RecruitingNot ApplicableNCT06707402

The Effects of 24-Weeks Community-based Brisk Walking in People With Parkinson's Disease

The Effects of 24 Weeks Community-based Brisk Walking on Physical Function, Comorbidities, Cognition, Disease Severity, and Health-related Quality of Life in People With Parkinson's Disease.


Sponsor

University of Aarhus

Enrollment

129 participants

Start Date

Mar 11, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to investigate if brisk walking can improve walking function in people with Parkinson's disease and what kind of brisk walking intervention that is most effective. The main questions are: If brisk walking can reduce self-perceived walking difficulty What type of exercise intervention is most effective. Researchers will compare a brisk walking group receiving a personalized walking program with a group receiving an activity tracker and a control group. Participants will * be tested at baseline (0 weeks), post the intervention period (24 weeks) and after a follow-up period (48 weeks). * be randomly allocated to one of three groups at baseline. * follow the prescribed intervention they are allocated to.


Eligibility

Min Age: 40 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a structured 24-week community-based brisk walking program can improve walking ability, balance, and quality of life in people with Parkinson's disease. **You may be eligible if...** - You have been clinically diagnosed with Parkinson's disease - You are 40 years old or older - Your Parkinson's is in an early-to-moderate stage (Hoehn and Yahr stage 3 or less) - You have noticeable walking difficulties - You can travel independently to training sessions and test days - You expect to be able to attend at least 85% of sessions **You may NOT be eligible if...** - You have another neurological disorder or severe arthritis that affects your walking - You are pregnant - You have significant dementia - You have alcohol dependency or serious heart, lung, or metabolic conditions that make exercise unsafe Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALWALK

The intervention covers a personalized 24-week progressive brisk walking program. The program consists of moderate to high-intensity walking (i.e., 55-85% maximal heart rate) performed as both continuous and interval training sessions 2-3 times/week lasting 30-60 min/session. Four individually supervised sessions will be conducted in the first 2 weeks, while 1 supervised group session will be received bi-weekly. Furthermore, the group will receive an activity tracker and monthly telephone calls will be offered to adjust the intensity of the program (if necessary), clarify any questions regarding the intervention, and give verbal motivation. At the baseline assessment and at week 12, during a group training session, the figure of 8 walk test will be conducted to gain insigh tinto the current status of the training program. Lastly, after completion of the baseline test, the participants are given a brief educational session (walking advice) on recommended guidelines for physical activity

BEHAVIORALACTIVE

Will receive an activity tracker is provided alongside monthly telephone calls and walking advice after the baseline test. Similar to WALK, 3 telephone calls are provided during the follow-up period.

BEHAVIORALCON

Receives a brief educational session (walking advice) is provided at baseline, after which no further contacts are made.


Locations(1)

Aarhus University, Department of Public Health, Sport Science

Aarhus C, Denmark

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NCT06707402


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