Barre Exercise in Parkinson's
- Conditions
- Parkinson Disease
- Registration Number
- NCT06203990
- Lead Sponsor
- Washington University School of Medicine
- Brief Summary
This study asks if a barre exercise program is a feasible and acceptable form of exercise for individuals with Parkinson disease. The study will also evaluate barre's potential effects on motor outcomes, including balance, strength, and functional mobility.
- Detailed Description
The primary objectives of this study are to: 1) evaluate the feasibility and acceptability of a barre exercise intervention and 2) gather preliminary data regarding the effect of a barre exercise intervention on balance, strength, functional mobility and quality of life in individuals with mild to moderate Parkinson disease (PD). Individuals with PD (N=15) will be recruited to participate in a pilot barre exercise class led by a certified barre instructor. The intervention will include 24, 45-50 minute group classes (twice weekly for 12 weeks, excluding holidays). Pre- and post-intervention data collection will include assessments of balance, lower extremity strength, and functional mobility.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 13
- diagnosed by a neurologist with idiopathic Parkinson disease
- at least 18 years of age
- a score on the Hoehn & Yahr (H&Y) scale between I-III to indicate mild to moderate disease severity
- able to provide informed consent
- able to walk for 10 continuous minutes without assistance from another person
- stable medication regimen for at least one month prior to enrollment
- any neurological condition other than PD
- history of orthopedic or other medical conditions that limit the ability to safely participate in the intervention or
- language, visual, or hearing barriers to participation
- evidence of dementia (Montreal Cognitive Assessment < 24) to ensure understanding of the intervention class instructions
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Attendance 12 weeks Number of participants who attended at least 75% of the classes
Retention (Study Completion) 12 weeks Percent of participants who remained enrolled for the duration of the study
Acceptability 12 weeks Mean group rating on the Client Satisfaction Questionnaire, a standardized measure using Likert-scale questions to assess self-reported satisfaction of a program. Range is 1-4, higher scores indicate higher satisfaction
- Secondary Outcome Measures
Name Time Method Functional Strength 12 weeks Mean change in time taken to complete five sit to stand movements pre- to post- intervention, measured in seconds. Longer time indicates worse performance.
Gait 12 weeks Mean change in gait speed pre- to post-intervention, measured in meters/second.
Balance 12 weeks Mean change in total score on the Mini Balance Evaluation Systems Test (Mini-BESTest) from pre- to post-intervention. The Mini-BESTest is a brief, clinically relevant assessment of balance, scored on a scale from 0 to 28, with higher scores indicating better balance. A negative change score reflects a decline in balance performance from pre- to post-intervention.
Trial Locations
- Locations (1)
Washington University School of Medicine
🇺🇸Saint Louis, Missouri, United States
Washington University School of Medicine🇺🇸Saint Louis, Missouri, United States