Walking may slow Parkinson's: new study tests aerobic exercise
NCT ID NCT03808675
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tested whether long-term aerobic walking can slow the progression of Parkinson's disease. 57 people with mild-to-moderate Parkinson's walked for 150 minutes per week at a moderate pace. Researchers measured changes in movement, thinking, driving safety, and brain health. If effective, aerobic exercise could become an immediate, low-cost treatment option.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- aerobic walking exercise
- What this could lead to
- If it works, this could provide a low-cost, accessible way to slow Parkinson's progression and improve movement, thinking, and driving safety.
- What could go wrong
- This is a small, early-stage study with only 57 participants. Exercise may not slow the disease for everyone, and benefits might be modest or temporary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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57 people
The number who actually took part.
- Started
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Jul 2019
- Finished
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Sep 2024
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Men or women aged 40 and older with the diagnosis of idiopathic PD per UK Brain Bank criteria * Hoehn-Yahr Stage I-III, on stable dopaminergic treatment regimen for equal or greater than 4 weeks prior to baseline. * Aerobic Fitness: VO2max below "very good" fitness levels for their age and gender at baseline cyle ergometry. To include subjects who have room to improve their aerobic fitness, the investigators will enroll only those subjects whose VO2max is below "very good" fitness level (about 90% of the population) using age and gender based VO2max norms based review of 62 studies where VO2max was measured directly in healthy adult subjects in the USA, Canada and 7 European countries (Reference: Shvartz, E and Reibold, RC. Aerobic fitness norms for males and females aged 6 to 75 years: a review. Aviat Space Environ Med. 1990; 61:3-11). * Cognitive function: No dementia per Movement Disorder Society Level I criteria (Reference: Dubois, B, Burn, D, Goetz, C, et al. Diagnostic procedures for Parkinson's disease dementia: recommendations from the movement disorder society task force. Mov Disord. 2007; 22:2314-2324). * Current active drivers with a valid driver's license * Veteran or non-veteran Exclusion Criteria: * Subjects unwilling or unable to give informed consent * Secondary parkinsonism (e.g., drug induced) * Parkinson-plus syndromes * History of brain surgery for PD such as deep brain stimulation * Corrected visual acuity less than 20/50 (due to effect on driving) * Contraindications to exercise per ACSM criteria for Exercise Testing and Training (Reference: American College of Sports Medicine. Cardiorespiratory Exercise Prescription. In: Ehrman JK, ed. ACSM's Guidelines for Exercise Testing and Prescription.6th ed. Baltimore: Lippincott Williams \& Wilkins, 2010:448-462). * No confounding acute or unstable medical, psychiatric, orthopedic condition. Subjects who have hypertension, diabetes mellitus, depression, or other common age related illness will be included if their disease under control with stable treatment regimen for at least 30 days. * Clinically significant TBI or PTSD * Presence of other known medical or psychiatric comorbidity that in the investigator's opinion would compromise participation in the study * Presence of dementia per Movement Disorder Society Level I criteria * Subjects with clinically significant depression as determined by a Beck Depression Inventory (BDI) score greater than 15 at the screening visit * History of exposure to typical or atypical antipsychotics or other dopamine blocking agents within 6 months prior to the baseline visit * Use of investigational drugs within 30 days before screening * Subjects have to be on a stable regimen of central nervous system acting medications (benzodiazepines, antidepressants, hypnotics) for 30 days prior to the baseline visit * Contraindication to having a brain MRI
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Iowa City VA Health Care System, Iowa City, IA
Iowa City, Iowa, 52246-2292, United States
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University of Iowa Hospitals & Clinics
Iowa City, Iowa, 52242, United States
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Other studies related to the condition(s) this trial covers.
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