0.031) ⫺0.065 (0.032) Medial Knee Osteoarthritis Groupa Variable Pb Ankle Peak inversion moment (N䡠m/kg䡠m) ⫺0.050 (0.045) 6.2 (5.0)c Peak eversion (°) Eversion excursion (°) 10.6 (5.6) .38 3.5 (2.7) 1.8 (3.1) .01 10.2 (3.7) 10.0 (2.6) .96 ⫺0.326 (0.078) ⫺0.193 (0.111)d ⬍.01 ⬍.01 Knee Peak abduction moment (N䡠m/kg䡠m) Peak adduction (°) Adduction excursion (°) ⫺0.420 (0.083)c,d 5.6 (4.0) c,d 1.1 (5.1) ⫺5.2 (5.9)d 6.9 (2.3) c,d 5.6 (3.1) 3.8 (1.9) .01 Hip Peak abduction moment (N䡠m/kg䡠m) ⫺0.631 (0.132) ⫺0.631 (0.120) ⫺0.659 (0.107) .90 Peak adduction (°) 5.6 (2.5) 7.1 (3.3) 8.5 (3.4) .04 Adduction excursion (°) 7.4 (3.3) 7.8 (3.3) 7.0 (3.2) .11 a Reported as mean (standard deviation). b Reported for the one-way analysis of variance. c Value was significantly different from that for participants with lateral knee osteoarthritis. d Value was significantly different from that for participants in the control group. 1238 f Physical Therapy Volume 91 Number 8 August 2011 Frontal-Plane Gait Mechanics in Knee Osteoarthritis funding source was monetary support for the completion of the study. The funding source had no role in data analysis or dissemination of the results of the study. Results There was no difference in body mass index among the groups. However, participants in the control group were approximately 10 years younger than those in the 2 OA groups (Tab. 1). There was no difference in the proportion of disease severity between participants with medial knee OA and those with lateral knee OA (Tab. 1). The knee abduction moments for all groups demonstrated a bimodal shape with a larger peak during the first half of the stance phase than during the second half of the stance phase. The peak abduction moment was significantly lower in participants with lateral knee OA than in participants in the control group and significantly lower in participants in the control group than in participants with medial knee OA (Tab. 2, Fig. 1). Similar results were observed for the peak knee adduction angle. The peak knee adduction angle occurred at approximately 25% of the stance phase for all groups (Tab. 2, Fig. 1). Knee adduction excursion in participants with lateral knee OA was significantly lower than that in participants with medial knee OA but was not significantly different from that in participants in the control group (Tab. 2, Fig. 1). In general, there were greater differences in knee joint kinetics and kinematics between the lateral knee OA and control groups than between the medial knee OA and control groups. The hip kinematic patterns appeared to differ among the groups upon visual inspection (Fig. 2). Despite an offset between participants with medial knee OA and participants in the control group, their 2 patterns August 2011 Figure 1. Knee frontal-plane angle and moment during the stance phase in participants with medial and lateral knee osteoarthritis (OA) and participants in the control group. Means are plotted for all groups; ⫾1 standard error of the mean bars are plotted for the control group only. were quite similar; participants in the control group exhibited more hip adduction than participants with medial knee OA throughout the stance phase. However, participants with lateral knee OA demonstrated a more defined and larger peak value during the early stance phase (Tab. 2, Fig. 2). Compared with participants with lateral knee OA, participants with medial knee OA exhibited a reduction in peak hip adduction of 2.9 degrees, although this reduction was not statistically significant (Tab. 2, Fig. 2). No differ- ences were observed in hip kinetics. All groups exhibited similar bimodal curves with no differences in peak hip abduction moments. To make comparisons with previous work examining hip abduction moments in people with more severe knee OA (K-L grade of ⱖ3), we performed a subset analysis. Similar to the findings for the entire group, no differences in hip abduction moments were observed among the groups when participants with more severe knee OA solely were considered. Volume 91 Number 8 Physical Therapy f 1239 Frontal-Plane Gait Mechanics in Knee Osteoarthritis Discussion The purpose of the present study was to compare the gait mechanics of people who have medial knee OA and lateral knee OA with those of people in a control group (Fig. 4). The results suggest that people with medial knee OA exhibit gait mechanics at the knee, hip, and ankle that are different from those of people with lateral knee OA. The peak knee abduction moment, peak knee adduction, knee adduction excursion, and peak rear-foot eversion were all higher in participants with medial knee OA than in participants with lateral knee OA. Participants in the control group typically exhibited mechanics that fell between those of participants with lateral knee OA and those of participants with medial knee OA. Figure 2. Hip frontal-plane angle and moment during the stance phase in participants with medial and lateral knee osteoarthritis (OA) and participants in the control group. Means are plotted for all groups; ⫾1 standard error of the mean bars are plotted for the control group only. At the ankle, rear-foot eversion patterns were similar among the groups. However, there was an offset in the patterns for all groups. The joint excursions were similar; however, there were significant differences in peak eversion. Participants with lateral knee OA exhibited less peak eversion than those in the control group. Participants in the control group exhibited less peak eversion than those with medial knee OA (Tab. 2, Fig. 3). In terms of frontal1240 f Physical Therapy Volume 91 plane kinetics, participants with medial knee OA and participants in the control group exhibited similar patterns during the first 25% of the stance phase, whereas participants with lateral knee OA and those in the control group exhibited similar patterns during the final 75% of the stance phase. However, the peak rear-foot inversion moments during the first half of the stance phase were not statistically different among the groups (Tab. 2, Fig. 3). Number 8 The higher peak knee adduction exhibited by participants with medial knee OA than by participants with lateral knee OA was expected (Figs. 1 and 4). We believe that this result is related to the increased knee adduction associated with the genu varus alignment that is typical of medial knee OA. The difference in peak knee adduction between lateral knee OA and medial knee OA was observed previously.13 Weidow et al13 reported even larger differences (18°) in knee adduction between these groups than we reported in the present study (10.8°). However, these researchers presented the median value for each group, which may yield a larger difference than the mean value reported in the present study.13 The difference in knee adduction excursion between the groups was similar to the difference in peak knee adduction; participants with medial knee OA exhibited more excursion than participants with lateral knee OA. Our findings regarding the knee kinetics were consistent with those of others; the highest knee abducAugust 2011 Frontal-Plane Gait Mechanics in Knee Osteoarthritis tion moments were seen in participants with medial knee OA, and the lowest were seen in participants with lateral knee OA.13,14 Previous research suggested that the peak knee abduction moment is correlated with load in the medial compartment of the knee joint.20 Combined with our findings, this notion suggests that people with medial knee OA exhibit elevated loads in the medial compartment compared with people without the disease. In contrast, people with lateral knee OA likely exhibit reduced loads in the medial compartment; thus, more of the load may be distributed in the lateral compartment in these people. Differences in rear-foot mechanics between people with medial knee OA and people with lateral knee OA have yet to be reported in the literature. However, alterations in knee mechanics are likely to lead to changes at the foot (Fig. 3). Typically, genu valgus is associated with rear-foot eversion and genu varus is associated with rear-foot inversion.12 However, we found that participants with medial knee OA exhibited more peak eversion than those with lateral knee OA. Because the overall excursions were similar in these groups, the differences in peak values were attributed to differences at the time of heel-strike. These differences remained fairly constant throughout the stance phase. The values for participants in the control group fell between those for participants in the other 2 groups (Fig. 3). Although the findings were in contrast to our hypothesis, we believe that they indicate a compensatory mechanism of the foot to remain plantigrade. For example, because genu varus is typically associated with medial knee OA, the foot is likely positioned in increased inversion before heel-strike. Therefore, increased eversion is needed to obtain a plantigrade position. The August 2011 Figure 3. Rear-foot frontal-plane angle and moment during the stance phase in participants with medial and lateral knee osteoarthritis (OA) and participants in the control group. Means are plotted for all groups; ⫾1 standard error of the mean bars are plotted for the control group only. opposite is true for genu valgus, which is associated with lateral knee OA. This conceptual model recently was supported by researchers who observed increased rear-foot eversion in people with genu varum.21 It is interesting that the offsets seen in rear-foot kinematics were not mirrored in the kinetics (Fig. 3). For example, given the increased rearfoot eversion seen in people with medial knee OA, increased inversion moments would be expected. However, people with medial knee OA, on average, exhibited the lowest inversion moments throughout most of the stance phase. The results of the present study provide valuable information regarding conservative treatments for both medial knee OA and lateral knee OA. The differences in lower-extremity mechanics between people with Volume 91 Number 8 Physical Therapy f 1241 Frontal-Plane Gait Mechanics in Knee Osteoarthritis participants in either OA group by approximately 10 years. However, there is currently no evidence to suggest that this age difference would significantly influence our variables of interest. Additionally, our statistical analysis revealed that age was not a significant covariate in the present study. Two variables, body mass index and walking speed, which were controlled in our study, have been established as affecting gait mechanics.28,29 Both of these variables were similar in participants in the control group and those in the OA groups. Figure 4. Diagram of the posterior view of the left lower extremity in participants with lateral (left) and medial (right) knee osteoarthritis (OA). Increased rear-foot inversion is needed for the foot to be plantigrade in the participant with lateral knee osteoarthritis (left), and increased rear-foot eversion is needed in the participant with medial knee osteoarthritis (right). medial knee OA and those with lateral knee OA support current interventions for knee OA. Treatment of knee OA can be accomplished directly with knee braces or indirectly with wedged foot orthoses.22,23 Our findings for the rear foot suggest that caution is needed in the application of medial and lateral wedging. For example, a lateral wedge is used to indirectly reduce knee adduction associated with medial knee OA.15,24,25 This reduced knee adduction is accomplished by increasing eversion of the foot. Our results suggest that people with medial knee OA already exhibit increased foot eversion as a compensatory measure for knee varus. Further eversion induced by a lateral wedge may increase the risk of foot pathologies that are associated with this motion, such as plantar fasciitis or posterior tibialis tendinitis. People 1242 f Physical Therapy Volume 91 with these preexisting conditions or excessive rear-foot compensation might be better served by other approaches, such as gait retraining or hip strengthening, to address abnormal frontal-plane gait mechanics at the knee.26,27 The typical goal of these types of interventions is to provide a more proximal mechanism to alter loading at the knee. Such interventions would not so aggressively alter plantar loading and thus might be more successful in improving function in people with knee OA and a history of foot-related pathology. Regardless of the intervention, the results of the present study suggest that monitoring changes at the foot should be an important component of any intervention used to alter loading at the knee. We recognize that participants in the control group were younger than Number 8 The findings of the present study should dovetail into current knee OA research and practice in accounting for the entire kinetic chain of the lower extremity during evaluation or treatment of a patient with medial or lateral knee OA. Because of the nature of the study, extrapolation can be made only with respect to the frontal plane. Few studies have examined sagittal-plane changes, and fewer studies have assessed the transverse plane in patients with differential compartment involvement in knee OA.13 Thus, future studies examining changes in these planes and in different compartments involved in primary knee OA would be beneficial to the rehabilitation literature. Differences between compartments are typically not of concern for surgery, with the exceptions of extreme cases, because the hardware tends to correct malalignments. However, these differences are meaningful to health care providers who aim to improve function in patients with knee OA using a conservative approach. Initial research has suggested that patients with medial knee OA and those with lateral knee OA respond differently to similar interventions aimed at offloading the compartment in which the disease is progressing.15,24,25,30 The specificity of the response suggests that the development of cliniAugust 2011 Frontal-Plane Gait Mechanics in Knee Osteoarthritis cal prediction rules may help guide best practices in the conservative treatment of the disease. In summary, people with medial knee OA and those with lateral knee OA have significantly different frontal-plane gait mechanics at the knee, hip, and ankle. These differences should be taken into account in the development of interventions designed to treat degenerative joint diseases. As health care costs and knee injury rates continue to rise, the focus on conservative treatments for knee OA will continue to increase. We hope that the results of the present study will provide foundational evidence for effective interventions to mitigate the progression of knee OA and lead to healthier and more active lifestyles for patients with knee OA. All authors provided concept/idea/research design and project management. Dr Butler, Dr Barrios, and Dr Davis provided writing, data collection, and data analysis. Dr Royer and Dr Davis provided fund procurement. The authors thank Nike Inc for donating the footwear used for the laboratory experiment and New Balance Inc for donating the footwear used during the accommodation period of the study. The protocol for this study was reviewed and approved by the Institutional Review Board of the University of Delaware. A poster presentation of this work was given at the annual meeting of the American Society of Biomechanics; August 2004; Portland, Oregon. This work was made possible by grant number NIH-RR16548 (Thomas Buchanan, primary investigator) from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH). The contents of this article are solely the responsibility of the authors and do not necessarily represent the official views of the NCRR or the NIH. DOI: 10.2522/ptj.20100324 August 2011 References 1 Kauppila AM, Kyllonen E, Mikkonen P, et al. Disability in endstage knee osteoarthritis. Disabil Rehabil. 2009;31:370 –380. 2 Brandt KD. The pathogenesis of osteoarthritis. Rheumatol Rev. 1991;1:3–11. 3 Dillon CF, Rasch EK, Gu Q, Hirsch R. Prevalence of knee osteoarthritis in the United States: arthritis data from the Third National Health and Nutrition Examination Survey 1991–94. 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J Orthop Res. 2006;24:1890 –1899. 14 Mundermann A, Dyrby CO, Andriacchi TP. Secondary gait changes in patients with medial compartment knee osteoarthritis: increased load at the ankle, knee, and hip during walking. Arthritis Rheum. 2005; 52:2835–2844. 15 Butler RJ, Marchesi S, Royer T, Davis IS. The effect of a subject-specific amount of lateral wedge on knee mechanics in patients with medial knee osteoarthritis. J Orthop Res. 2007;25:1121–1127. 16 Cohen J. Statistical Power Analysis for the Behavioral Sciences. 2nd ed. Hillsdale, NJ: Lawrence Erlbaum Associates; 1988. 17 Kellgren JH, Lawrence JS. Radiological assessment of osteo-arthrosis. Ann Rheum Dis. 1957;16:494 –502. 18 Ferber R, McClay Davis I, Williams DS III, Laughton C. A comparison of within- and between-day reliability of discrete 3D lower extremity variables in runners. J Orthop Res. 2002;20:1139 –1145. 19 Grood ES, Suntay WJ. A joint coordinate system for the clinical description of threedimensional motions: application to the knee. J Biomech Eng. 1983;105:136 –144. 20 Andriacchi TP. Dynamics of knee malalignment. Orthop Clin North Am. 1994;25: 395– 403. 21 Barrios JA, Davis IS, Higginson JS, Royer TD. Lower extremity walking mechanics of young individuals with asymptomatic varus knee alignment. J Orthop Res. 2009; 27:1414 –1419. 22 Raja K, Dewan N. Efficacy of knee braces and foot orthoses in conservative management of knee osteoarthritis: a systematic review. Am J Phys Med Rehabil. 2011;90: 247–262. 23 Pollo FE, Otis JC, Backus SI, et al. Reduction of medial compartment loads with valgus bracing of the osteoarthritic knee. Am J Sports Med. 2002;30:414 – 421. 24 Kakihana W, Akai M, Yamasaki N, et al. Changes of joint moments in the gait of normal subjects wearing laterally wedged insoles. Am J Phys Med Rehabil. 2004;83: 273–278. 25 Hinman RS, Payne C, Metcalf BR, et al. Lateral wedges in knee osteoarthritis: what are their immediate clinical and biomechanical effects and can these predict a three-month clinical outcome? Arthritis Rheum. 2008;59:408 – 415. 26 Barrios JA, Crossley KM, Davis IS. Gait retraining to reduce the knee adduction moment through real-time visual feedback of dynamic knee alignment. J Biomech. 2010;43:2208 –2213. 27 Thorp LE, Wimmer MA, Foucher KC, et al. The biomechanical effects of focused muscle training on medial knee loads in OA of the knee: a pilot, proof of concept study. J Musculoskelet Neuronal Interact. 2010; 10:166 –173. 28 Lai P, Leung A, Li A, Zhang M. Threedimensional gait analysis of obese adults. Clin Biomech. 2008;23:S2–S6. 29 Landry SC, McKean KA, Hubley-Kozey CL, et al. Knee biomechanics of moderate OA patients measured during gait at a selfselected and fast walking speed. J Biomech. 2007;40:1754 –1761. 30 Rodrigues PT, Ferreira AF, Pereira RM, et al. Effectiveness of medial-wedge insole treatment for valgus knee osteoarthritis. Arthritis Rheum. 2008;59:603– 608. Volume 91 Number 8 Physical Therapy f 1243 Research Report Test-Retest Reliability and Minimal Detectable Change Scores for Sit-toStand-to-Sit Tests, the Six-Minute Walk Test, the One-Leg Heel-Rise Test, and Handgrip Strength in People Undergoing Hemodialysis Eva Segura-Ortı́, Francisco José Martı́nez-Olmos E. Segura-Ortı́, PT, MSc, PhD, Department of Physiotherapy, Universidad CEU Cardenal Herrera, Avda Seminario s/n, 46113 Moncada (Valencia), Spain. Address all correspondence to Ms SeguraOrtı́ at: [email protected]. F.J. Martı́nez-Olmos, PT, MSc, Department of Physiotherapy, Universidad CEU Cardenal Herrera. [Segura-Ortı́ E, Martı́nez-Olmos FJ. Test-retest reliability and minimal detectable change scores for sit-to-stand-to-sit tests, the SixMinute Walk Test, the one-leg heel-rise test, and handgrip strength in people undergoing hemodialysis. Phys Ther. 2011;91: 1244 –1252.] © 2011 American Physical Therapy Association Published Ahead of Print: June 30, 2011 Accepted: April 8, 2011 Submitted: April 21, 2010 Background. Determining the relative and absolute reliability of outcomes of physical performance tests for people undergoing hemodialysis is necessary to discriminate between the true effects of exercise interventions and the inherent variability of this cohort. Objective. The aims of this study were to assess the relative reliability of sit-tostand-to-sit tests (the STS-10, which measures the time [in seconds] required to complete 10 full stands from a sitting position, and the STS-60, which measures the number of repetitions achieved in 60 seconds), the Six-Minute Walk Test (6MWT), the one-leg heel-rise test, and the handgrip strength test and to calculate minimal detectable change (MDC) scores in people undergoing hemodialysis. Design. This study was a prospective, nonexperimental investigation. Methods. Thirty-nine people undergoing hemodialysis at 2 clinics in Spain were contacted. Study participants performed the STS-10 (n⫽37), the STS-60 (n⫽37), and the 6MWT (n⫽36). At one of the settings, the participants also performed the one-leg heel-rise test (n⫽21) and the handgrip strength test (n⫽12) on both the right and the left sides. Participants attended 2 testing sessions 1 to 2 weeks apart. Results. High intraclass correlation coefficients (ⱖ.88) were found for all tests, suggesting good relative reliability. The MDC scores at 90% confidence intervals were as follows: 8.4 seconds for the STS-10, 4 repetitions for the STS-60, 66.3 m for the 6MWT, 3.4 kg for handgrip strength (force-generating capacity), 3.7 repetitions for the one-leg heel-rise test with the right leg, and 5.2 repetitions for the one-leg heel-rise test with the left leg. Limitations. A limited sample of patients was used in this study. Conclusions. The STS-16, STS-60, 6MWT, one-leg heel rise test, and handgrip strength test are reliable outcome measures. The MDC scores at 90% confidence intervals for these tests will help to determine whether a change is due to error or to an intervention. Post a Rapid Response to this article at: ptjournal.apta.org 1244 f Physical Therapy Volume 91 Number 8 August 2011 Physical Performance Tests and Hemodialysis E nd-stage renal disease was first considered a rare disease, but the yearly increase in prevalence in the United States outdated this definition 20 years ago.1 This increase in end-stage renal disease also has been found in Europe,2,3 where the prevalence per million people was 779 by December 2006 and increased to 881 by December 2008. During this period of time, the prevalence in Spain2,3 increased from 983 to 994. The most common renal replacement therapy is hemodialysis; less common treatments are renal transplantation and peritoneal dialysis. Old age and cardiovascular comorbidities are commonly found in patients with end-stage renal disease.1,2 Physical therapists are among the health care providers who supervise exercise interventions for patients receiving hemodialysis. Given the need to measure outcomes to assess changes in physical function, specific clinical tools for assessing treatment effects should be tested for reliability with patients receiving hemodialysis. Exercise interventions have been implemented in patients undergoing hemodialysis for almost 30 years. Outcome measures in most published studies include laboratory measures, such as the peak oxygen consumption in a graded exercise test.4 –7 This test may be difficult for older patients and patients with low levels of function to perform. In addition, despite research applicability, this test is not easy to perform in clinical settings. The identification of reliable physical performance tests for patients undergoing hemodialysis would enhance the ability to assess physical function levels and the effectiveness of interventions for both clinical and research purposes. A recent meta-analysis of exercise in patients undergoing hemodialysis8 concluded that aerobic, resistance, August 2011 or combined exercise programs resulted in an increase in peak oxygen consumption4 –7,9 –11 and in physical function measured with the Medical Outcomes Study 36-Item Short-Form Health Survey questionnaire.12,13 However, the effects of exercise on physical performance tests could not be reported because of the lack of uniformity of the tests used in published studies.8,14 Several physical performance tests were analyzed in the present study. The Six-Minute Walk Test (6MWT) is a physical function test that is frequently used to assess the impact of renal rehabilitation.12,15–22 The STS-10 (a sit-to-stand-to-sit [STS] test that measures the time [in seconds] required to complete 10 full stands from a sitting position) has been recommended to quantify lower-extremity muscle strength (force-generating capacity) in patients with lower-extremity weakness.23 The STS-60 (an STS test that measures the number of repetitions achieved in 60 seconds) has been used as a surrogate index of muscle endurance.20,24 The one-leg heel-rise test consists of repeated eccentric and concentric muscle actions and reflects endurance rather than strength in the plantar-flexor muscles.25 This test has shown that calf muscles are weak as early as the predialysis stage23; this weakness could contribute to an altered gait pattern.26 The maximal voluntary handgrip strength test is a quantitative and easily performed test that allow comparisons of people who are healthy and various clinical groups.27,28 Handgrip strength is necessary for optimal performance of activities of daily living, such as getting dressed and handling pans.29 Greater handgrip strength increases the probability of survival of patients undergoing dialysis.30 Studies assessing the reliability of these tests for people undergoing hemodialysis are uncommon.24,31 The reliability of a test should be expressed as both relative reliability and absolute reliability.32 Relative reliability may be measured with the intraclass correlation coefficient (ICC), which is used for test-retest reliability. Individual performance and measurement error are measured with absolute reliability, which provides information for differentiating a true change in performance from a change due to individual variation and measurement error. The aims of this study were to calculate the test-retest reliability of commonly used physical performance tests in people undergoing hemodialysis (6MWT, STS-10, STS-60, oneleg heel-rise test, and handgrip strength test) and to calculate absolute reliability with the standard error of measurement (SEM) and minimal detectable change (MDC) scores at 90% confidence intervals (MDC90). Method Design This study was a prospective, nonexperimental, descriptive methodological investigation. Setting and Participants Study participants were recruited from 2 hemodialysis clinics in Valencia, Spain, from 2006 to 2008. Inclusion criteria were evaluated by the participant’s nephrologist, who gave authorization before solicitation of interest. The inclusion criteria were receipt of recurring hemodialysis for 3 months or more with adequate dialysis delivery (Kt/Vⱖ1.2)* and the absence of acute or chronic medical conditions that would preclude the collection of outcome measure data. * The most common method to calculate the amount of hemodialysis per patient is by the calculation of Kt/V around 1.2, where K is urea clearance, t is the length of the hemodialysis session, and V is the patient’s water volume.33 Volume 91 Number 8 Physical Therapy f 1245 Physical Performance Tests and Hemodialysis Exclusion criteria were recent myocardial infarction (within 6 weeks), malignant arrhythmias, unstable angina, and any disorder that was exacerbated by activity. Demographic and clinical data were collected from the medical history and included age, sex, body mass index, time on hemodialysis, hemoglobin level, cause of kidney disease, and comorbidities. All participants provided written informed consent. Procedure Participants performed each of the tests twice, with a 1- to 2-week interval between the testing sessions, always on a dialysis day, and immediately before the second or third hemodialysis session of the week. Every effort was made to keep all factors associated with the testing sessions consistent: day of the week, time of day, staff member administering the test, and area in which the test was performed. Participants performed the STS tests, the 6MWT, the one-leg heel-rise test, and the handgrip strength test. STS-10 and STS-60. Both STS tests were performed immediately before the second hemodialysis session of the week. The STS-10 was performed first, and the STS-60 was performed 10 minutes later, when the heart rate and blood pressure had decreased to baseline levels. The STS-10 measured the time (in seconds) required to perform 10 consecutive repetitions of sitting down on and getting up from a chair. Participants were instructed to perform the task “as fast as possible,” starting and finishing at the sitting position. Participants were allowed a practice trial before the beginning of the test. They began the test by crossing their arms on their chest and sitting with their back against the chair.34 For the STS tests and for the 6MWT, heart rate (Polar S610i†) and blood pressure (Omron HEM-711AC‡) were measured immediately before and after the tests to monitor the physiological and clinical status of the participants during the tests and to obtain additional information about the repeat assessment conditions. The time taken to perform the STS-10 and the degree of difficulty, determined as the rate of perceived exertion (RPE, measured with a Borg scale from 6 to 20), were recorded at the end of the test. Csuka and McCarty35 first described the use of the STS test as a measure of lower-extremity strength (forcegenerating capacity of muscle). The test was performed with a chair that had no armrests, measured about 44.5 cm high and 38 cm deep, and was backed up against a wall to minimize the risk of falling.36 Although this test is nonspecific, it is simple, inexpensive, rapid, and reproducible35 and is included in the battery of tests used for people with renal disease.17,18,20,37 The STS-60 measured the number of repetitions of sitting down on and getting up from a chair achieved in 60 seconds. Heart rate and blood pressure were measured immediately before and after the test. The number of repetitions achieved and the degree of difficulty (measured as RPE⫽6 –20) were recorded at the end of the test. Each repetition started and finished at the sitting position, and if a participant was standing when the time was over, it was considered half a repetition. Participants were allowed to stop if rest was needed and to continue performing the task until the 60 seconds † Polar Electro Oy, HQ Professorintie 5, FIN90440 Kempele, Finland. ‡ Omron Europe BV, Wegalaan 67-69, 2132 JD Hoofddorp, the Netherlands. 1246 f Physical Therapy Volume 91 Number 8 were over. The STS-60 has been found to be a valid measure of lowerbody strength.38 6MWT. The 6MWT was undertaken immediately before the third hemodialysis session of the week because by the end of the week, the extra fluid retained by the participants was at its lowest level, minimizing its influence on the test results. The 6MWT was performed in a 20-m corridor located in the hemodialysis unit; tape was placed every 2 m. Participants were asked to walk the longest distance possible in 6 minutes by walking continuously the 20 m indicated on the floor, turning around at the final mark without stopping, and covering as much ground as possible.39 The standardized order given to the participants was, “Walk as far as possible for 6 minutes, but don’t run or jog.”40 Participants were allowed to use any ambulation aid that they used normally in daily life. They could stop if needed and restart later. Heart rate and blood pressure were measured immediately before and after the test. The distance covered (in meters) and the degree of difficulty (determined as the RPE) were recorded at the end of the test. The 6MWT is considered to be a better indicator of the ability to perform activities that resemble those of daily living, such as walking, than physiological exercise capacity testing.16 The latter usually requires people to perform at maximal or nearly maximal levels and in laboratory-based environments and involves techniques and tasks with which people are not always familiar. One-leg heel-rise test. The oneleg heel-rise test was undertaken immediately before the second hemodialysis session of the week. This test was used to measure the functional strength of the triceps surae muscle in each leg and was August 2011 Physical Performance Tests and Hemodialysis performed only with socks (no footwear). The rhythm, one lift every other second, was paced with a metronome. Before the test, participants were asked to maintain balance while standing on one leg41 by touching the wall with the fingertips, arms away from the body, and to avoid pushing their arms against the wall and thereby shifting their weight. The contralateral foot was held just above the floor. After one trial with the left foot to allow the participants to become familiar with the testing procedure, the test was performed with the right foot. Participants were instructed to lift the heel as high as possible at the metronome frequency until no further heel rises could be performed due to exhaustion. The test was terminated if a participant’s knee flexed or if a participant leaned or pushed against the wall, according to the examiner’s observation. The test was performed to a maximum of 25 repetitions because this is the average number of repetitions performed by people who are healthy.25,42 After the test, the number of repetitions per leg and the degree of difficulty (determined as the RPE) were recorded. Handgrip strength dynamometry. The handgrip strength test was performed immediately before the third hemodialysis session of the week. A handgrip dynamometer (Takei Physical Fitness Test TKK 5401 Grip Dynamometer§) was used to measure the amount of strength developed by each hand in this functional task. Participants were positioned standing with the elbow extended at the moment of the test, according to the manufacturer’s instructions. Three consecutive repetitions of 3 seconds, with 15 seconds of rest between the repetitions, were performed with both arms, starting with the dominant arm. Verbal encouragement was given during the task. The highest peak force per arm was recorded. Data Analysis The SPSS package version 15.0 for Windows㛳 was used for data management and analysis. The level of significance was predetermined to be Pⱕ.05 for all statistical analyses. Data are reported as mean (standard deviation), if normally distributed, or as median (range). The KolmogorovSmirnov test, skewness, and kurtosis were used to assess whether the data were normally distributed. Paired comparisons to assess for systematic bias between trial weeks were performed with the paired t test or the Wilcoxon signed rank test. The testretest reliability of data for all repeated tests was assessed with the ICC (model alpha), 2-way randomeffects model, which is appropriate for the present study design. The test-retest reliability of data for the physical performance tests (6MWT, STS-10, STS-60, one-leg heel-rise test, and handgrip strength test) was assessed with the ICC (2,1) because there was only one test score from each session. The results for intraobserver reliability are presented because the same physical therapist administered all of the tests. An ICC above .75 was considered to demonstrate good reliability, although for clinical measures it has been suggested that the ICC should exceed .90.43 The ICC indicates similar patterns of scores in several sets of data; thus, it checks for consistency rather than absolute agreement in measurements. Thus, if relative reliability is high, regardless of whether the precise scores given by 2 evaluators differ, then in both cases good performance receives higher scores than average performance and average August 2011 The SEM and the MDC90 were calculated with the following formulas44: SEM ⫽ SD ⫻ 冑共1 ⫺ r), where r⫽ICC for the participant group, and MDC 90 ⫽ SEM ⫻ 1.65 ⫻ 冑2. The SEM measures absolute reliability and represents the extent to which a variable can vary in the measurement process.45 Because some error may be present in a measurement, a range of values is often reported. A measurement of ⫾1 SEM represents a 68% confidence interval. Both 90% and 95% confidence intervals have been used to describe the MDC.32,46,47 To be 90% confident about the range for a measurement, the calculation 1.68 ⫻ SEM should be used. Minimal detectable change is defined as the amount of change in a measurement necessary to conclude that the difference is not attributable to error; it is the smallest change that falls outside the expected range of error.45,46 Any change exceeding the MDC90 is considered true change. The delta (change) scores within each trial (scores after the test minus scores before the test) for heart rate and blood pressure in the STS tests and the 6MWT and data on the RPE were reported, and pairwise comparisons between trials were done with the paired t test or the Wilcoxon signed rank test. Role of the Funding Source This study was supported by a grant from Universidad CEU Cardenal Herrera (PRUCH 06/08). Results § Takei Scientific Instruments Co Ltd, No. 619, Yashiroda, Akiha-Ku, Niigata City, Niigata Prefecture, 956-0113 Japan. performance receives higher scores than poor performance. 㛳 SPSS Inc, 233 S Wacker Dr, Chicago, IL 60606. Data were collected from 39 participants (7 women and 32 men). Some Volume 91 Number 8 Physical Therapy f 1247 Physical Performance Tests and Hemodialysis Participants undergoing hemodialysis in 2 settings (N=39) 1 participant could not perform the second test due to worsened health; 1 participant was unwilling to attend the second test 1 participant could not perform the second test due to worsened health; 1 participant was unwilling to attend the second test 1 participant could not perform the second test due to a complicated ulcer on the foot; 2 participants were unwilling to attend the second test One setting was not conducive to the 1leg heel-rise test (12 participants did not perform the test at that setting), and 6 participants from the other setting were unwilling to attend the test One setting was not conducive to the handgrip test (12 participants did not perform the test at that setting), and 15 participants from the other setting were unwilling to attend the test STS-10 data from 37 participants STS-60 data from 37 participants 6MWT data from 36 participants One-leg heel-rise test data from 21 participants Handgrip strength test data from 12 participants Figure. Flow chart for study participants. STS-10⫽a sit-to-stand-to-sit (STS) test that measures the time (in seconds) required to complete 10 full stands from a sitting position, STS-60⫽an STS test that measures the number of repetitions achieved in 60 seconds, 6MWT⫽Six-Minute Walk Test. demographic data were not available (eg, no height for one participant). One setting was not conducive to the performance of the handgrip and one-leg heel-rise tests, so these tests were not performed with participants in that setting. The flow chart (Figure) shows the number of participants who performed each test. No adverse events occurred during testing. Descriptive statistics for the 39 participants are shown in Table 1. In 3 participants, the fistula was located in the dominant arm. The results of repeated tests are shown in Table 2. The distance walked during the 6MWT was significantly greater in trial 2. The ICCs for test-retest reli1248 f Physical Therapy Volume 91 ability were high for all of the outcome measures (STS-10, STS-60, 6MWT, and one-leg heel-rise test on the right and left sides). Data for the handgrip test with the dominant and nondominant arms were calculated for 12 participants. There were no significant differences between trial 1 and trial 2. For the dominant arm, the means (standard deviations) in trial 1 and trial 2 were 26.9 (7.3) kg and 25.9 (7.1) kg, respectively (P⫽.083); for the nondominant arm, the means (standard deviations) in trial 1 and trial 2 were 23.8 (6.6) kg and 23.4 (7.1) kg, respectively (P⫽.594). The ICCs for the dominant and nondominant arms were .96 (95% confidence interval⫽.88 – .99) and .95 (95% confidence inter- Number 8 val⫽.83–.98), respectively. The repeated-measures SEM and MDC90 are shown in Table 3. Delta scores within trial 1 and trial 2 for heart rate and blood pressure in the STS tests and the 6MWT are shown in Table 4. For the 3 physical function tests, the delta score for heart rate was significantly higher in trial 1. There were no differences between trials in the delta score for blood pressure or the RPE. Discussion Our findings demonstrated that the test-retest reliability (relative reliability) of the clinical tests was excellent. All measures were found to have high test-retest reliability, with August 2011 Physical Performance Tests and Hemodialysis Table 1. been reported. The high test-retest reliability found for the one-leg heelrise test in the present study is similar to values found in patients with chronic heart failure (ICC⫽.94).51 The ICC of the handgrip strength test was high, despite the small sample, in agreement with data from patients with cervical radiculopathy (ICC⫽.85–.98).52 Our findings consistently showed high test-retest reliability in all of the physical performance tests. Factors that may explain the high ICCs in all of the physical performance tests are consistent timing of the tests (same day of the week, before the hemodialysis session) and standardization of the evaluator’s instructions. Demographic and Clinical Data for Study Participants (N⫽39) Characteristic Value Age, y, X (SD) 60.3 (15.8) Sex, no. of women:men 7:32 Handedness, no. who were right handed:left handed a 10:2 Body mass index, kg/m2, X (SD)b 22.0 (3.3) Time on hemodialysis, mo, median (range) 25 (6–152) Hemoglobin level, X (SD) 11.3 (1.4) Cause of kidney disease (no. of participants) Diabetes mellitus 8 Glomerulonephritis 9 Nephroangiosclerosis 8 Lupus 1 Interstitial nephropathy 1 Other 12 No. of comorbidities, median (range) a b 3 (1–5) n⫽12. n⫽38. only the STS-10 having values slightly below the threshold of .90 for minimal acceptable reliability for a clinical test.43 In the present study, we calculated an ICC of .94 for the test-retest reliability of the 6MWT. No previous determinations of the ICC of this test in people undergoing hemodialysis exist, although reported values in other populations32,46,48,49 are consistent (ICC⫽.94 –.98) with our results. The STS tests have not been widely used in people undergoing hemodialysis; however, the ICCs of these tests in people who are candidates for a renal transplant (.84),31 adult populations (.80),38 and people with chronic low back pain (.91)50 have The results of the present study demonstrated that although the testretest reliability was excellent, there was still a substantial degree of variability in performance for individual participants from 1 test session to the next, as shown by the SEM and MDC90 values (Tab. 3). Because the SEM is based on the assumption of a normal distribution, the probabilities of a normal curve can be applied, and the values from Table 3 can be translated to clinical practice use. Thus, there is a 68% probability that Table 2. Reliability Results for Physical Performance Tests in People Undergoing Hemodialysisa X (SD) Median (Range) ICC for Trial 1 vs Trial 2 95% CI for ICC P for Significance of Difference Between Trial 1 and Trial 2 24.0 (10.9) 21.6 (9.5–54.1) .88 .78–.94 .059b 25.5 (9.4) 24 (11–39) .97 .94–.98 .966b .94 .89–.97 .002c Trial 1 No. of Participants X (SD) STS-10 (s) 37 25.1 (10.4) STS-60 (repetitions) 37 25.6 (9.8) 6MWT (m) 36 425.2 (116.0) One-leg heel-rise, right (repetitions) 21 10.8 (9.2) 7 (0–25) 11.6 (9.2) 9 (0–25) .97 .92–.99 .138b One-leg heel-rise, left (repetitions) 21 10.6 (9.1) 8 (0–25) 10.7 (9.0) 7 (0–25) .94 .85–.97 .505b Test Median (Range) Trial 2 22 (10.6–53.9) 24.5 (10–56) 445.9 (106.3) a ICC⫽intraclass correlation coefficient, CI⫽confidence interval, STS-10⫽a sit-to-stand-to-sit (STS) test that measures the time (in seconds) required to complete 10 full stands from a sitting position, STS-60⫽an STS test that measures the number of repetitions achieved in 60 seconds, 6MWT⫽Six-Minute Walk Test. b As determined with the Wilcoxon signed rank test of paired samples. c As determined with the paired-samples t test (t⫽⫺3.323). August 2011 Volume 91 Number 8 Physical Therapy f 1249 Physical Performance Tests and Hemodialysis Table 3. Standard Error of Measurement (SEM) for Repeated Measures and Minimal Detectable Change Scores at 90% Confidence Intervals (MDC90) for Various Testsa Test SEM MDC90 3.6 8.4 STS-10 (s) STS-60 (repetitions) 1.7 4.0 28.4 66.3 Handgrip strength, dominant arm (kg) 1.5 3.4 Handgrip strength, nondominant arm (kg) 1.5 3.4 One-leg heel-rise, right (repetitions) 1.6 3.7 One-leg heel-rise, left (repetitions) 2.2 5.2 6MWT (m) a STS-10⫽a sit-to-stand-to-sit (STS) test that measures the time (in seconds) required to complete 10 full stands from a sitting position), STS-60⫽an STS test that measures the number of repetitions achieved in 60 seconds, 6MWT⫽6-minute walk test. a repeated measure of a test will be within 1 SEM of the original score, and there is a 96% probability that a repeated measure will be within 2 SEMs. This information could be useful for discriminating between true change and variability of performance, according to the SEM, in an examination of the repeat performance of people undergoing hemodialysis. The 6MWT was the only outcome measure that was previously assessed for absolute reliability, in Alzheimer disease32 and Parkinson disease46; high individual variability was reported in both studies. Ries et al32 reported an ICC of .98, a SEM of 20 m, and an MDC90 of 37 m, and Steffen and Seney46 reported an ICC of .96 and an MDC95 of 82 m. Our results also revealed high variability, with an MDC90 of 66 m. Even though measurement conditions were strictly replicated, variations in the physiological and clinical status of the participants undergoing hemodialysis could have accounted for some of the heterogeneity in the results. The delta scores for the heart rate in the 6MWT, STS-10, and STS-60 were significantly higher in the first trial than in the second trial (Tab. 4), although medications were kept constant and the perceived exertion did not change. This lack of homogeneity also was found in the results reported for the 6MWT in the literature; for example, distances of 347 to 522 m were found.15,17,18,21,53 Age was not found to affect the high variability observed in the present study (results not shown). The significant difference in meters walked between trial 1 and trial 2 can be explained by the practice effect of the test,16 which could be prevented by adding a practice trial. The results reported in the literature for the STS Table 4. Heart Rate (HR), Systolic Blood Pressure (SBP), Diastolic Blood Pressure (DBP), and Rate of Perceived Exertion (RPE) in Response to Various Testsa Trial 1 Test 6MWT STS-10 Parameter Delta score for HR (bpm) 19.5 (⫺2 to 66) No. of Participants Median (Range) in Trial 2 No. of Participants 38 16 (2 to 63) 36 .038 Delta score for SPB (mm Hg) 15 (⫺37 to 55) 31 11.5 (⫺18 to 65) 30 .829 Delta score for DBP (mm Hg) 3 (⫺24 to 27) 31 1 (⫺17 to 35) 30 .636 36 .369 37 .001 RPE 11 (7 to 16) 38 Delta score for HR (bpm) 11 (0 to 49) 38 Delta score for SPB (mm Hg) Delta score for DBP (mm Hg) STS-60 Median (Range) in Trial 1 P for Significance of Difference Between Trial 1 and Trial 2 Trial 2 2 (⫺23 to 31) ⫺2 (⫺18 to 9) 11 (7 to 17) 6 (⫺6 to 27) 31 2 (⫺36 to 40) 29 .682 31 0 (⫺19 to 13) 29 .194 RPE 11 (7 to 13) 38 11 (7 to 17) 37 .850 Delta score for HR (bpm) 18 (0 to 58) 37 14 (⫺18 to 62) 37 .018 Delta score for SPB (mm Hg) 8 (⫺34 to 62) 31 8 (⫺52 to 39) 33 .381 Delta score for DBP (mm Hg) 0 (⫺26 to 25) 31 ⫺1 (⫺24 to 62) 33 .751 38 13 (11 to 17) 37 .673 RPE 13 (11 to 17) a 6MWT⫽Six-Minute Walk Test, delta score⫽score after the test minus score before the test within the trial, bpm⫽beats per minute, STS-10⫽a sit-to-standto-sit (STS) test that measures the time (in seconds) required to complete 10 full stands from a sitting position, STS-60⫽an STS test that measures the number of repetitions achieved in 60 seconds. 1250 f Physical Therapy Volume 91 Number 8 August 2011 Physical Performance Tests and Hemodialysis tests in patients undergoing hemodialysis also showed some heterogeneity, with results ranging from 21 to 29 seconds on the STS-1011,17,18,21 and 22 repetitions on the STS-60.24 The RPEs for the 6MWT and the STS tests were lower than expected, although they were in agreement with the results of previous research.54 An underestimation of RPEs has been observed clinically and practically.16,55 Handgrip strength for the right arm and the left arm in the present study were 26.9 and 23.8 kg, respectively; these values were lower than those reported in a previous study (41.6 kg for the right arm and 39.9 kg for the left arm).18 We found that fistula location had no effect on handgrip strength (results not shown). Future studies with a larger number of participants should include results related to sex and age.56 One-leg heel-rise repetitions in the present study were below 25, the value established as normal in 2 studies.25,42 Jan et al57 showed that the ability to repeat heel rises was closely related to age and sex in a study in which adults who were healthy and older than 60 years of age achieved only 20 or fewer repetitions. Because people in poor physical condition are not able to perform a single repetition, future studies are needed to clarify whether the floor effect of this test allows discrimination among people with different physical conditions. Additionally, this test is difficult for only one observer to control because control of both flexion of the knee and leaning or pushing against the wall is required. The present study indicated that the 6MWT, STS-10, STS-60, one-leg heelrise test, and handgrip strength test are reliable measures. Clinicians are encouraged to understand how changes in scores translate to clinical practice. On the basis of our results, if a change exceeding ⫾66 m (MDC90) August 2011 occurs in the 6MWT, clinicians can be 90% confident that the difference is not due to measurement error or variability among participants. Clinicians could arrive at similar conclusions for all tests being evaluated. In conclusion, the results of the present study demonstrated excellent test-retest reliability for the 6MWT, STS-10, STS-60, one-leg heel-rise test, and handgrip strength test in people undergoing hemodialysis. Despite high ICCs for absolute reliability, there was important individual variability in the performance of these measures. The SEM and MDC90 values for each of the tests provide clinicians with thresholds for identifying changes beyond those expected from measurement error and individual variability. This information will help in monitoring performance changes over time and assessing the effectiveness of exercise interventions in people undergoing hemodialysis. Both authors provided concept/idea/research design, data collection and analysis, participants, facilities/equipment, and consultation (including review of manuscript before submission). Ms Segura-Ortı́ provided writing and project management. The study was approved by the ethical review boards of the Universidad CEU Cardenal Herrera and the Fundación Hospital General Universitario de Valencia, Valencia, Spain. This study was supported by a grant from Universidad CEU Cardenal Herrera (PRUCH 06/08). DOI: 10.2522/ptj.20100141 References 1 US Renal Data System, ed. USRDS 2009 Annual Data Report: Atlas of Chronic Kidney Disease and End-Stage Renal Disease in the United States. Bethesda, MD: National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health; 2009. 2 ERA-EDTA Registry. ERA-EDTA Registry Annual Report 2008. Amsterdam, the Netherlands: Department of Medical Informatics; 2010. 3 ERA-EDTA Registry. ERA-EDTA Registry Annual Report 2006. Amsterdam, the Netherlands: Department of Medical Informatics; 2008. 4 Painter P, Moore G, Carlson L, et al. Effects of exercise training plus normalization of hematocrit on exercise capacity and health-related quality of life. Am J Kidney Dis. 2002;39:257–265. 5 Goldberg AP, Geltman EM, Hagberg JM, et al. Therapeutic benefits of exercise training for hemodialysis patients. Kidney Int Suppl. 1983;16:S303–S309. 6 Konstantinidou E, Koukouvou G, Kouidi E, et al. Exercise training in patients with end-stage renal disease on hemodialysis: comparison of three rehabilitation programs. J Rehabil Med. 2002;34:40 – 45. 7 Kouidi E, Iacovides A, Iordanidis P, et al. Exercise renal rehabilitation program: psychosocial effects. Nephron. 1997;77:152– 158. 8 Segura-Ortı́ E. Exercise in haemodyalisis [sic] patients: a literature systematic review [in Spanish]. Nefrologia. 2010;30: 236 –246. 9 Deligiannis A, Kouidi E, Tassoulas E, et al. Cardiac effects of exercise rehabilitation in hemodialysis patients. Int J Cardiol. 1999;70:253–266. 10 Deligiannis A, Kouidi E, Tourkantonis A. Effects of physical training on heart rate variability in patients on hemodialysis. Am J Cardiol. 1999;84:197–202. 11 van Vilsteren MC, de Greef MH, Huisman RM. The effects of a low-to-moderate intensity pre-conditioning exercise programme linked with exercise counselling for sedentary haemodialysis patients in the Netherlands: results of a randomized clinical trial. Nephrol Dial Transplant. 2005; 20:141–146. 12 Cheema B, Abas H, Smith B, et al. Progressive exercise for anabolism in kidney disease (PEAK): a randomized, controlled trial of resistance training during hemodialysis. J Am Soc Nephrol. 2007;18:1594 – 1601. 13 Johansen KL, Painter PL, Sakkas GK, et al. Effects of resistance exercise training and nandrolone decanoate on body composition and muscle function among patients who receive hemodialysis: a randomized, controlled trial. J Am Soc Nephrol. 2006; 17:2307–2314. 14 Segura-Ortı́ E, Johansen KL. Exercise in end-stage renal disease. Semin Dial. 2010; 23:422– 430. 15 Fitts SS, Guthrie MR, Blagg CR. Exercise coaching and rehabilitation counseling improve quality of life for predialysis and dialysis patients. Nephron. 1999;82:115– 121. 16 Fitts SS, Guthrie MR. Six-minute walk by people with chronic renal failure: assessment of effort by perceived exertion. Am J Phys Med Rehabil. 1995;74:54 –58. 17 Levendoglu F, Altintepe L, Okudan N, et al. A twelve week exercise program improves the psychological status, quality of life and work capacity in hemodialysis patients. J Nephrol. 2004;17:826 – 832. Volume 91 Number 8 Physical Therapy f 1251 Physical Performance Tests and Hemodialysis 18 Headley S, Germain M, Mailloux P, et al. Resistance training improves strength and functional measures in patients with endstage renal disease. Am J Kidney Dis. 2002;40:355–364. 19 Heiwe S, Clyne N, Tollback A, Borg K. Effects of regular resistance training on muscle histopathology and morphometry in elderly patients with chronic kidney disease. Am J Phys Med Rehabil. 2005;84: 865– 874. 20 Segura-Ortı́ E, Rodilla-Alama V, Lisón JF. Physiotherapy during hemodialysis: results of a progressive resistance-training programme [in Spanish]. Nefrologia. 2008;28:67–72. 21 Painter P, Carlson L, Carey S, et al. Physical functioning and health-related quality-oflife changes with exercise training in hemodialysis patients. Am J Kidney Dis. 2000;35:482– 492. 22 DePaul V, Moreland J, Eager T, Clase CM. The effectiveness of aerobic and muscle strength training in patients receiving hemodialysis and EPO: a randomized controlled trial. Am J Kidney Dis. 2002;40: 1219 –1229. 23 Brodin E, Ljungman S, Sunnerhagen KS. Rising from a chair: a simple screening test for physical function in predialysis patients. Scand J Urol Nephrol. 2008;42: 293–300. 24 Koufaki P, Mercer TH, Naish PF. Effects of exercise training on aerobic and functional capacity of end-stage renal disease patients. Clin Physiol Funct Imaging. 2002;22:115–124. 25 Svantesson U, Osterberg U, Thomee R, Grimby G. Muscle fatigue in a standing heel-rise test. Scand J Rehabil Med. 1998; 30:67–72. 26 Meinders M, Gitter A, Czerniecki JM. The role of ankle plantar flexor muscle work during walking. Scand J Rehabil Med. 1998;30:39 – 46. 27 van Wetering CR, van Nooten FE, Mol SJ, et al. Systemic impairment in relation to disease burden in patients with moderate COPD eligible for a lifestyle program: findings from the INTERCOM trial. Int J Chron Obstruct Pulmon Dis. 2008;3:443– 451. 28 Schlussel MM, dos Anjos LA, de Vasconcellos MT, Kac G. Reference values of handgrip dynamometry of healthy adults: a population-based study. Clin Nutr. 2008; 27:601– 607. 29 Desrosiers J, Bravo G, Hebert R, Dutil E. Normative data for grip strength of elderly men and women. Am J Occup Ther. 1995; 49:637– 644. 30 Wang AY, Sea MM, Ho ZS, et al. Evaluation of handgrip strength as a nutritional marker and prognostic indicator in peritoneal dialysis patients. Am J Clin Nutr. 2005;81:79 – 86. 1252 f Physical Therapy Volume 91 31 Bohannon RW, Smith J, Hull D, et al. Deficits in lower extremity muscle and gait performance among renal transplant candidates. Arch Phys Med Rehabil. 1995;76: 547–551. 32 Ries JD, Echternach JL, Nof L, Gagnon Blodgett M. Test-retest reliability and minimal detectable change scores for the Timed “Up & Go” Test, the Six-Minute Walk Test, and gait speed in people with Alzheimer disease. Phys Ther. 2009;89: 569 –579. 33 García García M, Griñó Boira JM. Tratamiento sustitutivo de la función renal. In: Farreras Valentí P, Rozman C, eds. Medicina Interna. 13th ed. Madrid, Spain: Mosby-Doyma; 1995:892– 896. 34 Whitney SL, Wrisley DM, Marchetti GF, et al. Clinical measurement of sit-to-stand performance in people with balance disorders: validity of data for the Five-TimesSit-to-Stand Test. Phys Ther. 2005;85: 1034 –1045. 35 Csuka M, McCarty DJ. Simple method for measurement of lower extremity muscle strength. Am J Med. 1985;78:77– 81. 36 Cho BL, Scarpace D, Alexander NB. Tests of stepping as indicators of mobility, balance, and fall risk in balance-impaired older adults. J Am Geriatr Soc. 2004;52: 1168 –1173. 37 Macdonald JH, Marcora SM, Jibani M, et al. Intradialytic exercise as anabolic therapy in haemodialysis patients: a pilot study. Clin Physiol Funct Imaging. 2005;25: 113–118. 38 Ritchie C, Trost SG, Brown W, Armit C. Reliability and validity of physical fitness field tests for adults aged 55 to 70 years. J Sci Med Sport. 2005;8:61–70. 39 Li AM, Yin J, Yu CC, et al. The six-minute walk test in healthy children: reliability and validity. Eur Respir J. 2005;25: 1057–1060. 40 ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories. ATS statement: guidelines for the sixminute walk test. Am J Respir Crit Care Med. 2002;166:111–117. 41 Sekir U, Yildiz Y, Hazneci B, et al. Reliability of a functional test battery evaluating functionality, proprioception, and strength in recreational athletes with functional ankle instability. Eur J Phys Rehabil Med. 2008;44:407– 415. 42 Lunsford BR, Perry J. The standing heelrise test for ankle plantar flexion: criterion for normal. Phys Ther. 1995;75:694 – 698. 43 Portney LG, Watkins MP. Foundations of Clinical Research: Applications to Practice. 2nd ed. Upper Saddle River, NJ: Prentice Hall Health; 2000. Number 8 44 Stratford PW. Getting more from the literature: estimating the standard error of measurement from reliability studies. Physiother Can. 2004;56:27–30. 45 Palombaro KM, Craik RL, Mangione KK, Tomlinson JD. Determining meaningful changes in gait speed after hip fracture. Phys Ther. 2006;86:809 – 816. 46 Steffen T, Seney M. Test-retest reliability and minimal detectable change on balance and ambulation tests, the 36-Item ShortForm Health Survey, and the Unified Parkinson Disease Rating Scale in people with parkinsonism. Phys Ther. 2008;88: 733–746. 47 Mangione KK, Craik RL, McCormick AA, et al. Detectable changes in physical performance measures in elderly African Americans. Phys Ther. 2010;90:921–927. 48 Lin SJ, Bose NH. Six-minute walk test in people with transtibial amputation. Arch Phys Med Rehabil. 2008;89:2354 –2359. 49 Maher CA, Williams MT, Olds TS. The sixminute walk test for children with cerebral palsy. Int J Rehabil Res. 2008;31: 185–188. 50 Smeets RJ, Hijdra HJ, Kester AD, et al. The usability of six physical performance tasks in a rehabilitation population with chronic low back pain. Clin Rehabil. 2006;20: 989 –997. 51 Cider A, Carlsson S, Arvidsson C, et al. Reliability of clinical muscular endurance tests in patients with chronic heart failure. Eur J Cardiovasc Nurs. 2006;5:122–126. 52 Peolsson A, Hedlund R, Oberg B. Intra- and inter-tester reliability and reference values for hand strength. J Rehabil Med. 2001; 33:36 – 41. 53 Heiwe S, Tollback A, Clyne N. Twelve weeks of exercise training increases muscle function and walking capacity in elderly predialysis patients and healthy subjects. Nephron. 2001;88:48 –56. 54 Mercer TH, Crawford C, Gleeson NP, Naish PF. Low-volume exercise rehabilitation improves functional capacity and selfreported functional status of dialysis patients. Am J Phys Med Rehabil. 2002; 81:162–167. 55 Balady GJ, Berra KA, Golding LA, et al. ACSM’s Guidelines for Exercise Testing and Prescription. 6th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2000. 56 van Lier AM, Payette H. Determinants of handgrip strength in free-living elderly at risk of malnutrition. Disabil Rehabil. 2003;25:1181–1186. 57 Jan MH, Chai HM, Lin YF, et al. Effects of age and sex on the results of an ankle plantar-flexor manual muscle test. Phys Ther. 2005;85:1078 –1084. August 2011 Research Report Development of a Scale to Assess Avoidance Behavior Due to a Fear of Falling: The Fear of Falling Avoidance Behavior Questionnaire Merrill R. Landers, Cortney Durand, D. Shalom Powell, Leland E. Dibble, Daniel L. Young Background. A history of falls or imbalance may lead to a fear of falling, which may lead to self-imposed avoidance of activity; this avoidance may stimulate a vicious cycle of deconditioning and subsequent falls. Objective. The purpose of this study was to develop a questionnaire that would quantify avoidance behavior due to a fear of falling. Design. This study consisted of 2 parts: questionnaire development and psychometric testing. Questionnaire development involved an expert panel and 39 residents of an assisted living facility. Sixty-three community-dwelling individuals with various health conditions participated in psychometric testing. Method. Questionnaire development included the evaluation of face and content validity and factor analysis of the initial questionnaire. The final result of questionnaire development was the Fear of Falling Avoidance Behavior Questionnaire (FFABQ). In order to determine its psychometric properties, reliability and construct validity were assessed through administration of the FFABQ to participants twice, 1 week apart, and comparison of the FFABQ with other questionnaires related to fear of falling, functional measures of balance and mobility, and daily activity levels using an activity monitor. Results. The FFABQ had good overall test-retest reliability (intraclass correlation coefficient⫽.812) and was found to differentiate between participants who were considered “fallers” (ie, at least one fall in the previous year) and those who were considered “nonfallers.” The FFABQ predicted time spent sitting or lying and endurance. Limitations. A relatively small number of people with a fear of falling were willing to participate. Conclusion. Results from this study offer evidence for the reliability and validity of the FFABQ and support the notion that the FFABQ measures avoidance behavior rather than balance confidence, self-efficacy, or fear. M.R. Landers, PT, DPT, OCS, Department of Physical Therapy, School of Allied Health Sciences, Division of Health Sciences, University of Nevada, Las Vegas, 4505 Maryland Pkwy, Box 453029, Las Vegas, NV 891543029 (USA). Address all correspondence to Dr Landers at: [email protected]. C. Durand, PT, DPT, Fernley Physical Therapy, Fernley, Nevada, and Department of Physical Therapy, School of Allied Health Sciences, Division of Health Sciences, University of Nevada, Las Vegas. D.S. Powell, PT, DPT, Department of Physical Therapy, School of Allied Health Sciences, Division of Health Sciences, University of Nevada, Las Vegas. L.E. Dibble, PT, PhD, ATC, Department of Physical Therapy, University of Utah, Salt Lake City, Utah. D.L. Young, PT, DPT, Department of Physical Therapy, School of Allied Health Sciences, Division of Health Sciences, University of Nevada, Las Vegas. [Landers MR, Durand C, Powell DS, et al. Development of a scale to assess avoidance behavior due to a fear of falling: the Fear of Falling Avoidance Behavior Questionnaire. Phys Ther. 2011;91: 1253–1265.] © 2011 American Physical Therapy Association Published Ahead of Print: June 23, 2011 Accepted: April 18, 2011 Submitted: September 10, 2010 Post a Rapid Response to this article at: ptjournal.apta.org August 2011 Volume 91 Number 8 Physical Therapy f 1253 Fear of Falling Avoidance Behavior Questionnaire I t has been reported that 28% to 35% of individuals 65 years of age and older will fall within a year’s time, exposing them to serious potential injury.1 Although injuries as a result of a fall can be significant,2–7 a fear of falling may be a more serious problem, as it may lead to restricted activity and mobility in elderly people.2,3,8 Research indicates 50% of the elderly population have a fear of falling after experiencing just one fall, and a quarter of these individuals describe avoiding some activity due to their fear.6 A fall, however, is not a prerequisite to the fear of falling or subsequent activity restriction.2,9 Howland et al2 reported 20% of individuals who had not recently experienced a fall were still somewhat or very afraid of falling. Therefore, “fallers” and “nonfallers” alike may have a fear of falling that may lead to inactivity and social isolation, which in turn could stimulate deconditioning, functional decline, and decreased quality of life.2,10 –14 Despite the availability of many balance impairment tools, balance confidence measures, and self-efficacy measures, there is a need for a practical, clinical tool that can help quantify the effect of fear of falling on activity and participation, as defined by the International Classification of Functioning, Disability and Health (ICF).15 The most commonly used self-perceived balance confidence and efficacy questionnaires—the Activities-specific Balance Confidence (ABC) Scale16 and the Falls Efficacy Scale (FES)17— appear to be adequate at measuring “confidence” and “self-efficacy,” respectively, with activities of daily living (ADL); however, both questionnaires fail to capture the downstream consequence (ie, activity limitation and participation restriction) that a lack of confidence or decreased self-efficacy has on performing functional tasks. Further1254 f Physical Therapy Volume 91 more, the ABC Scale and the FES do not assess whether this confidence translates into avoidance behavior. Instead, these questionnaires are focused on the ICF-defined personal factors rather than activity and participation. Research has indicated these fall-related instruments often are used beyond the scope of their original design to measure fear of falling.18 Although performancebased measures of balance, gait, and fall risk (ie, Berg Balance Scale [BBS],19 –22 Dynamic Gait Index [DGI],7,23–25 Timed “Up & Go” Test [TUG],7,22 Functional Reach Test [FRT],26 –28 and dynamic posturography29,30) are good at measuring different aspects of balance and fall risk, they fail to capture the role and influence that the fear of falling has on activity and participation. In addition, the use of fall incidence is not an adequate measure of avoidance behavior, as an individual may avoid activities out of fear without having had any falls.8 There are few survey instruments that measure the effect of fear of falling on activity. The Survey of Activities and Fear of Falling in the Elderly (SAFFE) is an interviewbased, 11-item survey instrument intended to differentiate individuals who restrict their activity because of fear of falling from those who do not restrict their activity but still have a fear of falling.31 Although no test-retest reliability was published for the original SAFFE measure, the authors did provide evidence for convergent validity of the SAFFE.31,32 Evidence for reliability and validity of the SAFFE has been found recently for individuals with Parkinson disease (PD).33 Deshpande et al34 found SAFFE scores indicating severe and moderate activity restriction due to a fear of falling to be an independent predictor of increasing independent ADL disability. On the other hand, Hotchkiss et al35 found that the SAFFE was unable to accurately pre- Number 8 dict frequency of falls, activity limitation, and frequency of leaving home. The FES was a better predictor of people who exhibited activity restriction compared with the SAFFE, even though the FES is not intended to measure activity restriction.34 Although the SAFFE instrument has items consistent with the ICF levels of activity and participation, it is a 6-page document that involves qualitative and quantitative components, making it less userfriendly as well as time-consuming to complete and score. The SAFFE was designed to be administered in a face-to-face interview and has been described by researchers as “too long and burdensome” to administer, making it less practical for clinicians and researchers.18,36 A modified version of the SAFFE (Modified Survey of Activities and Fear of Falling in the Elderly [mSAFFE]) is a 17-item scale directed at activity avoidance.37 It was designed to be a self-administered questionnaire, which would be more efficient and less time-consuming to administer, complete, and score than its predecessor. The mSAFFE was found to have satisfactory test-retest reliability (rho⫽.75), but no validity was reported.37 Moore and Ellis18 compared the SAFFE and mSAFFE and reported that the mSAFFE may be a more useful measure of fear of falling and its effects on activity restriction, but they concluded that more research is needed to support the measure prior to its use. The Geriatric Fear of Falling Measure (GFFM) was created as a quick and culturally relevant measure of fear of falling for community-dwelling older adults living in Taiwan.38 It comprises 3 subscales (psychosomatic symptoms, risk prevention, modifying behavior), with a total score of 15 points, that are intended to measure activity restriction.38 The GFFM has good test-retest reliability August 2011 Fear of Falling Avoidance Behavior Questionnaire (r⫽.88) but poor validity (r⫽.29) compared with the FES.38 However, generalizability also is an issue for the GFFM, as the authors acknowledged the data are limited to Taiwanese older adults and suggested reliability and validity should be investigated further.18,38 The body of research on these measures emphasizes the effect of fear-avoidance behaviors on mobility. However, given the existing methodological limitations, there is still a need for a convenient and reliable clinical tool that can be used on heterogenous populations to standardize avoidance behavior at the level of activity and participation. To address this need, we are proposing a new, practical self-assessment measurement tool, the Fear of Falling Avoidance-Behavior Questionnaire (FFABQ). The FFABQ quantifies avoidance behavior (activity limitation and participation restriction) related to the fear of falling. It was based on the fear-avoidance model of exaggerated pain perception presented by Lethem et al39 and Troup et al.40 This model is used to understand the psychogenic component of an individual’s condition that may cause avoidance of certain activities.41 The model explains that individuals learn through operant conditioning to fear situations or stimuli that cause harm or stress and, as a result, to avoid that situation or these stimuli.41 The premise for the FFABQ was that individuals with a fear of falling (secondary to a previous fall or awareness of the negative consequences of falling) would avoid activities that put them at a risk for a fall. Therefore, the FFABQ would capture the avoidance of activities that would result from a fear of falling. An important goal of this project was to create a tool that would aid the researcher and the clinician alike in quickly, quantitatively, and reliAugust 2011 ably assessing avoidance behavior (activity limitation and participation restriction) due to a fear of falling. The FFABQ was not intended to be used in isolation but as a complement to other balance assessment tools in creating a more complete picture of the effects that balance impairment and falls have on a patient’s life. The purposes of this study were to outline the development of this questionnaire and to examine its psychometric properties and validity, so that it may be used in conjunction with other measurement tools to help create a more complete picture of the influence that falls, fall-avoidance behavior, and balance deficits have on the individual’s life. Our specific hypothesis was that people with a history of falling would report more fearavoidance behavior. In addition, because we believe that the FFABQ measures a different but tangentially related construct compared with other commonly used clinical balance tests, we hypothesized that there would be moderate correlations with these other tests. Lastly, we expected the FFABQ to contribute a unique amount of the variation beyond what is accounted for by other scales with a similar construct. Method The overall design of the study involved 2 main components: (1) questionnaire development and (2) questionnaire psychometrics. Questionnaire development included face validity, content validity, and a pilot study analysis of the initial questionnaire. The goal of this phase was to improve the syntax and appropriateness of the individual items on the questionnaire by using an expert panel of physical therapists and patients with a history of falling. In addition, other questions or items that were not present in the questionnaire would be added if the item domain was missing or underrepresented. A secondary goal of the development was to remove items that were redundant or very similar to other items. Ultimately, this process would shape the questionnaire into a final iteration, which then would undergo psychometric testing. This testing would include analysis of the reliability and construct validity of the final questionnaire. The goal of this phase was to establish the psychometric properties of this questionnaire. All participants provided written informed consent prior to the study. Questionnaire Development: Face Validity, Content Validity, and Pilot Study Analysis Face and content validity of the original 21-item questionnaire, as conceptualized by its developers, were determined by a panel of 13 experts: 7 physical therapy educators (including 4 who have published research related to balance or falls), 1 physical therapist who was a generalist, 3 physical therapists whose specialty was balance, and 2 patients with a history of falling. In addition to being physical therapists, several of the panel members provided additional breadth and depth of expertise through their experiences in community-based programs for people with PD and with family members who had restricted their activity due to a fear of falling. They were asked to assess the overall face and content validity of the questionnaire through an assessment of the language and the relevance of each individual item. Each item was stated as follows: “Due to my fear of falling, I avoid . . . (activity or participation),” with the following anchors: completely disagree, disagree, unsure, agree, completely agree. Each statement was scored using a Likert-style, 5-point ordinal scale (0⫽completely disagree to 4⫽completely agree), resulting in a total possible score of 84 points. A higher score indicates Volume 91 Number 8 Physical Therapy f 1255 Fear of Falling Avoidance Behavior Questionnaire Table 1. International Classification of Functioning, Disability and Health (ICF) Information Matrix Domain Codes for Each of the Fear of Falling Avoidance Behavior Questionnaire Items Item No. Due to My Fear of Falling, I Avoid: Walking Walking (d450) 2 Lifting and carrying objects (eg, cup, child) Lifting and carrying objects (d430) 3 Going up and downstairs Walking (d450) Moving around (d455) Moving around in different locations (d460) 4 Walking on different surfaces (eg, grass, uneven ground) Walking (d450) 5 Walking in crowded places Walking (d450) Moving around in different locations (d460) 6 Walking in dimly lit, unfamiliar places Walking (d450) Products and technology for personal use in daily living (e115) 7 Leaving home Moving around in different locations (d460) 8 Getting in and out of a chair Changing basic body position (d410) 9 Showering or bathing Washing oneself (d510) 10 Exercise Looking after one’s health (d570) 11 Preparing meals (eg, planning, cooking, serving) Preparing meals (d630) 12 Doing housework (eg, cleaning, washing clothes) Doing housework (d640) 13 Work or volunteer work Remunerative employment (d850) Nonremunerative employment (d855) 14 Recreational and leisure activities (eg, play, sports, arts and culture, crafts, hobbies, socializing, traveling) Recreation and leisure (d920) greater activity limitation and participation restriction as a result of the fear of the falling. The initial version of the questionnaire was pilot tested on 39 residents of an assisted living facility (mean age⫽85.03 years, SD⫽5.1; 16 fallers, 23 nonfallers; 11 male, 28 female) to assess each of the items of the questionnaire with factor analysis. These individuals were recruited using convenience sampling and consented to participate in the study with institutional review board approval. Factor analysis was used to reduce the number of items of the questionnaire by identifying items that had high intercorrelations. Results from the expert panel and the factor analysis guided several changes to the questionnaire. Items that resulted in high intercorrelations were combined or eliminated. Based on the panel recommendations, several items were 1256 f ICF Information Matrix Domain Codes 1 Physical Therapy Volume 91 reworded to be more consistent with the domains of the ICF model of activity limitation and participation restriction (Tab. 1). Those items that were not consistent with ICF model domains were dropped from the questionnaire. The final version of the questionnaire (ie, the FFABQ) consisted of 14 items (Appendix) ranked using the same Likert-style, 5-point ordinal scale as described above, resulting in a total possible score of 56 points. A high score indicates greater activity limitation and participation restriction as a result of the fear of the falling. Questionnaire Psychometrics: Reliability and Construct Validity Participants. The goal of participant recruitment for this portion of the study was to achieve variability in the amount of fear of falling and avoidance behavior. Therefore, a heterogenous sample with rel- Number 8 atively equivalent populations of those with and without fear of falling was needed. In order to obtain this desired sample, individuals who were healthy (presumably without balance problems) as well as those with pathologies known to have a high prevalence of balance problems (eg, cerebrovascular accident [CVA], PD) were the target populations for recruitment. Subsequently, 63 individuals (23 men and 40 women) with a mean age of 72.2 years (SD⫽7.2, range⫽60 – 88) were recruited as a convenience sample through snowball sampling at local senior centers, physical therapy balance clinics, and various support groups (eg, PD support group, stroke support group) in Las Vegas, Nevada. The participants were English-speaking and communitydwelling individuals of 60 years of age or older. The Mini-Mental State Examination (MMSE) was used to August 2011 Fear of Falling Avoidance Behavior Questionnaire Table 2. Primary Fall Categories and Their Respective Health Conditions Total No. of Participants (%) Healthy Parkinson Disease Cerebrovascular Accident Diabetes Cardiovascular Diagnosis Faller 25 (39.7%) 8 7 8 1 1 Frequent faller 12 (19.0%) 3 3 5 0 1 Recent faller 11 (17.5%) 2 3 5 0 1 Injured faller 11 (17.5%) 5 3 2 0 1 Fall Category Table 3. Self-Perceived Balance Confidence and Self-Efficacy Questionnaires Standardized Scale Evidence for Reliability Construct No. of Items Activities-specific Balance Confidence Scale16 Self-administered assessment of confidence with balance during various activities of daily living 16 items, scores ranging from 0% (not confident) to 100% (very confident) r⫽.9216 Correlated with age, balance score, gait scores, mobility scores, and falls in the previous year63 Falls Efficacy Scale17 Self-administered assessment of self-efficacy in completing activities of daily living without falling 10 items, total scores ranging from 10 (very confident) to 100 (not confident) r⫽.7117 Correlated with age, balance score, gait scores, mobility scores, and falls in the previous year63 determine the level of cognition of the participants. Those with moderate cognitive impairment (⬍21 on the MMSE) were excluded.42,43 The participants’ primary health conditions were as follows: 25 were healthy, 16 had PD, 11 had a history of CVA, 6 had diabetes, and 5 had a cardiovascular diagnosis (eg, coronary artery bypass, angina). Nine individuals had secondary diagnoses (eg, diabetes), but had a primary diagnosis that was more pronounced (eg, CVA). Participants also were classified using their recollection of their fall history. Twenty-five individuals were classified as a faller, defined as an individual who had at least one unexplained event where he or she descended to the floor in the previous year (Tab. 2). Twelve individuals were classified as frequent fallers, defined as having had 2 or more falls in the previous year. Eleven individuals were classified as recent fallers, defined as having had a fall in the previous month. An injured faller was defined as an individual who sustained an injury from a fall that August 2011 required medical assistance in the previous year. Eleven individuals were classified as injured fallers. These categories of classification were not mutually exclusive; as a result, a participant may have been placed in more than one category (Tab. 2). Reliability. In order to determine test-retest reliability, the FFABQ was administered to 63 participants twice, approximately 1 week apart. The first administration of the FFABQ was timed to determine the average length for completion. Two individuals were not included in the reliability analysis because they experienced a fall during the testretest period. Minimal detectable change (MDC) was calculated based on the standard error of measurement (SEM) using the test-retest reliability statistic, where rxx⫽test-retest reliability44 – 46: SEM⫽baseline standard deviation ⫻ 公1 ⫺ rxx . Once the SEM was determined, the MDC at a 95% confidence level (MDC95) for the questionnaire was calculated by multiplying the SEM by 1.96 (representing 95% of the area under the Evidence for Validity curve of a normal distribution) and 1.41 (the square root of 2 to control for possible error associated with calculating the coefficient from 2 data sets [ie, test and retest]).44 Construct and convergent validity. Construct validity was assessed via known-groups analysis and convergent validity. The purpose of the known-groups analysis was to compare a known characteristic, related to the construct of interest, which would allow logical inferences about the validity of the measurement tool (ie, FFABQ). For this study, our known-groups characteristic was the dichotomous response (“yes” or “no”) of the participants regarding their fall history (ie, faller, frequent faller, recent faller, or injured faller) (Tab. 2). Independentsamples t tests were utilized to determine whether there was a difference between participants with a history of falling and those without a history of falling based on their FFABQ scores. It was presumed that those with a history of falling would have more avoidance behavior than those without a fall history. Volume 91 Number 8 Physical Therapy f 1257 Fear of Falling Avoidance Behavior Questionnaire Table 4. Performance-Based Balance Assessment Toolsa Standardized Scale a Construct No. of Items Evidence for Reliability Evidence for Validity Berg Balance Scale19 Clinician-rated assessment of balance tasks 14 tasks, total score 0 (greatest fall risk) to 56 (least fall risk) ICC⫽.9819,20 Validated for populations that had a cerebrovascular accident or Parkinson disease20,64 and to predict future falls65 Dynamic Gait Index25 Clinician-rated assessment of ability to modify gait under various conditions Eight tasks, total score ranging from 0 (greatest fall risk) to 24 (least fall risk) ICCⱖ.98324,66 Correlated with Berg Balance Scale, timed walking test, Timed “Up & Go” Test, and Activities-specific Balance Confidence Scale in chronic stroke (range⫽.68– .83)67 and to predict fall risk68 Sensory Organization Test Computerized posturography used to challenge the 3 sensory components of balance Composite score of 6 scenarios, ranging from 0 to 100 based on age and heightadjusted averages ICC⫽.6666 Able to predict individuals with 2 or more falls in the previous 6 mo with cutoff score of 3869 Limits of stability Computerized posturography used to assess how far individual can purposefully displace center of gravity for 8 seconds Five scores (reaction time, movement velocity, endpoint excursion, maximum excursion, and directional control) based on age and height-adjusted averages Movement time ICC (2,1)⫽.825 Path sway ICC (2,1)⫽.846 Distance error ICC (2,1)⫽.63270 Anterior displacement was correlated to the Sensory Organization Test composite score for fallers (r⫽.79, P⫽.006)30 Timed “Up & Go” Test7,22 A timed test of functional mobility Three components (standing up, walking, and sitting down) where longer than 30 seconds indicated dependence in mobility Intrarater and interrater r values ranging from .93 to .9971 Correlated with Functional Independence Measure (⫺.59 at P⬍.001) in older individuals,72 Tinetti balance measure scores r⫽⫺.55, Tinetti gait measure scores (r⫽⫺.53), and walking speed (r⫽.66) where longer performance times predicted fall occurrence and decline in performance of activities of daily living in communitydwelling older people71 Self-selected gait speed73 Timed comfortable walking pace over 10 m N/A ICC⫽.9574 Slow walking speed associated with a fear of falling75 ICC⫽intraclass correlation coefficient, N/A⫽not applicable. Convergent validity was evaluated by comparing the FFABQ with measures of the same or similar constructs as other balance assessments using correlational statistics (Pearson product moment correlations) and multiple regression analysis (stepwise entry). In this study, the FFABQ was compared with the following 3 categories of assessment tools: selfperceived balance confidence and 1258 f Physical Therapy Volume 91 self-efficacy questionnaires (Tab. 3), performance-based balance assessment tools (Tab. 4), and endurance and activity level measures (Tab. 5). Activity levels were measured using activPAL monitors,* which measured the number of hours each day a par* PAL Technologies Ltd, 141 St James Rd, Glasgow G4 0LT, United Kingdom. Number 8 ticipant spent sitting or lying down, standing upright, and stepping. The monitors also measured the number of times the individual transitioned from sitting to standing or vice versa (up/down transitions) and metabolic equivalent of tasks (METs) performed each day. The activPAL software estimates METs by taking commonly accepted MET values for the aforementioned tasks and August 2011 Fear of Falling Avoidance Behavior Questionnaire Table 5. Endurance and Activity Level Measuresa Standardized Scale a Construct No. of Items Evidence for Reliability Evidence for Validity Six-Minute Walk Test A functional walking endurance test where the individual walks as far as possible in 6 min N/A High intraclass correlation between trials for adults older than 60 years of age: trials 1 and 2 (.88⬍r⬍.94), trials 2 and 3 (.91⬍r⬍.97)76 Correlated with treadmill scores (r⫽.78) and functional ability76 Activity monitor61 A device that measures activity levels for a 1-wk period Five components: hours sitting or lying, hours standing, hours stepping, up/down transitions, and metabolic equivalent of tasks Interdevice reliability of step number and cadence: ICC (2,1)ⱖ.9961 Absolute percentage of error ⬍1% for outdoor ambulation, ⱕ2% for walking speeds of ⱕ0.67 m/s62 ICC⫽intraclass correlation coefficient, N/A⫽not applicable. applying them to the individual’s daily activity. These types of activity monitors have been used in the past as a measure of walking activity in patients with spinal cord injury and cerebral palsy.47,48 Activity levels, as measured by these monitors, are not a direct measurement of activities or participation; they are, however, an indirect indicator of more movement, which would occur if someone were active (eg, walking). In a general sense, this measurement would allow some logical inferences about whether someone was active (ie, low FFABQ scores) or not (ie, high FFABQ scores). Someone who has significant activity limitation or participation restriction may not be moving around very much and would logically register low activity levels on activity monitors. On the other hand, someone who is engaged in activities and participation may register high activity levels on the activity monitors. Participants were asked to wear the activity monitors for 7 days; however, only data from days 2 through 6 were included and averaged for use in analysis because on days 1 and 7 participants did not have the monitor for a full day. Results Reliability Overall test-retest reliability was .812 (95% confidence interval (CI)⫽ August 2011 Figure. Confidence interval distribution among varied fall history groups. FFABQ⫽Fear of Falling Avoidance Behavior Questionnaire. .706 –.883), with 90.9 seconds as the average time of completion for the FFABQ (mean⫽90.9 seconds, SD⫽49.5). The test-retest reliability for participants with neurological involvement (ie, cerebrovascular accident, PD) was good (intraclass correlation coefficient [ICC] (3,1)⫽ .751, 95% CI⫽.524 –.878). Likewise, good reliability was noted for those reporting no health conditions (ICC [3,1]⫽.798, 95% CI⫽.593–.905). Reliability was not analyzed for the other health conditions, as there were not enough participants for each of the diagnostic categories. The individual MDC95 was 14.69 scale points for the overall sample (95% CI⫽11.61–17.77). Volume 91 Number 8 Physical Therapy f 1259 Fear of Falling Avoidance Behavior Questionnaire Table 6. Correlation Statistics of the Fear of Falling Avoidance Behavior Questionnaire With Other Measures of Balance and Activity r r2 ⫺.678a .460 .558a .311 Berg Balance Scale ⫺.498a .248 Dynamic Gait Index ⫺.585 a .342 Self-selected gait speed ⫺.475a .226 Timed “Up & Go” Test a .279 ⫺.385a .148 .280b .078 Measure Self-perceived balance/fall confidence questionnaires Activities-specific Balance Confidence Scale Falls Efficacy Scale Performance-based balance assessment tools .528 Sensory Organization Test composite score Limits of stability Reaction time Movement velocity ⫺.295 b .087 Maximum excursion ⫺.285b .081 Endpoint excursion ⫺.238 .057 Directional control ⫺.200 .040 Six-Minute Walk Test ⫺.523a .274 Hours sitting or lying a Endurance and activity level measures a b .326 .106 Hours standing ⫺.214 .046 Hours stepping ⫺.420a .176 Steps per day ⫺.416a .173 Up/down ⫺.227 .052 Metabolic equivalent of task ⫺.431a .186 Correlation is significant at Pⱕ.01 (2-tailed). Correlation is significant at Pⱕ.05 (2-tailed). Known-Groups Validity Analysis There was a statistically significant difference between fallers (mean⫽ 17.48, SD⫽15.20, 95% CI⫽11.20 – 23.76) and nonfallers (mean⫽7.97, SD⫽8.28, 95% CI⫽5.25–10.70) on FFABQ scores (t[61]⫽2.860, P⫽.007; homogeneity violation, P⫽.005) (Figure). The number of falls in the previous year also correlated significantly with the FFABQ scores (r⫽.408, r2⫽.166). Likewise, there was a statistically significant difference between the frequent fallers (mean⫽23.83, SD⫽17.54, 95% CI⫽ 12.69 –34.98) and nonfrequent fallers (mean⫽8.90, SD⫽8.83, 95% CI⫽6.42–11.38) on the FFABQ 1260 f Physical Therapy Volume 91 (t[61]⫽2.864, P⫽.014; homogeneity violation, P⫽.013) (Figure). There also was a statistically significant difference between recent fallers (mean⫽24.55, SD⫽17.52, 95% CI⫽12.78 –36.31) and nonrecent fallers (mean⫽9.04, SD⫽9.07, 95% CI⫽6.51–11.56) (t[61]⫽2.856, P⫽ .015; homogeneity violation, P⫽ .008) (Figure). However, there was not a statistically significant difference between the injured fallers (mean⫽19.00, SD⫽17.70, 95% CI⫽ 7.11–30.89) and the noninjured fallers (mean⫽10.21, SD⫽10.49, 95% CI⫽7.29 –13.13) (t[61]⫽1.589, P⫽ Number 8 .139; homogeneity violation, P⫽ .001; power⫽10.8%). Convergent Validity Analysis Table 6 contains the correlational statistics for the relationships of the FFABQ to self-perceived balance and fall confidence questionnaires (ie, ABC Scale and FES), performance-based balance assessment measures (ie, BBS, DGI, selfselected gait speed, TUG, Sensory Organization Test [SOT], and limits of stability [LOS]), and endurance and activity level measures (ie, SixMinute Walk Test [6MWT] and activity monitor results). The FFABQ scores correlated moderately with the ABC Scale, FES, BBS, DGI, TUG, and 6MWT scores. No significant correlations were noted between the FFABQ and the LOS endpoint excursion, LOS directional control, daily hours standing, and daily up/down transitions. Multiple linear regression analyses were used to compare the predictive validity of the variables with the most similar theoretical concepts (ie, FFABQ, ABC Scale, and FES) on measures of endurance (ie, 6MWT) and daily physical activity (ie, sitting or lying, stepping, up/down transitions, and daily METs). The only variable that correlated significantly with sitting or lying was the FFABQ (b⫽.055, ⫽.326, t⫽2.692, P⫽.009). The FFABQ explained 9.2% of the variance of time spent sitting or lying (adjusted r2⫽.092). None of the variables entered into the regression predicted time spent standing. However, the ABC Scale did significantly predict stepping (b⫽.016, ⫽.476, t⫽4.229, P⬍.0005), explaining 21.4% of the variance (adjusted r2⫽.214). Likewise, the ABC Scale was the only variable that was entered into the final model for prediction of up/down transitions (b⫽.262, ⫽ .340, t⫽2.828, P⫽.006) and daily METs (b⫽.030, ⫽.435, t⫽3.773, P⬍ .0005), explaining 10.1% (adjusted August 2011 Fear of Falling Avoidance Behavior Questionnaire r2⫽.101) and 17.6% (adjusted r2⫽.176) of the variance, respectively. Both the ABC Scale (b⫽ 2.209, ⫽.345, t⫽2.413, P⫽.019) and the FFABQ (b⫽⫺3.194, ⫽⫺.290, t⫽2.030, P⫽.047) were found to be correlated significantly with distance on the 6MWT. The full model explained approximately 31.6% of the variance (adjusted r2⫽ .316), with the ABC Scale explaining 28.1% (adjusted r2⫽.281) and the FFABQ explaining an additional 3.5% of the variance over and above the ABC Scale. Without the ABC Scale entered into the analysis, the FFABQ explained 26.2% (adjusted r2⫽.262) of the variance in the 6MWT scores. Discussion The primary purpose of this study was to develop a questionnaire that would be a practical, self-assessment tool with sound psychometric properties for measuring avoidance behavior due to a fear of falling. Our results offer preliminary evidence for the reliability and validity of the FFABQ for the assessment of activity limitation and participation restriction due to a fear of falling in community-ambulating elderly people. In addition, these results suggest that the FFABQ may have utility as a complementary assessment tool with other balance assessment tools to help create a more complete picture of the influence that balance impairment and falling have on a patient’s life. The FFABQ was reliable for community-ambulating elderly people with different diagnoses. Therefore, we feel that it can be reasonably used with all patients who have normal cognition or only mild cognitive deficits and suspected avoidance behavior due to a fear of falling. Because of its good reliability and ease of use, as evidenced by the short average time of completion (approximating 1.5 minutes), it offers the clinician a quick, August 2011 consistent, and standardized assessment tool. In addition, with an MDC of 15 scale points, the therapist can be confident that a change in score beyond this value would be indicative of a significant increase or decrease in activity and participation. The validity of the FFABQ was supported by results from the knowngroups analysis of this study. Participants who were classified as fallers reported a greater amount of avoidance behavior, as measured by the FFABQ, compared with nonfallers. As previous research has indicated, people who have experienced a fall may restrict activities or situations that would put them at risk for falling.2,6,12 Frequent fallers (2 or more falls in the previous year) also reported more avoidance behavior than nonfrequent fallers (one fall or fewer in the previous year). This result is consistent with findings by Delbaere et al.49 In addition, the more often a person fell, the more fear-avoidance behavior was exhibited. Although the correlation between the number of falls and the FFABQ scores was in the low-moderate range (r⫽.408), these results suggest that there may be a dose-dependent relationship between falling and fear-avoidance behavior. Recent fallers, presumably because of a fresh memory from the proximity of the incident, also exhibited more avoidance behavior, as measured by the FFABQ. In addition, individuals classified as fallers, frequent fallers, or injured fallers may have increased anxiety from the fall or anxiety related to their unsteadiness. This anxiety may contribute to a vicious cycle involving fear of falling, activity and participation restriction, and vulnerability to future falls.50 We had hypothesized that individuals who had sustained an injury due to a fall would be more likely to restrict their activity. Despite the mean difference of 8.79 scale points on the FFABQ, this hypothesized outcome was not the case in the present study. In relation to current evidence, our findings add little to the inconsistent data from other studies on fall injuries and avoidance behavior. One study showed that individuals who restricted their activity were more likely to have a history of an injurious fall in the previous year,51 whereas other studies showed there was no association between activity restriction and a fall causing an injury.52,53 However, we cannot rule out the possibility of a type II error because this comparison was clearly underpowered at 10.8%. Self-perceived balance confidence and self-efficacy questionnaires (ie, ABC Scale and FES) were most strongly correlated with the FFABQ. These moderate correlations may have been due to the possible contributing roles of confidence and self-efficacy on performing activities.54,55 That is, if a person feels more confident and capable in completing an activity, he or she will perform that activity more often. Although the constructs of confidence and self-efficacy differ from that of fear-avoidance behavior, the correlations noted in our study suggest these constructs are similar or closely related. If the FFABQ was truly measuring the same construct as either the FES or the ABC Scale, we would have observed higher intercorrelations. Therefore, these results support the notion that the FFABQ measures avoidance behavior rather than balance confidence, selfefficacy, or fear. The FFABQ also was moderately correlated with many performancebased measures of balance, which supports previous research that associates activity limitation with decreased physical capacity.52,56,57 Volume 91 Number 8 Physical Therapy f 1261 Fear of Falling Avoidance Behavior Questionnaire This association is reasonable because people with high avoidance behavior due to a fear of falls would logically have had some balance dysfunction.58 The performance-based measures that had a greater dynamic component (ie, BBS, DGI, selfselected gait speed, and TUG) were most strongly correlated with FFABQ scores. The most logical explanation is that participants with more avoidance behavior (ie, high FFABQ scores) had poorer dynamic balance capabilities. This finding also may be a result of decreased dynamic activity caused by avoidance behavior that has been shown to cause slower times on physical performance tests (eg, walking rapidly for 6.096 m [20 ft], turning a circle, rising from a chair 3 times).51 Performance-based measures of balance with a more static component (ie, SOT and LOS) also were correlated with the FFABQ, but these correlations were considerably lower than the dynamic measure correlations. Delbaere et al49 found that fear of falling and avoidance behavior measured by the mSAFFE were related to a reduced forward displacement as measured by the LOS. However, these findings may be induced by the negative impact that fear may have on postural performance as opposed to actual deterioration of the postural control systems.59 The smaller correlations between the FFABQ and more static performance-based measures suggest the FFABQ may be better able to capture avoidance of more dynamic activities. Perhaps the most important finding of the present study is the correlation between the FFABQ and daily physical activity measured by the activity monitors. Our claim that the FFABQ quantifies avoidance behavior in terms of activity limitation and participation restriction should be reflected by a decrease in daily 1262 f Physical Therapy Volume 91 physical activity. In addition, a decrease in physical activity, logically, can result in the downstream consequence of physical deconditioning and decreased endurance. The 6MWT was used in this study with this in mind. A positive correlation of the FFABQ with hours spent sitting or lying and negative correlations of the FFABQ with hours stepping, METs, and the 6MWT in the present study support the notion that individuals with high FFABQ scores (ie, high avoidance behavior) are less physically active (as measured by the activity monitor) and have decreased physical endurance (as measured by the 6MWT). This decrease in physical endurance may be the result of avoidance of mobility tasks, such as walking, which has been found to be more frequently avoided by elderly people with a fear of falling.49 However, hours spent standing, as measured by the activity monitor, was not correlated with the FFABQ. Because standing is a static and somewhat less mobile task, this would presumably not be considered a “risky” behavior. Therefore, static standing is not avoided as much as dynamic movements. This finding is consistent with the higher correlations of the FFABQ with dynamic balance measures compared with static balance measures. In addition, the transition from sitting to standing was not correlated with the FFABQ. This finding may be due to the requirement of this transition in unavoidable ADL tasks (eg, toileting, dressing, bathing) that often must be performed on a regular basis despite the presence of a fear of falling. Predictive validity was best represented by the FFABQ and ABC Scale. The FFABQ was the only variable that predicted hours spent sitting, a sedentary activity. The ability to predict this sedentary activity further supports the FFABQ’s capacity to measure activity limitation, as indi- Number 8 viduals with a high FFABQ score could reasonably be expected to engage in increased hours of sitting (ie, avoidance behavior). The ABC Scale was found to be a better predictor of activity levels compared with the FFABQ and FES. Previous research has shown the ABC Scale to be superior to the FES at differentiating between individuals who had a fear of falling and limited activity and those who did not.60 The FFABQ and ABC Scale both predicted endurance as measured by the distance walked on the 6MWT, indicating both tests may have the ability to predict the deconditioning that can occur after a substantial period of activity limitation. Although the ABC Scale predicted more of the variance of endurance, the FFABQ predicted an additional unique contribution over and above the ABC Scale, supporting the notion that the measurement constructs are related but different. Recruitment of community-ambulating elderly individuals who exhibited high fear-avoidance behavior was challenging. Those with high fear-avoidance behavior were not likely to participate in a study that required them to travel and be physically active, both prerequisites to participation in our study. Subsequently, a sample of convenience was used, and because of the difficulty in recruiting individuals with high fear of falling, we tended to have participants at the lower end of the scale. Future research targeting homebound elderly people may yield a participant pool with a higher level of fear-avoidance behavior. Another limitation of this study was the activPAL activity monitors. They could not be worn while swimming, and a couple of individuals participated in swimming during the week they wore the activity monitor. In addition, the combination of the activity monitor applied to the mid-thigh with adhesive backAugust 2011 Fear of Falling Avoidance Behavior Questionnaire ing resulted in frequent need for reapplication of the adhesive backing and in a lack of adherence to use of the activity monitor in a few cases. It has been reported that activity monitors are not sensitive to people who have a bradykinetic gait (ie, individuals with PD).61 For this reason, the activity monitor is not recommended for those with a selfselected gait speed below 0.67 m/s.62 However, in our study, the average gait speed of participants with PD was 1.23 m/s, making it unlikely that this was an issue. Conclusion The results from this study provide evidence for the reliability and validity of the FFABQ for different populations, including elderly people who are healthy and people with PD and CVA. Furthermore, our results support the notion that the FFABQ measures avoidance behavior rather than balance confidence, selfefficacy, or fear. The results of this study also illustrate that the FFABQ has the potential to offer the clinician an efficient way to assess the effectiveness of balance treatment on a patient whose fear of falling has triggered a reduction in his or her daily activity and participation. Currently, there are no other assessment tools that measure these sequelae of balance impairment and falls in a clinically useful and practical manner. All authors provided concept/idea/research design and writing. Dr Landers, Dr Durand, and Dr Powell provided data collection and analysis. Dr Landers provided project management, facilities/equipment, and institutional liaisons. Dr Powell provided participants. Dr Durand, Dr Powell, Dr Dibble, and Dr Young provided consultation (including review of manuscript before submission). This study was approved by the University of Nevada, Las Vegas, Biomedical Sciences Institutional Review Board. This research was presented at the Combined Sections Meeting of the American August 2011 Physical Therapy Association; February 9 –12, 2011; New Orleans, Louisiana. DOI: 10.2522/ptj.20100304 References 1 Masud T, Morris RO. Epidemiology of falls. Age Ageing. 2001;30(suppl 4):3–7. 2 Howland J, Peterson EW, Levin WC, et al. Fear of falling among the communitydwelling elderly. J Aging Health. 1993;5: 229 –243. 3 Hatch J, Gill-Body KM, Portney LG. Determinants of balance confidence in community-dwelling elderly people. Phys Ther. 2003;83:1072–1079. 4 King MB, Tinetti ME. Falls in communitydwelling older persons. J Am Geriatr Soc. 1995;43:1146 –1154. 5 Tinetti ME, Williams CS. 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Philadelphia, PA: Lippincott Williams & Wilkins; 2007. 24 McConvey J, Bennett SE. Reliability of the dynamic gait index in individuals with multiple sclerosis. Arch Phys Med Rehabil. 2005;86:130 –133. 25 Chiu Y, Fritz SL, Light KE, Velozo CA. Use of item response analysis to investigate measurement properties and clinical validity of data for the dynamic gait index. Phys Ther. 2006;86:778 –787. 26 Duncan PW, Weiner DK, Chandler J, Studenski S. Functional reach: a new clinical measure of balance. J Gerontol. 1990; 45:M192–M197. 27 Duncan PW, Studenski S, Chandler J, Prescott B. Functional reach: predictive validity in a sample of elderly male veterans. J Gerontol. 1992;47:M93–M98. 28 Weiner DK, Duncan PW, Chandler J, Studenski SA. Functional reach: a marker of physical frailty. J Am Geriatr Soc. 1992; 40:203–207. 29 Clark S, Rose DJ, Fujimoto K. Generalizability of the limits of stability test in the evaluation of dynamic balance among older adults. Arch Phys Med Rehabil. 1997;78:1078 –1084. 30 Wallmann HW. Comparison of elderly nonfallers and fallers on performance measures of functional reach, sensory organization, and limits of stability. J Gerontol A Biol Sci Med Sci. 2001;56:M580 –M583. 31 Lachman ME, Howland J, Tennstedt S, et al. Fear of falling and activity restriction: the Survey of Activities and Fear of Falling in the Elderly (SAFE). J Gerontol B Psychol Sci Soc Sci. 1998;53:P43–P50. 32 Jørstad EC, Hauer K, Becker C, et al. Measuring the psychological outcomes of falling: a systematic review. J Am Geriatr Soc. 2005;53:501–510. Volume 91 Number 8 Physical Therapy f 1263 Fear of Falling Avoidance Behavior Questionnaire 33 Nilsson MH, Drake AM, Hagell P. Assessment of fall-related self-efficacy and activity avoidance in people with Parkinson’s disease. BMC Geriatr. 2010;10:78. 34 Deshpande N, Metter EJ, Lauretani F, et al. Activity restriction induced by fear of falling and objective and subjective measures of physical function: a prospective cohort study. J Am Geriatr Soc. 2008;56: 615– 620. 35 Hotchkiss A, Fisher A, Robertson R, et al. Convergent and predictive validity of three scales related to falls in the elderly. Am J Occup Ther. 2004;58:100 –103. 36 Lamb SE, Jørstad-Stein EC, Hauer K, et al. Development of a common outcome data set for fall injury prevention trials: the Prevention of Falls Network Europe consensus. J Am Geriatr Soc. 2005;53: 1618 –1622. 37 Yardley L, Smith H. A prospective study of the relationship between feared consequences of falling and avoidance of activity in community-living older people. Gerontologist. 2002;42:17–23. 38 Huang TT. Geriatric fear of falling measure: development and psychometric testing. Int J Nurs Stud. 2006;43:357–365. 39 Lethem J, Slade PD, Troup JD, Bentley G. Outline of a fear-avoidance model of exaggerated pain perception: I. Behav Res Ther. 1983;21:401– 408. 40 Troup JD, Foreman TK, Baxter CE, Brown D. 1987 Volvo award in clinical sciences: the perception of back pain and the role of psychophysical tests of lifting capacity. Spine (Phila PA 1976). 1987;12:645– 657. 41 Slade PD, Troup JD, Lethem J, Bentley G. The fear-avoidance model of exaggerated pain perception: II. Behav Res Ther. 1983; 21:409 – 416. 42 Folstein MF, Folstein SE, McHugh PR. “Mini-mental state”: a practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12: 189 –198. 43 Mungas D. In-office mental status testing: a practical guide. Geriatrics. 1991;46:54 – 58, 63, 66. 44 Beaton DE, Bombardier C, Katz JN, Wright JG. A taxonomy for responsiveness. J Clin Epidemiol. 2001;54:1204 –1217. 45 Simonsick EM, Newman AB, Nevitt MC, et al. Measuring higher level physical function in well-functioning older adults: expanding familiar approaches in the health ABC study. J Gerontol A Biol Sci Med Sci. 2001;56:M644 –M649. 46 Faber MJ, Bosscher RJ, van Wieringen PC. Clinimetric properties of the performanceoriented mobility assessment. Phys Ther. 2006;86:944 –954. 47 Bowden MG, Hannold EM, Nair PM, et al. Beyond gait speed: a case report of a multidimensional approach to locomotor rehabilitation outcomes in incomplete spinal cord injury. J Neurol Phys Ther. 2008; 32:129 –138. 1264 f Physical Therapy Volume 91 48 Kuo YL, Culhane KM, Thomason P, et al. Measuring distance walked and step count in children with cerebral palsy: an evaluation of two portable activity monitors. Gait Posture. 2009;29:304 –310. 49 Delbaere K, Crombez G, Vanderstraeten G, et al. Fear-related avoidance of activities, falls and physical frailty: a prospective community-based cohort study. Age Ageing. 2004;33:368 –373. 50 Yardley L. Fear of falling: links between imbalance and anxiety. Rev Clin Gerontol. 2004;13:195–201. 51 Murphy SL, Williams CS, Gill TM. Characteristics associated with fear of falling and activity restriction in community-living older persons. J Am Geriatr Soc. 2002;50: 516 –520. 52 Howland J, Lachman ME, Peterson EW, et al. Covariates of fear of falling and associated activity curtailment. Gerontologist. 1998;38:549 –555. 53 Boyd R, Stevens JA. Falls and fear of falling: burden, beliefs and behaviours. Age Ageing. 2009;38:423– 428. 54 Bandura A. Self-efficacy mechanism in human agency. Am Psychol. 1982;37: 122–147. 55 Talley KM, Wyman JF, Gross CR. Psychometric properties of the Activities-specific Balance Confidence Scale and the Survey of Activities and Fear of Falling in older women. J Am Geriatr Soc. 2008;56: 328 –333. 56 Gill TM, Williams CS, Tinetti ME. Assessing risk for the onset of functional dependence among older adults: the role of physical performance [erratum in: J Am Geriatr Soc. 1995;43:1172]. J Am Geriatr Soc. 1995;43:603– 609. 57 Hindmarsh JJ, Estes EH Jr. Falls in older persons: causes and interventions. Arch Intern Med. 1989;149:2217–2222. 58 Tinetti ME, Mendes de Leon CF, Doucette JT, Baker DI. Fear of falling and fall-related efficacy in relationship to functioning among community-living elders. J Gerontol. 1994;49:M140 –M147. 59 Maki BE, Holliday PJ, Topper AK. Fear of falling and postural performance in the elderly. J Gerontol. 1991;46:M123–M131. 60 Myers AM, Powell LE, Maki BE, et al. Psychological indicators of balance confidence: relationship to actual and perceived abilities. J Gerontol A Biol Sci Med Sci. 1996;51:M37–M43. 61 Ryan CG, Grant PM, Tigbe WW, Granat MH. The validity and reliability of a novel activity monitor as a measure of walking. Br J Sports Med. 2006;40:779 –784. 62 Grant PM, Dall PM, Mitchell SL, Granat MH. Activity-monitor accuracy in measuring step number and cadence in community-dwelling older adults. J Aging Phys Act. 2008;16:201–214. 63 Huang TT, Wang WS. Comparison of three established measures of fear of falling in community-dwelling older adults: psychometric testing. Int J Nurs Stud. 2009;46: 1313–1319. Number 8 64 Blum L, Korner-Bitensky N. Usefulness of the Berg Balance Scale in stroke rehabilitation: a systematic review. Phys Ther. 2008;88:559 –566. 65 Muir SW, Berg K, Chesworth B, Speechley M. Use of the Berg Balance Scale for predicting multiple falls in communitydwelling elderly people: a prospective study. Phys Ther. 2008;88:449 – 459. 66 Ford-Smith CD, Wyman JF, Elswick RK Jr, et al. Test-retest reliability of the sensory organization test in noninstitutionalized older adults. Arch Phys Med Rehabil. 1995;76:77– 81. 67 Jonsdottir J, Cattaneo D. Reliability and validity of the dynamic gait index in persons with chronic stroke. Arch Phys Med Rehabil. 2007;88:1410 –1415. 68 Shumway-Cook A, Gruber W, Baldwin M, Liao S. The effect of multidimensional exercises on balance, mobility, and fall risk in community-dwelling older adults. Phys Ther. 1997;77:46 –57. 69 Whitney SL, Marchetti GF, Schade AI. The relationship between falls history and computerized dynamic posturography in persons with balance and vestibular disorders. Arch Phys Med Rehabil. 2006;87: 402– 407. 70 Newstead AH, Hinman MR, Tomberlin JA. Reliability of the Berg Balance Scale and Balance Master Limits of Stability Test for individuals with brain injury. J Neurol Phys Ther. 2005;29:18 –23. 71 Lin MR, Hwang HF, Hu MH, et al. Psychometric comparisons of the timed up and go, one-leg stand, functional reach, and Tinetti balance measures in communitydwelling older people. J Am Geriatr Soc. 2004;52:1343–1348. 72 Brooks D, Davis AM, Naglie G. Validity of 3 physical performance measures in inpatient geriatric rehabilitation. Arch Phys Med Rehabil. 2006;87:105–110. 73 Montero-Odasso M, Schapira M, Soriano ER, et al. Gait velocity as a single predictor of adverse events in healthy seniors aged 75 years and older. J Gerontol A Biol Sci Med Sci. 2005;60:1304 –1309. 74 Marchetti GF, Whitney SL, Blatt PJ, et al. Temporal and spatial characteristics of gait during performance of the Dynamic Gait Index in people with and people without balance or vestibular disorders. Phys Ther. 2008;88:640 – 651. 75 Kressig RW, Wolf SL, Sattin RW, et al. Associations of demographic, functional, and behavioral characteristics with activity-related fear of falling among older adults transitioning to frailty. J Am Geriatr Soc. 2001;49:1456 –1462. 76 Rikli RE, Jones CJ. The reliability and validity of a 6-minute walk test as a measure of physical endurance in older adults. J Aging Phys Act. 1998;6:363–375. August 2011 Fear of Falling Avoidance Behavior Questionnaire Appendix. Fear of Falling Avoidance-Behavior Questionnairea Name: Date: Please answer the following questions that are related to your balance. For each statement, please check one box to say how the fear of falling has or has not affected you. If you do not currently do the activities in question, try and imagine how your fear of falling would affect your participation in these activities. If you normally use a walking aid to do these activities or hold on to someone, rate how your fear of falling would affect you as if you were not using these supports. If you have questions about answering any of these statements, please ask the questionnaire administrator. Please check one box for each question Completely disagree (0) Disagree (1) Unsure (2) Agree (3) Completely agree (4) 1. Walking 䡺 䡺 䡺 䡺 䡺 2. Lifting and carrying objects (eg, cup, child) 䡺 䡺 䡺 䡺 䡺 3. Going up and downstairs 䡺 䡺 䡺 䡺 䡺 4. Walking on different surfaces (eg, grass, uneven ground) 䡺 䡺 䡺 䡺 䡺 5. Walking in crowded places 䡺 䡺 䡺 䡺 䡺 6. Walking in dimly lit, unfamiliar places 䡺 䡺 䡺 䡺 䡺 7. Leaving home 䡺 䡺 䡺 䡺 䡺 8. Getting in and out of a chair 䡺 䡺 䡺 䡺 䡺 9. Showering or bathing Due to my fear of falling, I avoid . . . 䡺 䡺 䡺 䡺 䡺 10. Exercise 䡺 䡺 䡺 䡺 䡺 11. Preparing meals (eg, planning, cooking, serving) 䡺 䡺 䡺 䡺 䡺 12. Doing housework (eg, cleaning, washing clothes) 䡺 䡺 䡺 䡺 䡺 13. Work or volunteer work 䡺 䡺 䡺 䡺 䡺 14. Recreational and leisure activities (eg, play, sports, arts and culture, crafts, hobbies, socializing, traveling) 䡺 䡺 䡺 䡺 䡺 Please make sure you have checked one box for each question. Thank you! Total: a /56 The Fear of Falling Avoidance-Behavior Questionnaire may not be used or reproduced without written permission from the authors. August 2011 Volume 91 Number 8 Physical Therapy f 1265 Case Report A Patient With Internal Carotid Artery Dissection Gilbert M. Willett, Neal A. Wachholtz G.M. Willett, PT, PhD, OCS, CSCS, Division of Physical Therapy Education, University of Nebraska Medical Center, 984420 Nebraska Medical Center, Omaha, NE 68198-4420 (USA). Address all correspondence to Dr Willett at: [email protected]. N.A. Wachholtz, PT, Excel Physical Therapy, Omaha, Nebraska. [Willett GM, Wachholtz NA. A patient with internal carotid artery dissection. Phys Ther. 2011;91: 1266 –1274.] © 2011 American Physical Therapy Association Published Ahead of Print: June 23, 2011 Accepted: April 26, 2011 Submitted: June 29, 2010 Background and Purpose. The purpose of this case report is to raise physical therapist awareness of Horner syndrome as a “red flag” for immediate medical referral. Case Description. A 45-year-old man sought physical therapy for examination and treatment of neck pain and headache symptoms 5 days after experiencing a whiplash-type injury while waterskiing. His complaints were similar to a prior condition diagnosed as occipital neuralgia that had successfully responded to education, cervical and thoracic joint mobilization, and exercise provided by a physical therapist. The initial examination findings also were similar to those of the previous episode. However, signs consistent with Horner syndrome were noted on the second visit. This finding raised immediate concern on the part of the treating clinician and resulted in prompt physician referral, medical diagnosis, and intervention. Outcomes. A magnetic resonance imaging angiogram revealed an internal carotid artery dissection. A successful outcome was achieved over the course of 6 months through medical intervention, which consisted of anticoagulant therapy and modification of activity levels. Discussion. In this case, the patient’s sudden onset of signs of Horner syndrome was indicative of a medical emergency—internal carotid artery dissection. Post a Rapid Response to this article at: ptjournal.apta.org 1266 f Physical Therapy Volume 91 Number 8 August 2011 Internal Carotid Artery Dissection I ndividuals with neck pain and headaches commonly seek physical therapy intervention for their symptoms. Neck pain is second only to low back pain as a significant cause of impairment.1 The reported 12-month prevalence of neck pain varies from 30% to 50%, and lifetime prevalence is approximately 70%.1 Fifteen percent of visits to hospitalbased physical therapists are neck pain related.1 Individuals with neck pain and headaches commonly demonstrate impairments that appear to be associated with their symptomatic complaints. Forward head posture has been linked to neck pain and headache symptoms.2,3 Upper cervical spine joint disorders are directly associated with cervicogenic headache.4 – 6 Weakness of the longus colli and longus capitis cervical spine muscles also have been linked to neck pain and headaches.7–9 Common problems associated with traumatic, whiplash-type injuries include neck pain, occipital headaches, and greater occipital neuralgia.10,11 Individuals with whiplash-type injuries often demonstrate elements of all of these impairments upon initial examination. Patients should be continuously monitored for new signs or symptoms, which would raise “red flags” relative to appropriateness for physical therapy intervention.12 A patient who suddenly develops signs of Horner syndrome, which include ptosis (drooping eyelid) and miosis (pupil constriction) of one eye, would be one example of a new finding indicative of a need for further medical evaluation. Physical therapists need to be able to make decisions regarding the need for medical referral based on patient observation and examination findings.13 cervical ganglion. Next, it ascends within the adventitia of the internal carotid artery. Sympathetic nerve fibers join the ophthalmic division of the fifth cranial nerve (trigeminal nerve) in the cavernous sinus and travel with it to the orbit. These sympathetic fibers innervate the iris dilator muscle as well as Müller’s muscle, a small smooth muscle in the eyelids responsible for a minor portion of the upper lid elevation and lower lid retraction.14 A plethora of medical conditions can cause Horner syndrome, a number of which require immediate medical examination.15 Some of the most common causes of Horner syndrome reported in the literature include surgical trauma, cervical carotid artery dissection, and a cavernous sinus mass.16 Horner syndrome can result from a lesion occurring along the sympathetic nervous system pathway. The pathway starts in the hypothalamus area of the brain and travels along the sympathetic trunk to the superior The patient stated that his recurrence of symptoms (similar to his visit 2 years previously) was precipitated by a “major wipeout” while waterskiing on a Saturday afternoon (5 days prior to the examination by August 2011 The purpose of this case report is to increase physical therapist awareness of signs of Horner syndrome that may indicate a potentially catastrophic underlying medical condition. the physical therapist). He stated he caught the edge of his slalom ski while cutting across the water, which resulted in a “face plant” into the water. He estimated the boat speed at around 50 km/hr. He reported having a global headache the same day and taking ibuprofen to reduce his symptoms. He stated that the symptoms subsided the following day, and he returned to his regular work duties as a physical therapist (with more than 20 years of practice) with no limitations. He reported the onset of a primarily right-sided, severe headache and neck pain 4 days after the initial trauma. He sought physical therapy the day after the onset of this headache. This self-referral was to a therapist who worked for another employer but knew the patient well and had treated him previously. Verbal questioning to screen for general health and constitutional symptoms revealed no significant findings.17 Specific questions included: • What medical conditions have you been diagnosed with? • What issues have you seen your physician for in the previous 5 to 10 years? • What surgeries have you had? • Have you experienced any constitutional symptoms such as fever, dizziness, nausea, trouble swallowing, headaches, or numbness and tingling in the previous 2 weeks? Case Description: Details of the Risk Management Topic The patient was a 45-year-old man who reported cervical pain (greater on the right side than on the left side) and a primarily right-sided headache extending from the occipital region to just above the eye (Fig. 1). He had been treated successfully 2 years previously by the same physical therapist for a similar complaint. His medical diagnosis at the time had been “occipital neuralgia” of unknown onset. This diagnosis had been made by an anesthesiologist/ pain specialist. The patient had been referred to by his family physician. The only medical care the patient had received in the previous 5 years was for occipital neuralgia, as previously reported. No prior history of surgery or use of prescribed medications was reported. The patient noted the constant, stabbing headache and neck pain on his right side as being significant, while stating that the mild ache on the left side of his head and neck felt as though it may be resultant from the pain on the right. He also reported that the Volume 91 Number 8 Physical Therapy f 1267 Internal Carotid Artery Dissection in the clinical setting to measure a patient’s self-reported function. Although this scale has not been validated specifically in patients with headache or neck pain, it has shown a strong correlation with wellestablished outcome measures for the shoulder.19 Figure 1. Pain diagram completed by the patient during the initial examination. back of his head was tender to touch on the right side. The body chart pain diagram completed by the patient is shown in Figure 1. The patient was asked to rate his pain on the right and left sides using a numeric pain rating scale (NPRS), an 11-point scale with 0 indicating “no pain” and 10 indicating “worst pain imaginable.” Changes in pain intensity have been shown to be accurately measured using the NPRS.18 He rated his right-side worst pain over the previous 24 hours as 9/10, and as 7/10 at the time of the 1268 f Physical Therapy Volume 91 examination. He stated his “best” pain was 7/10 and his average pain was 7/10 as well. He rated his leftside worst and best pain over the previous 24 hours as 2/10, and his pain level remained at 2/10 at the time of the examination. The patient reported not experiencing any night pain or difficulty sleeping since the accident. A global function rating of 80% was identified by the patient, with 0% representing “unable to perform any activity” and 100% representing “able to perform all activities without limitation.” The global function rating scale is commonly used Number 8 Clinical Impression The patient’s primary concern was right-sided headache. Based on his medical history, the examining therapist wanted to discern whether the headache was possibly due to a re-aggravation of the postural and upper cervical and thoracic joint hypomobility issues encountered previously, or perhaps a non– musculoskeletal-related condition in need of additional medical evaluation. The objective of the physical examination was to assess whether musculoskeletal impairments that reproduced his headache symptoms were present. Upper cervical and thoracic joint mobility limitations and myofascial trigger points in the cervical region are commonly associated with cervicogenic headaches.3,20 The focus of the physical examination was on these areas. Additional medical history information that can be useful for differential screening of individuals with headaches includes: detailed assessment of neurologic symptoms (eg, seizures, confusion, changes in alertness, clumsiness), eye pain and simultaneous vision changes, and family history (migraines or cancer).20 The initial presentation of this patient suggested a relatively straightforward reoccurrence of his previous musculoskeletal dysfunction, based on the absence of any differential screening red flags. However, the subsequent onset of new symptoms at the second visit completely changed the course of intervention and prognosis of this case. August 2011 Internal Carotid Artery Dissection Physical Examination Posture Moderate forward head posture was noted upon observation of sitting and standing. Active Range of Motion Cervical spine active range of motion (AROM) and associated symptom responses were measured with the patient in a sitting position. An inclinometer was used to measure cervical flexion and extension, and cervical rotation was measured with a standard goniometer. The details of these measurement procedures have been described elsewhere, and the reliability findings have been reported as .84 for flexion and extension, .82 for side bending, and .81 for rotation.21–23 Cervical spine motion was as follows: flexion⫽50 degrees, extension⫽57 degrees, left rotation⫽63 degrees, right rotation⫽65 degrees, side bending to the left⫽33 degrees, and side bending to the right⫽35 degrees. Discomfort was noted at the end range of left rotation and left-side bending. Moderate limitations were noted during AROM assessment of C1/occipital flexion (3°) and C1–C2 left rotation (25°) with the patient in a sitting position. Joint Mobility Hypomobility was noted with posterior to anterior “spring” testing of the mid and upper thoracic spine (⫽⫺.2 to .26 depending on level tested) and with C1/occipital flexion (⫽.29) and C1–C2 left rotation assessments (⫽.20 left, .37 right). Mild reproduction of the patient’s symptoms was noted with assessment of the hypomobile regions of the cervical spine. Mobility assessment of the cervical and thoracic spine in patients with mechanical neck pain has been shown to have fair to poor reliability.23 August 2011 Neurologic Screen A neurologic screen (upper-limb and head/face sensation, muscle strength [force-generating capacity] and deep tendon reflexes) was performed. Findings were symmetrical and unremarkable for all areas tested. These tests have been described elsewhere.24 Numbness has been reported to have a sensitivity of .79 and a specificity of .25, weakness a sensitivity of .65 and a specificity of .39, and deep tendon reflexes a sensitivity ranging from .24 to .03 and a specificity ranging from .95 to .93.24 Special Tests Sharp-Purser test. The findings of this test for cervical instability were unremarkable. The details of this test have been described elsewhere and have been reported to have acceptable sensitivity (.69) and specificity (.96), a positive likelihood ratio of 17.25, and a negative likelihood ratio of 0.32.24 Vertebral artery test. No significant findings other than positionrelated discomfort were noted. This test was performed in the anticipation that the patient might benefit from grade 5 cervical spine manual therapy interventions as used in his previous treatment. The clinical utility of this test alone has been reported to be limited, and the use of a qualitative assessment of all vascular risk factors (carotid and vertebral) incorporating a “systems-based approach” has been recommended in order to enhance the clinical reasoning process.25 Palpation Muscle guarding and tightness were noted in the suboccipital region and were greater on the right side than on the left side. Headache symptoms were aggravated with palpation of both the suboccipital paraspinal musculature and occiput of the skull on the right side. Physical examination test reliability and diagnostic utility must be taken into consideration when selected as part of the examination procedure by the clinician. A thorough explanation and discussion of these issues are available elsewhere.24 The examination was concluded at this point due to irritability of the patient’s symptoms. Additional assessment of functional movements and cervical muscle strength would have been included in the examination provided the patient’s symptoms had not been aggravated. The patient’s increased discomfort from the examination prompted the therapist to reduce the aggressiveness of his planned initial manual therapy intervention strategy. The patient’s goals for physical therapy were to eliminate the symptoms and to review and modify his self-management home program, if needed. Clinical Impression Based on the patient’s uneventful return to normal activities for several days, the similarity of physical examination findings to the initial presentation 2 years previously, and headache symptoms and palpation findings being consistent with occipital neuralgia, the physical therapist hypothesized that the patient had exacerbated his previous condition.26,27 Occipital neuralgia pain is characterized as a constant “stabbing” and associated with tenderness to palpation of the occipital nerve.26 Occipital neuralgia has been cited as a common cause of cervicogenic headache.28 Clinical diagnosis is difficult because of the overlying features between primary headaches (eg, tension-type migraines) and cervicogenic headaches. Interventional pain physicians have focused on supporting the clinical diagnosis of cervicogenic headaches with confirmatory nerve blocks. There is mounting evidence that manual therapy interventions aimed at vertebral mobility Volume 91 Number 8 Physical Therapy f 1269 Internal Carotid Artery Dissection Figure 2. Photograph of the patient showing right-side ptosis (drooping eyelid) and miosis (pupil constriction). impairments can be effective in the management of occipital neuralgia when used in conjunction with medical management strategies such as occipital nerve block injections.20 The overall examination findings appeared to support the physical therapist’s initial hypothesis that the patient had a musculoskeletal impairment-based dysfunction that should be responsive to interventions aimed at addressing the impairments of joint hypomobility and muscle guarding and a potential need for modification of home exercises (to be assessed in future visits). The therapist decided that any soft tissue injuries that the patient may have incurred from the skiing acci- Figure 3. Magnetic resonance imaging angiogram of the patient demonstrating entire view of the carotid arteries (anterior-posterior view). The white arrow is pointing to the area of dissection of the right internal carotid artery; note the reduced blood flow (narrow area of contrast medium). 1270 f Physical Therapy Volume 91 Number 8 dent were most likely in the early proliferative phase of healing secondary to the traumatic incident and that initial interventions should not include aggressive cervical manual interventions (grade 4 or 5 mobilization) or resistance exercises at that time. Of note, decision rules for whether referral for cervical radiographs is appropriate in cases of cervical trauma are well documented in the literature.29 In this case, the patient’s uneventful return to work, lack of upper-limb symptoms, and cervical AROM measurements led the therapist to rule out the need for radiograph referral at the time of the initial examination. The initial interventions were based on the impairments noted in the examination. These interventions included review and practice of appropriate posture and head position in sitting and standing, supine upper thoracic (third thoracic vertebral level) anterior-posterior joint (grade 5) mobilization, gentle suboccipital manual traction and occipital release, and contract-relax mobilization (grades 2 and 3) for left rotation of C1–C2, followed by application of an ice pack on the cervical region. The manual therapy techniques used in this case are well described in the literature.20,30,31 The patient reported mild symptomatic relief at the end of the intervention and demonstrated symmetrical C1–C2 rotation mobility (⬃40°). The patient was instructed to perform seated or standing chin tuck exercises and cervical rotation AROM exercises within the pain-free range of motion throughout the following day. A return visit was scheduled for 2 days later. Upon his second visit for treatment (Saturday, 7 days after the initial injury), the patient reported a brief reduction in his headache (⬃2 hours) after the initial visit (5/10 on the NPRS), but his pain level had August 2011 Internal Carotid Artery Dissection returned to 7/10. Next, the therapist asked the patient to actively demonstrate his upper cervical (C1–C2) rotation by flexing his chin to his chest and rotating side to side. Observation of this AROM revealed symmetrical movement (⬃40° bilaterally), with no patient report of change in symptoms. When the patient looked up from the AROM assessment, the therapist noted pupil asymmetry with miosis on the right side and ptosis of the right eyelid (Fig. 2). The patient had not noticed these signs prior to the therapist bringing them to his attention. The therapist recognized the signs as being consistent with Horner syndrome. Horner syndrome can result from a wide range of medical conditions, including tumors, spinal cord injuries, vascular problems, and specific types of headaches.14 An appropriate medical evaluation and a timely elucidation of the etiology may allow for a potentially lifesaving intervention.14 No further assessment was performed. The therapist considered these signs as a red flag and informed the patient he wanted to contact his physician immediately to report this change in findings. The patient chose to contact his physician at the time via personal cell phone. If the patient had not chosen to contact his physician personally, the therapist would have called the patient’s family physician to describe the situation and ask for recommendations. In retrospect, after learning of the potential high-risk medical diagnoses associated with the sudden onset of signs of Horner syndrome, providing the patient with an immediate ride to the closest hospital emergency department would have been appropriate.11,31,32 Actions Taken to Address the Risk The patient’s physician ordered a head magnetic resonance imaging August 2011 Figure 4. Magnetic resonance imaging angiogram of the patient providing a cross-sectional view of the internal carotid arteries. The white arrow is pointing to the area of dissection of the right internal carotid artery; note the reduced blood flow (large area of lighter density of contrast medium and small area of greater density). (MRI) scan the same day. Negative findings and accompanying cervical pain led the physician to consider carotid artery dissection as a possible cause.12,14,33 The patient was sent to the emergency department of a local hospital for a neurologist consultation and a cervical MRI angiogram (MRA). The MRA images are shown in Figures 3 and 4. The findings resulted in a diagnosis of internal carotid artery dissection (ICAD). The patient was hospitalized, and treatment of vascular risk factors for stroke prevention with heparin was initiated. He was subsequently released from the hospital with ongoing anticoagulation therapy (Coumadin*) for 6 months and advised to limit physical activity to mild amounts of exertion. The goal of this standard approach to medical management of ICAD via pharmaceutical intervention is to reduce the possibility of a cerebrovascular accident.34 A follow-up MRA at the end of the treatment period (6 months later) revealed normal, symmetrical carotid artery findings (Fig. 5). The patient returned to full activity levels with no limitations. His neck pain and headaches had gradually receded over the 6-month treatment period, and he reported no symptoms 1 year later. The patient’s right pupil miosis and eyelid ptosis also diminished over the course of the 6 months, but remained observable to the trained eye. * Bristol-Myers Squibb Co, PO Box 4500, Princeton, NJ 08543-4500. Volume 91 Number 8 Physical Therapy f 1271 Internal Carotid Artery Dissection of Horner syndrome include dorsolateral medullary stroke and carotid artery dissection.12 In cases where the cause of Horner syndrome is unknown, patient signs and symptoms assist with localizing the area of the lesion and subsequent diagnosis of the causes. For example, acute neck or face pain indicate a lesion in the cervical region, arm pain or weakness indicate a lesion in the paraspinal region, and sixth cranial nerve palsy indicates a lesion in the cavernous sinus area.12 Figure 5. Follow-up magnetic resonance imaging angiogram of the patient (after 6 months of anticoagulant therapy) demonstrating entire view of the carotid arteries (anteriorposterior view). The white arrow is pointing to the area where the dissection of the right internal carotid artery had occurred. Discussion Internal carotid artery dissection occurs as a result of a tear in the inner lining of the artery. The tear can be spontaneous or associated with mild trauma such as sneezing or more severe trauma such as whiplash injury or aggressive cervical spine rotation manipulation.15,35– 40 Understanding of the pathophysiology that makes a person susceptible to ICAD is somewhat limited.41 The signs and symptoms experienced by the patient in this case report are similar to those described in other examples in medical literature.15,42– 45 occurs in adults at a mean age of 40 years and with a male:female ratio of 1.5.38 Approximately 60% of ICADs appear to occur spontaneously.44 The clinical presentation of spontaneous dissections of the internal carotid artery may include cervical or cranial pain, Horner syndrome, and cranial nerve palsy; however, ICAD also may be silent. The favorable natural history of ICAD emphasizes the need for a noninvasive approach to detection, monitoring, and follow-up. Follow-up studies suggest a fairly good overall prognosis in adults.38 Internal carotid artery dissection accounts for up to one fifth of ischemic strokes occurring in people under the age of 45 years. It typically The onset of signs consistent with Horner syndrome was the reason for concern on the part of the therapist in this case report. Common causes 1272 f Physical Therapy Volume 91 Number 8 Common signs and symptoms associated with any ICAD include ipsilateral clinical manifestations: head, facial, or neck pain; Horner syndrome; pulsatile tinnitus; and cranial nerve palsy.35 Cluster headache symptoms also have been associated with Horner syndrome signs and underlying ICAD.45– 48 The classic signs of Horner syndrome include: miosis, ptosis, and facial anhydrosis, all on the ipsilateral side of the head.12 Diagnostic imaging (MRI or angiography) is strongly recommended in cases where an individual has Horner syndrome of unknown etiology, especially when accompanied by head, face, or neck pain.12,16,49 Approximately 50% of individuals who have had a carotid artery dissection also have connective tissue aberrations of their skin.41 The patient in this case report did not have any medical history or physical findings that indicated he may have had a connective tissue disorder; however, he did exhibit signs and symptoms consistent with ICAD upon his second visit for physical therapy intervention. In conclusion, this case report describes a patient who initially presented a history, signs, and symptoms of what appeared to be a treatable musculoskeletal condition. The sudden onset of signs consistent with Horner syndrome in addition to his continued headache and August 2011 Internal Carotid Artery Dissection neck pain complaints prompted the attending physical therapist to immediately refer the individual to his physician. An ICAD was diagnosed, and appropriate medical treatment ensued. Identification of signs inconsistent with a musculoskeletal system injury facilitated the medical referral. In retrospect, the therapist could have considered more extensive cranial nerve and cervical testing during the initial examination due to the patient’s initial history, which included trauma. However, it is unlikely these examinations would have revealed additional information if the onset of his ICAD was spontaneous or if it developed gradually after the initial trauma. The therapist also may have put too much stock in the information and recommendations being provided by the patient due to his background and experience as a physical therapist. A thorough examination should always be conducted, regardless of a patient’s background and experience. The lesson learned: a sudden onset of signs atypical for what is expected (Horner syndrome for a musculoskeletal injury in this case) should be considered a red flag for medical referral. Dr Willett provided concept/idea/project design. Mr Wachholtz provided data collection. Both authors provided writing and consultation (including review of manuscript before submission). DOI: 10.2522/ptj.20100217 References 1 Gross AR, Haines T, Goldsmith CH, et al. Knowledge to action: a challenge for neck pain treatment. J Orthop Sports Phys Ther. 2009;39:351–363. 2 Silva AG, Punt TD, Sharples P, et al. Head posture and neck pain of chronic nontraumatic origin: a comparison between patients and pain-free persons. Arch Phys Med Rehabil. 2009;90:669 – 674. 3 Fernandez-de-Las-Penas C, Cuadrado ML, Pareja JA. Myofascial trigger points, neck mobility, and forward head posture in episodic tension-type headache. Headache. 2007;47:662– 672. August 2011 4 Ahn NU, Ahn UM, Ipsen B, An HS. Mechanical neck pain and cervicogenic headache. Neurosurgery. 2007;60(1 suppl 1): S21–S27. 5 Becker WJ. Cervicogenic headache: evidence that the neck is a pain generator. Headache. 2010;50:699 –705. 6 Biondi DM. Cervicogenic headache: a review of diagnostic and treatment strategies. J Am Osteopath Assoc. 2005;105(4 suppl 2):16S–22S. 7 Jull GA, Barrett C, Magee R, Ho P. Further clinical clarification of the muscle dysfunction in cervical headache. Cephalalgia. 1999;19:179 –185. 8 Jull GA, Kristjansson E, Dall’Alba P. Impairment in the cervical flexors: a comparison of whiplash and insidious onset neck pain patients. Man Ther. 2004;9:89 –94. 9 Jull GA, Falla D, Vicenzino B, Hodges PW. The effect of therapeutic exercise on activation of the deep cervical flexor muscles in people with chronic neck pain. Man Ther. 2009;14:696 –701. 10 Raisbeck CC. Chronic whiplash and whiplash-associated disorders: an evidencebased approach. J Am Acad Orthop Surg. 2008;16:121–122. 11 Yadla S, Ratliff JK, Harrop JS. Whiplash: diagnosis, treatment, and associated injuries. Curr Rev Musculoskelet Med. 2008; 1:65– 68. 12 Trobe JD. The evaluation of Horner syndrome. J Neuroophthalmol. 2010;30:1–2. 13 Jette DU, Ardleigh K, Chandler K, McShea L. Decision-making ability of physical therapists: physical therapy intervention or medical referral. Phys Ther. 2006;86: 1619 –1629. 14 Walton KA, Buono LM. Horner syndrome. Curr Opin Ophthalmol. 2003;14:357–363. 15 Bazari F, Hind M, Ong YE. Horner’s syndrome: not to be sneezed at. Lancet. 2010; 375:776. 16 Almog Y, Gepstein R, Kesler A. Diagnostic value of imaging in horner syndrome in adults. J Neuroophthalmol. 2010;30:7–11. 17 Goodman CC, Snyder TE. Differential Diagnosis in Physical Therapy. 3rd ed. Philadelphia, PA: WB Saunders Co; 2000. 18 Jensen MP, Turner JA, Romano JM. What is the maximum number of levels needed in pain intensity measurement? Pain. 1994; 58:387–392. 19 Williams GN, Gangel TJ, Arciero RA, et al. Comparison of the single assessment numeric evaluation method and two shoulder rating scales: outcomes measures after shoulder surgery. Am J Sports Med. 1999;27:214 –221. 20 Fernandez-de-las-Penas C, Arendt-Nielsen L, Gerwin RD. Tension-Type and Cervicogenic Headache. Sudbury, MA: Jones and Bartlett Publishers; 2010. 21 Childs JD, Cleland JA, Elliott JM, et al. Neck pain: clinical practice guidelines linked to the International Classification of Functioning, Disability and Health from the Orthopedic Section of the American Physical Therapy Association [erratum in: J Orthop Sports Phys Ther. 2009; 39:297]. J Orthop Sports Phys Ther. 2008; 38:A1–A34. 22 Cleland JA, Childs JD, Fritz JM, et al. Development of a clinical prediction rule for guiding treatment of a subgroup of patients with neck pain: use of thoracic spine manipulation, exercise, and patient education. Phys Ther. 2007;87:9 –23. 23 Cleland JA, Childs JD, Fritz JM, Whitman JM. Interrater reliability of the history and physical examination in patients with mechanical neck pain. Arch Phys Med Rehabil. 2006;87:1388 –1395. 24 Cleland J, Koppenhaver S, Netter FH. Netter’s Orthopaedic Clinical Examination: An Evidence-Based Approach. 2nd ed. Philadelphia, PA: Saunders/Elsevier; 2011: 561. 25 Kerry R, Taylor AJ, Mitchell J, McCarthy C. Cervical arterial dysfunction and manual therapy: a critical literature review to inform professional practice. Man Ther. 2008;13:278 –288. 26 Carayannopoulos AG. Teaching case: occipital neuralgia in a young patient. Headache. 2007;47:1367–1370. 27 Goicochea MT, Romero C, Leston JA. Occipital neuralgia with cervical myelitis. Cephalalgia. 2008;28:567–568. 28 Hoppenfeld JD. Cervical facet arthropathy and occipital neuralgia: headache culprits. Curr Pain Headache Rep. 2010;14: 418 – 423. 29 Stiell IG, Clement CM, McKnight RD, et al. The Canadian C-spine rule versus the NEXUS low-risk criteria in patients with trauma. N Engl J Med. 2003;349:2510–2518. 30 Wainner RS, Flynn TW, Whitman J. Spinal and Extremity Manipulation: The Basic Skill Set for Physical Therapists [CDROM]. San Antonio, TX: Manipulations Inc; 2001. 31 DeStefano LA, Greenman PE. Greenman’s Principles of Manual Medicine. 4th ed. Baltimore, MD: Lippincott Williams & Wilkins; 2011:537. 32 Costopoulos C, Patel RS, Mistry CD. Painful Horner’s syndrome. Emerg Med J. 2008;25:295. 33 West TE, Davies RJ, Kelly RE. Horner’s syndrome and headache due to carotid artery disease. Br Med J. 1976;1:818 – 820. 34 Baumgartner RW. Management of spontaneous dissection of the cervical carotid artery. Acta Neurochir Suppl. 2010;107: 57– 61. 35 Baumgartner RW, Bogousslavsky J. Clinical manifestations of carotid dissection. Front Neurol Neurosci. 2005;20:70 –76. 36 Chandra A, Suliman A, Angle N. Spontaneous dissection of the carotid and vertebral arteries: the 10-year UCSD experience. Ann Vasc Surg. 2007;21:178 –185. Volume 91 Number 8 Physical Therapy f 1273 Internal Carotid Artery Dissection 37 de Bray JM, Baumgartner RW. History of spontaneous dissection of the cervical carotid artery. Arch Neurol. 2005;62: 1168 –1170. 38 Leys D, Lucas C, Gobert M, et al. Cervical artery dissections. Eur Neurol. 1997; 37:3–12. 39 Smith L, Louw Q, Crous L, GrimmerSomers K. Prevalence of neck pain and headaches: impact of computer use and other associative factors. Cephalalgia. 2009;29:250 –257. 40 Parwar BL, Fawzi AA, Arnold AC, Schwartz SD. Horner’s syndrome and dissection of the internal carotid artery after chiropractic manipulation of the neck. Am J Ophthalmol. 2001;131:523–524. 1274 f Physical Therapy Volume 91 41 Debette S, Leys D. Cervical-artery dissections: predisposing factors, diagnosis, and outcome. Lancet Neurol. 2009;8:668 – 678. 42 Kerry R, Taylor AJ. Cervical arterial dysfunction: knowledge and reasoning for manual physical therapists. J Orthop Sports Phys Ther. 2009;39:378 –387. 43 Dallol B, Alsafadi H. Medical image: carotid dissection presenting as Horner’s syndrome. N Z Med J. 2010;123:88. 44 Schwartz NE, Vertinsky AT, Hirsch KG, Albers GW. Clinical and radiographic natural history of cervical artery dissections. J Stroke Cerebrovasc Dis. 2009;18:416–423. 45 Rigamonti A, Iurlaro S, Reganati P, et al. Cluster headache and internal carotid artery dissection: two cases and review of the literature. Headache. 2008;48:467– 470. Number 8 46 Rosebraugh CJ, Griebel DJ, DiPette DJ. A case report of carotid artery dissection presenting as cluster headache. Am J Med. 1997;102:418 – 419. 47 Frigerio S, Buhler R, Hess CW, Sturzenegger M. Symptomatic cluster headache in internal carotid artery dissection: consider anhidrosis. Headache. 2003;43:896 –900. 48 Mainardi F, Maggioni F, Dainese F, et al. Spontaneous carotid artery dissection with cluster-like headache. Cephalalgia. 2002;22:557–559. 49 Chan CC, Paine M, O’Day J. Carotid dissection: a common cause of Horner’s syndrome. Clin Experiment Ophthalmol. 2001;29:411– 415. August 2011 ProfessionWatch Vitalizing Practice Through Research and Research Through Practice: The Outcomes of a Conference to Enhance the Delivery of Care Marc S. Goldstein, David A. Scalzitti, Joanell A. Bohmert, Gerard P. Brennan, Rebecca L. Craik, Anthony Delitto, Edelle C. Field-Fote, Charles M. Magistro, Christopher M. Powers, Richard K. Shields T he American Physical Therapy Association (APTA) provided funding for a series of meetings among a small group of leaders representing the research and clinical communities whose task was to plan a conference, the outcome of which would be a “road map” for the process of generating evidence that would be implemented by clinicians so that the provision of services might be enhanced. Two of these planning sessions were held and resulted in a decision to focus a conference on the identification of strategies to lessen perceived “gaps” between physical therapist clinicians and researchers and the development of strategies to bridge the “gaps” between the 2 groups. These meetings ultimately resulted in the Vitalizing Practice Through Research and Research Through Practice Conference hosted by APTA. A perceived gap between research and practice has been cited as a problem by others within and outside the profession as well. In a recent editorial in the Journal of Orthopaedic and Sports Physical Therapy, Bechtel et al stated, “We have a problem in manual therapy, and perhaps in the whole profession of physical therapy. Our problem is the growing chasm between researchers on the one hand, and clinicians on the other.”1(p451) A recent Institute of Medicine workshop titled “Transforming Clinical Research in the United States: Challenges and Opportunities” echoed this theme and identified bridging August 2011 the divide between research and practice as one of the most critical needs facing clinical research.2 Discussion of the perceived gap between research and practice extends internationally, as Demers and Poissant3 lamented that research would be meaningless if it did not affect clinical practice. Furthermore, Demers and Poissant discussed the value of creating partnerships across the research process, from conception to dissemination of results. Translational Research Translational research, at its most macroscopic level, essentially refers to efficient movement of new discoveries into clinical practice. This research is typically connoted by the phrase “bench to bedside,” implying that the majority of translation is directional, from the basic science arena to the clinical arena. Authors define translational research slightly differently. Although a number of definitions for translational research exist,4 –7 we adopted for the conference the definition generated by the Institute for Translational Health Sciences (ITHS), a consortium of 38 medical research institutions supported by the National Institutes of Health, which defines translational research as moving knowledge and discovery gained from the basic sciences to its application in clinical and community settings.8 The ITHS model delineates 5 phases of translational research and labels the phases from T0 to T4 (Fig. 1). The model recognizes that translational research can be described via a continuum that extends from the identification of opportunities and approaches to a health problem (basic research), to the impact of practice on the health of the population (outcomes research).8 Furthermore, it should be recognized that the model is bidirectional and should not be interpreted as moving only from identification of opportunities and approaches to a health problem through the study of practice to population health impact. Regardless of the specific definition or model used to describe translational research, the goal is similar: to provide a framework that describes how basic and clinical research will interact in the future. Knowledge Translation Concomitant with an acknowledgment of the importance of the need for translational types of research is the recognition that an infrastructure needs to be developed so that the evidence created is utilized adequately. Thus, although the focus of translational research is the creation of new knowledge, there is a coexisting need to facilitate consistent application of the findings in practice. This concept of translating evidence into practice has been given a number of designations, among them “diffusion theory,”9 “implementation science,”10 and, more often, “knowledge translation.”11–17 Knowledge translation has been formally defined by the Canadian Institutes of Health Research as a dynamic and iterative process that includes the synthesis, dissemina- Volume 91 Number 8 Physical Therapy f 1275 ProfessionWatch: Outcomes of a Conference to Enhance the Delivery of Care T0 Identify problems, opportunities, and approaches T4 Evaluation of health impact on real-world populations Goal: Human Health Improvements T1 Discovery or foundational research T2 Health application to access efficacy T3 Health practice; science of dissemination and implementation Figure 1. The Institute for Translational Health Sciences (ITHS) model of translational research.8 tion, exchange, and ethically sound application of knowledge to improve health, provide more effective health services and products, and strengthen the health care system.13 Regardless of what it is called, the implementation of knowledge is as important as the creation of new knowledge and technologies to improve health outcomes.18 For a clinical science such as physical therapy, the importance of embracing the concept of knowledge translation should not be undervalued. Clearly, the issue of translating knowledge into practice is one that transcends physical therapy. It is a concern affecting all of health care. The lack of consistent implementation of evidence into practice is illustrated by McGlynn et 1276 f Physical Therapy Volume 91 al,19 who evaluated physician performance on 439 evidence-based indicators of quality of care for 30 common acute, chronic, or preventative conditions. Through telephone interviews and chart reviews across 12 US cities, the authors determined that patients received the right care at the right time less than 55% of the time. These results appear to represent a lack of timely translation of research findings into clinical practice and warrant our attention as physical therapists, as the authors stated that one solution to this issue is the routine availability of information on performance of providers. To provide an example related to physical therapy, a recent retrospective study demonstrated that adherence to recommendations of clinical practice guidelines in treatment of Number 8 people with acute low back pain was more likely to result in better clinical outcomes and lower costs.20 The rate of adherence to the guideline recommendations was 40.4%, which suggests that although clinical practice guidelines have been developed and following the recommendations may result in better care, active strategies are needed to increase awareness of the guidelines, implement the evidence in practice, and improve adherence. Given that both translational research and knowledge translation rely on a dynamic and iterative process, important infrastructure systems need to be in place throughout academia or other settings whose purpose is, in part, to create knowledge; throughout care delivery systems; and within funding sources. With this in mind, the Vitalizing Practice Through Research and Research Through Practice Conference was designed to reinforce to the profession the importance of translational research and to identify the need for infrastructure and resource development that would augment the existing research capability of physical therapists nationwide, as well as ensuring that this evidence is used to enhance practice. The success of the conference will be judged by how well it serves as the impetus for additional translational studies and leads to the creation of such an infrastructure, one that supports translational research and enhances knowledge translation. The Vitalizing Practice Through Research and Research Through Practice Conference With the goal of generating evidence and enhancing practice, as outlined above, as the incentive, the Vitalizing Practice Through Research and Research Through Practice Conference was planned over the course of August 2011 ProfessionWatch: Outcomes of a Conference to Enhance the Delivery of Care 2 meetings. The meetings were directed by a planning committee that had been appointed by the APTA Board of Directors and convened by APTA staff. Planning meeting discussions were guided by 2 assumptions: (1) the quality of physical therapy is threatened by the inappropriate variation in the care delivered, and (2) there is a lack of consistency or uniformity in tracking outcomes. The planning group acknowledged a need for the development of infrastructure to disseminate information to clinicians and to examine the effectiveness of evidence-based care delivery by measuring clinical and cost outcomes. In order to create processes for optimum care to be delivered to patients, the following were anticipated outcomes of the conference: • Clinician attendees would depart the conference with an understanding of what it means to have a systematic approach to data collection; • Development of a model for a minimum data set necessary to describe the process of care; • Creation of strategies to develop relationships with external stakeholders to enhance patient care delivery; and • Creation of new collaborations among researchers and clinicians to enhance patient care. Conference Design and Format The conference was designed to provide value to both researchers and clinicians. The themes discussed by the planning group attempted to ensure that conducted research would be useful to clinicians. Conversely, the relevant evidence generated from the research investigations would be adopted to enhance the delivery of care. Thus, the first phase of the conference recognized the importance of translational research August 2011 (ie, the movement of knowledge and discovery gained from research to its application in clinical and community settings).8 The second phase of the conference was designed to address infrastructure development. Topics such as development of databases, registries, and clinical research networks were deemed important, as the planning committee realized the creation of a hub from which studies could be conducted and results disseminated was vital to knowledge translation. To publicize the conference, a series of announcements using various media were used to disseminate the purpose of the conference and to invite nominations of the individual receiving the announcement or a colleague. Conference participants were selected by members of the planning committee using the following guidelines: (1) ensure adequate representation of clinicians and researchers, (2) select individuals who would act collegially, and (3) select participants who adhere to the principle that collaboration between clinicians and scientists will enhance clinical practice outcomes. Fifty-four participants were selected from 128 nominations (Appendix 1). Thirty-four of the participants considered themselves to be research investigators, and 20 considered themselves to be primarily clinicians. The participants ranged from individuals who were relatively new physical therapists to those with more than 40 years of experience. Nearly every setting in which physical therapists work was represented, although the largest number of participants were members of university faculties. A total of 75 individuals attended the conference, including the members of the planning committee and APTA staff members. The planning committee chose conference speakers who understood the concepts of translational research and knowledge translation as evidenced through publications and presentations. Each of the conference presentations had a common theme, which was the importance of translational research to the clinical community, payers, and policy makers. Speakers represented a mix of clinicians and researchers: 5 were physical therapist clinicians, and 4 were physical therapist researchers. Two speakers were from outside the physical therapy profession: one was a health services researcher, and one maintained both research and administrative responsibilities in a large health care system. The conference took place on December 2– 4, 2009, in Philadelphia, Pennsylvania. The majority of the presentations were recorded prior to the conference. Participants reviewed the presentations prior to attending the conference in preparation for active discussion (Appendix 2). Viewing these presentations ahead of time facilitated the accomplishment of the first anticipated outcome, which stated that participants would have an understanding of what it means to have a systematic approach to data collection. The core of the conference focused on guided discussions among participants. Four small groups, with an equal representation of clinicians and researchers, were charged to develop strategies to encourage researchers and clinicians to work more collaboratively. A member of the planning committee facilitated each group’s work. The groups’ discussion was guided by 2 basic questions—“Does research inform practice?” and Volume 91 Number 8 Physical Therapy f 1277 ProfessionWatch: Outcomes of a Conference to Enhance the Delivery of Care ● How well does research now inform practice? 䡩 Are there published results to support practice in key areas of practice? 䡩 Are these results widely disseminated? 䡩 Where there is good evidence, how well are the results implemented? 䡩 䡲 What are the barriers? 䡲 What are the solutions? What are the infrastructure needs to enhance researchers informing practice? ● How well does practice inform research? 䡩 Are practitioners provided an adequate venue to influence research questions? 䡩 Do researchers adequately value practitioner concerns (eg, reimbursement), enough to drive a research agenda or a specific study? 䡩 How do innovations in practice become elucidated? Is it necessary to take these findings to “the next level” (eg, corroborating research studies)? 䡩 What are the infrastructure needs to enhance practice informing researchers? Figure 2. Guiding questions for breakout sessions. “Does practice inform research?”— and a series of subquestions (Fig. 2). Answers to the questions were focused on how well research and practice currently inform each other and on identifying barriers to and solutions for optimal integration. Clinicians were encouraged to articulate how they can influence the behavior of researchers, and researchers were asked to describe ways their research could be made more useful to clinicians. This portion of the group discussion focused on issues such as: • Clinicians having the opportunity to influence the questions asked by researchers, • The value of clinician concerns when lines of research are formulated, • Clinical innovations serving as an impetus for additional study, and 1278 f Physical Therapy Volume 91 • The infrastructure necessary to create communication between clinicians and researchers. The questions do not necessarily relate to either the desired outcomes or foci of the conference. Rather, the planning group decided during the course of the meeting that the best way to generate discussion and guide the work of the breakout groups was to assign very generic questions and permit the discussions to lead in a direction that would result in appropriate responses to the original outcomes and foci. We are convinced that the strategy was a sound one, as the conference produced recommendations that exceeded the expectations of the planning group. These small-group deliberations were shared in a plenary session that Number 8 completed the activities of the second day. Summaries from each of the groups were very similar. The discussions generally could be categorized into the following themes: • Clinicians must determine methods to gain access to clinical information, including clinical guidelines. An underlying theme was the importance of clinical registries or databases. • There must be mutual respect and collaboration between the clinical and research communities. • Physical therapists should take advantage of research generated external to the profession as well as studies conducted by physical therapist scientists. • The appropriate outcomes measures should be specified and outcome instruments selected so that physical therapists can justify their interventions among both payers and policy makers. A health care economist discussed the need to develop an infrastructure to support the concept of valuebased practice. Value-based practice maintains that a patient’s values are pervasive and powerful parameters influencing decisions about health, clinical practice, and research.21 The session introduced the idea of valuebased practice, which is complementary to evidence-based practice, patient-centered care, and ethical care and provided the perspective on improving health care effectiveness by a stakeholder outside the profession. The conference concluded with participants identifying recommendations they felt were most essential. A number of themes emerged from this plenary session. The obvious central role of the patient in the process of care, as a driving motivation for research, was acknowledged and respected in this discussion. The August 2011 ProfessionWatch: Outcomes of a Conference to Enhance the Delivery of Care need for patients to assist in driving a research agenda is not novel.22,23 In response to recognition of the important role of the patient, the group discussed taking advantage of a variety of media platforms, similar to an iPhone application, to make decision support systems available to individual consumers potentially in need of physical therapy. Participants stressed that creating a collaborative culture would be costly and that all mechanisms of external funding should be explored to facilitate and bridge communication between the research and clinical communities, if the goals of translational research were to be accomplished. Recommendations and Conclusions Based on the deliberations of the small groups and the ensuing presentations during the plenary session, recommendations were made. These recommendations were consolidated by the planning committee into 4 key recommendations. These recommendations are not addressed to any one specific group; rather, the acknowledgment and implementation of the recommendations are the responsibility of the entire physical therapy profession. Recommendation 1 Identify mechanisms to distinguish conditions amenable to the development of clinical practice guidelines. The development of such guidelines will distinguish physical therapist practice that is supported by evidence from physical therapist practice that is not supported by evidence, as well as assist in the identification of outcomes. The recommendation of creation of guidelines is not a new or unique idea. As an example, APTA’s Section on Orthopaedics has already begun the process. The Canadian Medical Association, in its series on knowl- August 2011 edge translation, has strongly advocated for the use of guidelines.24 Furthermore, it has been cited that interventions to implement guidelines do, in fact, affect the process and outcomes of care, although the effect size (10%) is small.25 Simply creating guidelines and making them available to clinicians will not ensure that they will be widely used. Evidence of this statement abounds. In their widely cited article, McGlynn et al19 estimated that evidence-based health care is delivered to patients approximately 55% of the time. One strategy to assist in bridging the gap between evidence and practice is the expanded use of electronic databases to accelerate the diffusion of new evidence into practice. A goal of electronic databases is to make it easier for those who provide care by making evidence more readily available at the point of care.26 In a recent article, a group of researchers in the Netherlands demonstrated that adherence to evidence-based guidelines for low back pain resulted in greater improvement in patient functioning, lower utilization of care, and fewer treatment sessions.27 Although clinical guidelines are being developed and clinicians are using electronic databases,28 –32 recommendation 1 urges that these efforts be expanded. Recommendation 2 Develop clinical registries, minimum data sets, outcome databases, and core sets of outcome measures that cover the patient life span and the domains of ability and disability for each area of physical therapist practice. The coordination of local or, perhaps, national registries or databases is a necessity for developing the infrastructure to its optimum capacity. Patient registries are defined as an organized system that uses obser- vational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure and that serves one or more predetermined scientific, clinical, or policy purposes.33 Potential uses of a registry include the determination of clinical effectiveness and costeffectiveness of physical therapy intervention. Recommendation 3 Form a consultant group to investigate the development and implementation incentives for physical therapists to collect minimum data sets that are included within a clinical registry from which reports can be generated to develop optimal clinical practice guidelines, guide research, and enhance practice. The third recommendation is essentially an extension of the second recommendation and calls for the establishment of a consultant group, perhaps overseen by APTA, to administer development and implementation of these registries. This group will be integral to the success of all of the recommendations generated. Recommendation 4 Ensure that the consumer is the center of efforts for the provision of physical therapy services. There needs to be a transformation from the physical therapist as the “driver” of the provision of care; rather, it must be recognized that the consumer must be the beneficiary of services that are based on evidence. A primary theme of the conference was the recognition that researchers and clinicians must more effectively collaborate to benefit the physical therapy profession and our patients. These collaborations are to be devised so that the best care possi- Volume 91 Number 8 Physical Therapy f 1279 ProfessionWatch: Outcomes of a Conference to Enhance the Delivery of Care ble, at the least expense, can be provided to the patient. The patient should be at the core of any system that is developed and implemented. Throughout most of the history of health care, the clinician rather than the consumer has been the focus.26 The role of the patient cannot be overlooked in the development of new models that might be created as a result of the conference. A focus on the consumer is consistent with the outcomes of the recent APTA Physical Therapy and Society Summit (PASS)34 and with the focus of APTA’s Research Agenda.35 We realize that the recommendations specifically do not mirror the original anticipated outcomes of the conference. This slight lack of congruence was a result of the enthusiasm demonstrated by conference participants and their motivation to modify the outcomes initially developed by conference planners. We believe these new recommendations exceed, in value, the original anticipated outcomes of the conference. The Vitalizing Practice Through Research and Research Through Practice Conference provided a unique format for physical therapist researchers and clinicians to interact, plan, and prepare for the future of the profession. The dialogue provided a clear indication that: (1) the pursuit of translational research will have a definite impact on physical therapist practice, and (2) infrastructure will need to be developed so that physical therapy’s impact can be monitored not only at the level of an individual patient but also at the systems level. The dialogue also resulted in 4 recommendations to provide specific direction for meeting these goals. Based on anecdotal reports following the conference, the potential exists for substantive results to 1280 f Physical Therapy Volume 91 develop as a function of the efforts of those in attendance. The conference, however, was only the first step in “vitalizing practice and research.” An ongoing evaluation process will assess the implementation of the recommendations that were generated. The results of the evaluation process will truly measure the impact of the conference and determine its role in the creation of a larger cadre of clinical scientists who enhance the manner in which physical therapy care is currently delivered. The evaluation process will be based on the desire that conference recommendations must be implemented throughout the profession. These recommendations stress the idea that there needs to be more collaboration between clinicians and researchers than is currently the case. Conference participants cited examples where collaborative efforts have succeeded in improving patient care and reducing the costs of interventions, not only of physical therapy but of all therapeutic care provided throughout the episode. It is hoped that the examples cited at the conference will generalize across the profession and increase services that are based on evidence so that evidence- and value-based practice becomes the norm throughout the profession. The evaluation process cited above also will affect the entire profession. The first stage of the process involves presentations that have been made and will continue to be made at local, regional, and national meetings to describe the conference and inform audiences of the recommendations developed at the conference. However, this is only the initial step. Over time, those physical therapists who are practicing either based on evidence or in collaboration with researchers will be pro- Number 8 vided opportunities to share their experiences with groups of physical therapists as well. Dissemination of these experiences can lead to more collaboration, to the development of additional databases of evidence that can be contributed to and used by larger numbers of clinicians, and, ultimately, to the enhancement of patient care. One of the recommendations was that the client should be at the center of efforts for the provision of services and consumers must be the beneficiary of services based on evidence. The recognition of evidencebased services for the ultimate benefit of the client is motivating individual clinicians and networks. The conference can and will be judged successful if this mode of practice is adopted by a substantial proportion of the profession. Adoption of these recommendations will only enhance our status as a profession. Conference Evaluation Simply conducting a conference without assessing its value almost defeats the purpose of having a conference. Therefore, an extensive evaluation will be undertaken that will span into the future. The extended time frame is warranted, as it will likely take a substantial amount of time for the recommendations to be fully implemented. The evaluation of the effectiveness of the conference will follow a modified version of the CIPP (Context-InputProcess-Product) model developed by Stufflebeam.36,37 This model accounts for the context in which decisions have to be made. Thus, inputs, process, and outputs of a decision have to be evaluated. In the evaluation of this particular conference, we will have to account for behavioral changes of clinicians and researchers and cite how these changes affect the context or the environment in which services are August 2011 ProfessionWatch: Outcomes of a Conference to Enhance the Delivery of Care provided. Thus, the evaluation will proceed over a somewhat lengthy period of time until the profession can be confident that its services are provided in the optimum manner. M.S. Goldstein, EdD, American Physical Therapy Association, Alexandria, Virginia. Address all correspondence to Dr Goldstein at: [email protected]. The effectiveness evaluation model will be modified, as not all components are applicable. The portion of the model that deals with all postconference activities contains the most useful elements; these are the elements that will be used to assess the value of the conference. Thus, the evaluation will contain the following elements: J.A. Bohmert, PT, MS, Special Education, Anoka-Hennepin ISD 11, Anoka, Minnesota. • Impact evaluation, which assesses a program’s reach to the target audience, • Effectiveness evaluation, which assesses both the quality and significance of outcomes, and • Sustainability evaluation, which assesses the extent to which a program’s contributions are successfully institutionalized and continued over time.24 E.C. Field-Fote, PT, PhD, Department of Orthopaedics and Rehabilitation, University of Miami, Coral Gables, Florida. Given that the evaluation process will encompass a lengthy period of time, the expectation is that the conference is only the first step in a process that, ideally, will change the behaviors of both researchers and clinicians. Any discussion of a time frame would have to be couched in terms of increments. It is incumbent on conference planners to assess any adaptive behaviors over a period of years. [Goldstein MS, Scalzitti DA, Bohmert JA, et al. Vitalizing practice through research and research through practice: the outcomes of a conference to enhance the delivery of care. Phys Ther. 2011;91:1275–1284.] Having said that, however, during the upcoming year, a series of assessments will be made that will allow conference planners to determine at least the preliminary effects of the conference on the profession. At least 2 presentations involving a panel of conference participants will be given during the upcoming year. August 2011 D.A. Scalzitti, PT, PhD, OCS, American Physical Therapy Association. G.P. Brennan, PT, PhD, Physical Therapy Department, IHC Health Center–South Jordan, South Jordan, Utah. R.L. Craik, PT, PhD, FAPTA, Department of Physical Therapy, Arcadia University, Glenside, Pennsylvania. A. Delitto, PT, PhD, FAPTA, Department of Physical Therapy, University of Pittsburgh, Pittsburgh, Pennsylvania. C.M. Magistro, PT, FAPTA, Claremont, California. C.M. Powers, PT, PhD, Department of Biokinesiology & Physical Therapy, University of Southern California, Los Angeles, California. R.K. Shields, PT, PhD, FAPTA, Physical Therapy and Rehabilitation Sciences, Carver College of Medicine, University of Iowa, Iowa City, Iowa. All authors provided concept/idea/project design, writing, and consultation (including review of manuscript before submission). The authors would like to recognize and thank the following individuals for contributing to the conference and this article: Ralph Nitkin, PhD, and Daofen Chen, PT, PhD, who were instrumental in conference planning, and Steven Z. George, PT, PhD, and Gregory Hicks, PT, PhD, who reviewed and commented on an earlier draft of the manuscript. Their input is greatly appreciated. Published Ahead of Print: June 9, 2011 Accepted: April 15, 2011 Submitted: October 18, 2010 DOI: 10.2522/ptj.20100339 References 1 Bechtel R, Cleland J, Smith B. Researchers and clinicians: a growing divide or narrowing gap. J Orthop Sports Phys Ther. 2006; 36:451– 461. 2 English RA, Lebovitz Y, Giffin RB; Forum on Drug Discovery, Development, and Translation. Transforming Clinical Research in the United States: Challenges and Opportunities, Workshop Summary. Atlanta, GA: The National Academies Press; 2010. 3 Demers L, Poissant L. Connecting with clinicians: opportunities to strengthen rehabilitation research. Informa Healthcare. 2009;21:152–159. 4 Woolf SH. The meaning of translational research and why it matters. JAMA. 2008; 299:211–213. 5 Sung N, Crowley W Jr, Genel M, et al. Central challenges facing the national clinical research enterprise. JAMA. 2003;289: 1278 –1287. 6 Translational Research. The Ohio State University Medical Center. Available at: http://medicalcenter.osu.edu/research/ translational_research/Pages/index.aspx. Accessed April 20, 2010. 7 Salbach NM. Knowledge translation, evidence-based practice, and you. Physiother Can. 2010;62:293–294. 8 About Translational Research. Institute of Translational Health Sciences. Available at: http://www.iths.org/about/transla tional. Accessed July 9, 2010. 9 Green LW, Ottoson JM, Garcia C, Hiatt RA. Diffusion theory and knowledge dissemination, utilization, and integration in public health. Annu Rev Public Health. 2009; 30:151–174. 10 Madon T, Hofman KJ, Kupfer L, Glass RI. Implementation science. Science. 2007; 318:1728 –1729. 11 Choi BC. Understanding the basic principles of knowledge translation. J Epidemiol Community Health. 2005;59:93. 12 Rogers JD, Martin F. Knowledge translation in disability and rehabilitation research: lessons from the application of knowledge value mapping to the case of accessible currency. Journal of Disability Policy Studies. 2009;20:110 –126. 13 Straus SE, Tetroe J, Graham ID. Defining knowledge translation. CMAJ. 2009;181: 165–168. 14 Straus SE, Tetroe J, Graham ID. Knowledge Translation in Health Care: Moving from Evidence to Practice. Hoboken, NJ: Wiley-Blackwell; 2009. 15 Davis D, Davis N. Selecting educational interventions for knowledge translation. CMAJ. 2010;182:E89 –E93. 16 Brachaniec M, DePaul V, Elliott M, et al. Partnership in action: an innovative knowledge translation approach to improve outcomes for persons with fibromyalgia. Physiother Can. 2009;61:123– 127. Volume 91 Number 8 Physical Therapy f 1281 ProfessionWatch: Outcomes of a Conference to Enhance the Delivery of Care 17 Wensing M, Bosch M, Grol R. Developing and selecting interventions for translating knowledge to action. CMAJ. 2010;182: E85–E88. 18 Woolf SH, Johnson RE. The break-even point: when medical advances are less important than improving the fidelity with which they are delivered. Ann Fam Med. 2005;3:545–552. 19 McGlynn EA, Asch SM, Adams J, et al. The quality of health care delivered to adults in the United States. N Engl J Med. 2003;348: 2635–2645. 20 Fritz JM, Cleland JA, Brennan GP. Does adherence to the guideline recommendation for active treatments improve the quality of care for patients with acute low back pain delivered by physical therapists? Med Care. 2007;45:973–979. 21 Petrova M, Dale J, Fulford BK. Value-based practice in primary care: easing the tensions between individual values, ethical principles and best evidence. Br J Gen Pract. 2006;56:703–709. 22 Kjeken I, Ziegler C, Skrolsvik J, et al. How to develop patient-centered research: some perspectives based on surveys among people with rheumatic diseases in Scandinavia. Phys Ther. 2010;90:450 – 460. 23 Tallon D, Chard J, Dieppe P. Relation between agendas of the research community and the research consumer. Lancet. 2000;355:2037–2040. 24 Harrison M, Légaré F, Graham ID, Fervers B. Adapting clinical practice guidelines for local context and assessing barriers to their use. CMAJ. 2010;182:E78 –E84. 1282 f Physical Therapy Volume 91 25 Brouwers M, Stacey D, O’Connor A. Knowledge creation: synthesis, tools and products. CMAJ. 2010;182:E68 –E72. 26 Liang L. The gap between evidence and practice. Health Affairs. 2007;26:w119 – w121. 27 Rutten GM, Degen S, Hendriks EJ, et al. Adherence to clinical practice guidelines for low back pain in physical therapy: do patients benefit? Phys Ther. 2010;90: 1111–1122. 28 Etheredge LM. A rapid-learning health system. Health Affairs. 2007;26:w107–w118. 29 Granger CV, Markello SJ, Graham JE, et al. The Uniform Data System for Medical Rehabilitation: report of patients with traumatic brain injury discharged from rehabilitation programs in 2000 –2007. Am J Phys Med Rehabil. 2010;89: 265–278. 30 Duncan JR, Evens RG. Using information to optimize medical outcomes. JAMA. 2009;301:2383–2385. 31 Kerse N, Arroll B, Lloyd T, et al. Evidence databases, the Internet, and general practitioners: the New Zealand story. N Z Med J. 2001;114:89 –91. 32 Goldstein MS. Creating a culture of collaboration: vitalizing practice through research and research through practice. Presented at: Vitalizing Practice Through Research and Research Through Practice Conference; American Physical Therapy Association; December 2– 4, 2009; Philadelphia, Pennsylvania. Number 8 33 Gliklich RE, Dreyer NA, eds. Registries for Evaluating Patient Outcomes: A User’s Guide. 2nd ed. Rockville, MD: Agency for Healthcare Research and Quality; September 2010. AHRQ Publication No. 10EHC049. 34 Kigin CM, Rodgers MM, Wolf SL; PASS Steering Committee Members. The Physical Therapy and Society Summit (PASS) Meeting: observations and opportunities. Phys Ther. 2010;90:1555–1567. 35 Goldstein MS, Scalzitti DA, Craik RL, et al. The Revised Research Agenda for Physical Therapy. Phys Ther. 2011;91:165–174. 36 Guba EG, Lincoln YS. Effective Evaluation: Improving the Usefulness of Evaluation Results Through Responsive and Naturalistic Approaches. San Francisco, CA: Jossey-Bass Inc Publishers; 1981. 37 Stufflebeam DL. CIPP Evaluation Model Checklist: a tool for applying the fifth installment of the CIPP Model to assess long-term enterprises. Western Michigan University. June 2002. Available at: http://www. wmich.edu/evalctr/checklists/. Accessed September 2010. August 2011 ProfessionWatch: Outcomes of a Conference to Enhance the Delivery of Care Appendix 1. Conference Participants Stephanie Renee Albin, PT, OCS (Utah) Stephen C. Allison, PT, PhD (Arizona) Kristin Archer, PT, DPT, PhD (Tennessee) Skulpan Asavasopon, PT, MPT, OCS, FAAOMPT (California) Heather Lisa Atkinson, PT, DPT, NCS (New Jersey) George Beneck, PT, OCS (California) Stacey Lynn Brickson, PT, PhD, ATC (Wisconsin) David Alan Brown, PT, PhD (Illinois) Amy L. Castillo, PT, MPT, SCS, CSCS (Indiana) Prisca M. Collins, PT (Illinois) Chad Edward Cook, PT, PhD, MBA, FAAOMPT (Ohio) Judith Deutsch, PT, PhD (New Jersey) Reuben Escorpizo, PT (Florida) Linda V. Fetters, PT, PhD, FAPTA (California) Eileen Fowler, PT, PhD (California) Sara Francois, PT (Iowa) Julie M. Fritz, PT, PhD, ATC (Utah) Mary Lou Galantino, PT, PhD, MSCE (Delaware) Steven Z. George, PT, PhD (Florida) Laura Sisola Gilchrist, PT, PhD (Minnesota) Deborah Lynn Givens, PT, PhD, OCS (Ohio) Allan M. Glanzman, PT, DPT, PCS, ATP (Pennsylvania) Denise Gobert, PT, PhD (Texas) Joseph John Godges, PT, DPT, MA, OCS (California) Andrew Guccione, PT, DPT, PhD, FAPTA (Virginia) Robbin Ann Hickman, PT, DSc, PCS (Nevada) Gregory Evan Hicks, PT, PhD (Maryland) August 2011 Karen Holtgrefe, PT, DHS, OCS (Ohio) Thomas M. Howell, PT, MPT (Idaho) Eva Margareta Huey, PT (Ohio) Gail M. Jensen, PT, PhD, FAPTA (Nebraska) Diane U. Jette, PT, DSc (Vermont) Tara Jo Manal, PT, DPT, OCS, SCS (Delaware) Kathleen Kline Mangione, PT, PhD, GCS (Pennsylvania) Kimberly Susan Marryott-Lee, PT (Georgia) Michael Jeffrey Mueller, PT, PhD, FAPTA (Missouri) Kim A. Nixon-Cave, PT, PhD, PCS (New Jersey) Barbara J. Norton, PT, PhD, FAPTA (Missouri) Shreedevi Pandya, PT, MS (New York) Genevieve Pinto-Zipp, PT, EdD (New Jersey) Mary Jane K. Rapport, PT, DPT, PhD (Colorado) Clare E. Safran-Norton, PT, PhD, MS, OCS (Massachusetts) Karen Lohmann Siegel, PT (Maryland) Maureen Janet Simmonds, PT, PhD (Canada) Patricia L. Sinnott, PT, PhD, MPH (California) Beth Ann Smith, PT, DPT, PhD (Oregon) Cheryl Lynn Sparks, PT, DPT, OCS (Illinois) Scott Karl Stackhouse, PT, PhD (Pennsylvania) Katherine Sullivan, PT, PhD (California) Anne K. Swisher, PT, PhD, CCS (West Virginia) Anne Thackeray, PT (Utah) Leslie Torburn, PT, DPT (California) Robert S. Wainner, PT, PhD, ECS, OCS (Texas) Steven L. Wolf, PT, PhD, FAPTA (Georgia) Volume 91 Number 8 Physical Therapy f 1283 ProfessionWatch: Outcomes of a Conference to Enhance the Delivery of Care Appendix 2. Conference Presentationsa Prerecorded Audiovisual Presentations The Business Case of Quality Joseph Baumgaertner, PT, MS The Essential Components Larry Benz, PT, DPT, MBA, ECS Consumer-Driven Approach to Research Joanell A. Bohmert, PT, MS Improving Practice Through Clinical Research Gerard P. Brennan, PT, PhD Performance Assessment and Cost-Effectiveness Research Anthony Delitto, PT, PhD, FAPTA, and Pamela B. Peele, PhD A Systematic Approach to Physical Therapy Documentation Susan Horn, PhD Translating Clinical Research Into Improved Patient Outcomes Stephen Hunter, PT, OCS The Relevance of Translational Research in Physical Therapy Alan Jette, PT, PhD, FAPTA Engaging the Professional Workforce Mike Johnson, PT, PhD, OCS Private Practice, A Health System and Academia—It Can Work Paul Rockar, PT, DPT, MS Presentations On Site During the Conference Evolution of the Conference Marc S. Goldstein, EdD Vitalizing Practice Through Research and Research Through Practice: A Clinician’s Perspective Charles M. Magistro, PT, FAPTA Are You Ready? Rebecca L. Craik, PT, PhD, FAPTA Practice to Research to Practice: Cycle of Influence and Implementation Joseph J. Godges, PT, DPT, MA, OCS Elements for Change Pamela B. Peele, PhD a Information regarding the conference and the presentations is available at: http://www.apta.org/ResearchConference2009. 1284 f Physical Therapy Volume 91 Number 8 August 2011 Scholarships, Fellowships, and Grants News from the Foundation for Physical Therapy Recent Publications by Foundation-Funded Researchers “Appropriate Use of Diagnostic Imaging in Low Back Pain—A Reminder That Unnecessary Imaging May Do as Much Harm as Good,” by Flynn TW, Smith B, and Chou R, was published online in the Journal of Orthopaedic and Sports Physical Therapy on June 3, 2011. Timothy W. Flynn, PT, PhD, OCS, was awarded a 1996 Doctoral Training Research Grant and a 2000 Orthopaedic Section Research Grant. “Dual-Task Demands of Hand Movements for Adults With Stroke: A Pilot Study,” by Pohl PS, Kemper S, Siengsukon CF, Boyd L, Vidoni ED, and Herman RE, was published in Topics in Stroke Rehabilitation (2011;18[3]:238–247). Patricia S. Pohl, PT, PhD, was awarded Doctoral Training Research Grants in 1993 and 1994. “Low-Frequency H-Reflex Depression in Trained Human Soleus After Spinal Cord Injury,” by Shields RK, Dudley-Javoroski S, and Oza PD, was published in Neuroscience Letters (2011;499[2]:88– 92). Richard K. Shields, PT, PhD, FAPTA, was awarded Doctoral Training Research Grants in 1989 and 1990. “Lumbopelvic Landing Kinematics and EMG in Women With Contrasting Hip Strength,” by Popovich JM Jr, and Kulig K, was published online in Medicine and Science in Sports and Exercise on June 8, 2011. John M. Popovich Jr, PT, DPT, MS, was awarded Promotion of Doctoral Studies (PODS) I scholarships in 2005 and 2007 and a PODS II scholarship in 2008. August 2011 Foundation 8.11.indd 1285 “Predictors of Web-based Followup Response in the Prevention of Low Back Pain in the Military Trial (POLM),” by Childs JD, Teyhen DS, Van Wyngaarden JJ, Dougherty BF, Ladislas BJ, Helton GL, Robinson ME, Wu SS, and George SZ, was published online in BMC Musculoskeletal Disorders on June 13, 2011. John D. Childs, PT, PhD, MBA, OCS, CSCS, FAAOMPT, was awarded a PODS I scholarship in 2001 and the Pittsburgh– Marquette Research Grant in 2004. Steven Z. George, PT, PhD, MS, was awarded a PODS I scholarship in 2000 and a PODS II scholarship in 2001. “A Profile of Glenohumeral Internal and External Rotation Motion in the Uninjured High School Baseball Pitcher,” a 2-part article by Hurd WJ, Kaplan KM, Eiattrache NS, Jobe FW, Morrey BF, and Kaufman KR, was published in the Journal of Athletic Training (2011;46[3]:282–288 and 2011;46[3]:289–295). Wendy J. Hurd, PT, PhD, MS, was awarded the Mary McMillan Doctoral scholarship in 2002, a PODS I scholarship in 2003, and a PODS II scholarship in 2004. “Analysis of Shortened Versions of the Tampa Scale for Kinesiophobia and Pain Catastrophizing Scale for Patients After Anterior Cruciate Ligament Reconstruction,” by George SZ, Lentz TA, Zeppieri G, Lee D, and Chmielewski TL, was published online in The Clinical Journal of Pain on June 14, 2011. Steven Z. George, PT, PhD, MS, was awarded a PODS I scholarship in 2000 and a PODS II scholarship in 2001. “Age-Related Differences in Muscle Fatigue Vary by Contraction Type: A Meta-analysis,” by Keith G. Avin, PT, MPT, MS, and Laura A. Frey Law, PT, PhD, MS, was published in Physical Therapy (2011;91[8]:1153–1165]. Avin was awarded a Florence P. Kendall scholarship in 2008, a PODS I scholarship in 2009, and a PODS II scholarship in 2010. Frey Law was awarded a McMillan Doctoral scholarship in 2000, a PODS I scholarship in 2001, and a PODS II scholarship in 2002. Foundation Announces Winning Schools of Pittsburgh–Marquette Challenge The Foundation announced the winners of the Pittsburgh– Marquette Challenge at its annual gala on June 9 at National Harbor, Maryland. Physical therapist and physical therapist assistant students from 62 schools across the country raised a record-breaking $264,274 to support physical therapy research. In 23 years, the Challenge has raised more than $2 million to benefit the Foundation. Congratulations to the winning schools of the Pittsburgh– Marquette Challenge: • • • 1st Place: University of Pittsburgh ($56,800); 2nd Place: Sacred Heart University ($31,600); 3rd Place: Emory University ($23,800). Volume 91 Number 8 Physical Therapy ■ 1285 7/8/11 1:22 PM Scholarships, Fellowships, and Grants Award of Merit (donating $6,000 or more): Rosalind Franklin University, Somerset Community College, University of Delaware, University of Miami, University of North Carolina–Chapel Hill, and Virginia Commonwealth University. Honorable Mention (donating $3,000 or more): Arcadia University, Boston University, Lynchburg College, Mayo School of Health Science, MGH Institute of Health Professions, Midwestern University, Northeastern University, Northwestern University, Simmons College, University of Alabama at Birmingham, University of Evansville, University of Iowa, University of Oklahoma, University of St Augustine, and Washington University in St Louis. Kendall scholarship. Foundation Research Grants are available for either 1- or 2-year projects for new and emerging investigators. Applications are due August 17, 2011, at 12:00 pm, noon, ET. For more details or to apply, please visit Foundation4PT.org/apply-forfunding. Share Your Research News and Announcements With the Foundation To have your information posted in the Foundation’s section of Physical Therapy, please e-mail our Program Assistant, Rachael Crockett, at RachaelCrockett@Foundation4PT. org. Stay Connected With the Foundation in 3 Easy Ways 1. www.facebook.com/foundation 4PT. 2. Check out our Web Foundation4PT.org. site: 3. Subscribe to our monthly newsletter for updates on our donors, researchers, events, and much more! E-mail AbegailMatienzo@ Foundation4PT.org to sign up today. [DOI: 10.2522/ptj.2011.91.8.1285] Special Awards: • • • Most Successful Newcomer: Lynchburg College; Biggest Stretch School: University of North Carolina– Chapel Hill; Most Successful PTA School: Somerset Community College. For a complete listing of schools that participated in the Pittsburgh–Marquette Challenge, visit the Foundation’s Web site. The 2011–2012 Pittsburgh–Marquette Challenge kicks off at the National Student Conclave in Minneapolis, Minnesota, on October 21, 2011. Current Funding Opportunities The Foundation is now accepting applications for the Florence P. Kendall Doctoral scholarship, Foundation Research Grant, and Magistro Family Foundation Research Grant. Students beginning their postprofessional doctoral programs are encouraged to apply for a $5,000 Any Amount—Every Month—Leads to ExcePTional Results Your Participation Matters Every Gift Counts The Foundation for Physical Therapy’s excePTional giving program allows the Foundation to direct funds to areas with the most urgent needs, and it all starts with you. Monthly or quarterly gifts provide sustained revenue that let the Foundation plan for the future. The benefits are endless. The Foundation for Physical Therapy equips new researchers to make a difference in our world. Your support of the excePTional monthly giving program makes this possible by providing the resources necessary to fund postprofessional doctoral scholarships, fellowships, and research grants. Your investment in your colleagues’ talents and energy, and in all they will accomplish for the world that awaits them, will have an impact on our profession and health care for decades to come. Your gift is automatically charged to your credit card each month or quarter. You retain full control and can modify or cancel future gifts at any time. At the end of the year, you will receive an itemized receipt for your gifts. Gifts of $10 per month become $120 a year; gifts of $84 per month become more than $1,000 a year! 1286 ■ Physical Therapy Volume 91 Number 8 Foundation 8.11.indd 1286 To make a gift today, please visit Foundation4PT.org/Get-Involved/ Donate. To learn more about joining the excePTional program, visit Foundation4pt.kintera.org/become exceptional. For more information, contact Rachael Estep, assistant director of development, 800/875-1378, RachaelEstep @Foundation4PT.org. August 2011 7/18/11 10:51 AM Product Highlights two procedures, two great products zero waste. www.parkerlabs.com/polysonic.html (Continued) Index to General Information Found at: www.apta.org Physical Therapy (PTJ) Accredited Education Programs ............http://www.capteonline.org/Programs/ Awards ..................... http://www.apta.org/HonorsAwards/ Bylaws ................................. http://www.apta.org/Policies/ Call for Nominations .......... http://www.apta.org/Elections/ Code of Ethics .................................... http://www.apta.org/ CoreDocuments/ Abstracts of Papers Accepted for Presentation at Annual Conference (added every May) ............................ ptjournal.apta.org/ site/misc/annualcon.xhtml Submission Guidelines .......................... ptjournal.apta.org/ site/misc/ifora.xhtml In Memoriam............................................................March Index (Author/Subject) .......................................December Mary McMillan Lecture ...................................... November Membership Statistics ..................................................June Presidential Address ........................................... November Statement of Ownership .....................................December August 2011 Volume 91 Number 8 Physical Therapy ■ 1287 Product Highlights Make patients . Greet our all new product line at totalgym.com/new Call now 800-541-4900. Learn more @ © 2011 EFI Corp. dba Total Gym Ad Index Allergan ........................................................ Cover 3 Gebauer ........................................................... 1145 Home Depot..................................................... 1145 Parker Laboratories ....................................... Cover 4 Preferred Therapy Providers .......................... Cover 2 Request FREE Product Information on products advertised in PTJ. Go to APTA’s online resource at: http://www.apta.org/freeproductinfo 1288 ■ Physical Therapy Volume 91 Number 8 August 2011