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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06203990
Other study ID # 202312097
Secondary ID
Status Active, not recruiting
Phase Phase 1
First received
Last updated
Start date January 2, 2024
Est. completion date May 20, 2024

Study information

Verified date March 2024
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Active, not recruiting
Enrollment 15
Est. completion date May 20, 2024
Est. primary completion date May 20, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 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 Exclusion Criteria: - 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


Related Conditions & MeSH terms


Intervention

Behavioral:
Barre exercise
Group barre exercise class

Locations

Country Name City State
United States Washington University School of Medicine Saint Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Attendance Percent of clases attended 12 weeks
Primary Study Completion Percent of participants who finish full study 12 weeks
Secondary Balance Change in score on Mini-BESTest 12 weeks
Secondary Functional Strength Change in time to complete five sit to stand movements 12 weeks
Secondary Gait Change in gait speed 12 weeks
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