Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
NCT06088355

Moderate Versus High Volume Light-Moderate Intensity Exercise for People With Moderate Parkinson's Disease

Led by VA Office of Research and Development · Updated on 2026-02-05

123

Participants Needed

1

Research Sites

227 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Veterans with mid to later stage Parkinson's disease (PD) may not be able to work out as hard as they need to, to prevent brain cell loss. Maybe they could work out longer and more frequently to make up for this during their good times and good weeks and then rest during the bad weeks. The investigators will compare how effective working out a lot one week per month with a break of three weeks is to continuously exercising weekly with no breaks in people with mid stage PD. The investigators will look at how fast participants walk per minute, whether they become more physically active, the biochemicals in their blood, and at how stiff their blood vessels are before and after the exercise.

CONDITIONS

Official Title

Moderate Versus High Volume Light-Moderate Intensity Exercise for People With Moderate Parkinson's Disease

Who Can Participate

Age: 40Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 40 years or older
  • Diagnosis of definite Parkinson's disease by a board-certified Movement Disorders Neurologist
  • Hoehn and Yahr stages 2, 2.5, or 3 of Parkinson's disease
  • Montreal Cognitive Assessment (MoCA) score greater than 17
  • Able to walk at least 10 feet with or without an assistive device
  • Best corrected/aided vision better than 20/70 in the better eye
  • Show clear symptom improvement from antiparkinsonian medications such as levodopa
  • Fluent in English and able to comprehend and participate
  • Willing to be randomized to a treatment group
Not Eligible

You will not qualify if you...

  • Untreated major depression or major psychiatric illness
  • History of stroke or traumatic brain injury
  • Hearing loss with average sensitivity worse than 40 dB at 0.5, 1.0, and 2.0 kHz
  • History of alcohol abuse or use of antipsychotic medications
  • Planning to be away from the area for more than 1 month during the study
  • Taking moderate to high doses of beta-blockers with resting heart rate below 60 beats per minute
  • Severe cardiac disease such as advanced congestive heart failure, significant aortic stenosis, history of cardiac arrest, use of cardiac defibrillator, or uncontrolled angina
  • Other significant health conditions that impair exercise participation, including renal failure on hemodialysis or excessive alcohol use exceeding 14 drinks per week

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Atlanta VA Medical and Rehab Center, Decatur, GA

Decatur, Georgia, United States, 30033-4004

Actively Recruiting

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Research Team

M

Madeleine E Hackney, PhD

CONTACT

J

Joe R Nocera, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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