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Clinical Trials in Canada / NCT06915987
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Parkinson Disease and Exercise Snacks

NCT06915987 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-05-15
Last updated
2025-04-15

Condition(s) studied

Parkinson Disease

Investigational drug(s) / intervention(s)

Exercise Intervention

Exercise Intervention: Exercise snack group will be higher intensity movements designed to elevate heart rate while active movement break will have low intensity / stretching exercises assigned to them.

Study summary

People with Parkinson's Disease (PD) benefit from exercise, but many face barriers like motor disability, fatigue, and lack of time, leading to reduced activity. This study aims to assess the effectiveness of "exercise snacks," short bursts of vigorous activity that can be done anywhere without equipment or a significant time commitment. These exercise snacks help integrate activity into daily life, making it more accessible for people with PD. The secondary goal is to evaluate the feasibility of this approach through this pilot randomized controlled trial (RCT) to inform a larger, future RCT.

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (19 years of age or older) with Clinically Established PD (Postuma et al., 2015). * Medically cleared to exercise by their physician. * A score of ≤3 on the modified Hoehn \& Yahr scale (i.e. physically independent, may have unilateral or bilateral clinical signs, including mild impairment of postural reflexes). * Have access to a computer, tablet, or smartphone with internet connection for intervention delivery and tracking. Exclusion criteria * Comorbid condition with physical disability preventing participation in exercise (i.e., that cannot be accommodated with modifications to the prescribed exercise). * A score of \>=4 on the modified Hoehn \& Yahr scale (meaning they may be able to stand or walk but are not physically independent; this typically includes a need for gait aids such as a cane or walker) * No access to reliable internet connection. * Are currently participating in another clinical trial that would interfere with the study procedures described. * Have a scheduled event (e.g. medical or surgical procedure, prolonged travel in the next 3-4 months) that would interrupt participation in the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of British Columbia Okanagan Kelowna British Columbia

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06915987 on ClinicalTrials.gov ↗ ← All trials in Canada