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Completed

NCT Number: NCT06203990

Barre Exercise in Parkinson's

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Washington University School of Medicine

St Louis, Missouri, 63108, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Barre exercise

Behavioral

Group barre exercise class

Primary outcomes

  1. Attendance

    Time frame: 12 weeks

    Number of participants who attended at least 75% of the classes

  2. Retention (Study Completion)

    Time frame: 12 weeks

    Percent of participants who remained enrolled for the duration of the study

  3. Acceptability

    Time frame: 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 outcomes

  1. Balance

    Time frame: 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.

  2. Functional Strength

    Time frame: 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.

  3. Gait

    Time frame: 12 weeks

    Mean change in gait speed pre- to post-intervention, measured in meters/second.

Sponsors and collaborators

Lead sponsor

Washington University School of Medicine

Other

Registry information

Official study title

Barre Exercise for People With Parkinson Disease

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jan 12, 2024
Registry last updated
Jun 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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