Actively Recruiting
The Active Transition Home Post-Stroke Program
Led by University of British Columbia · Updated on 2025-07-18
20
Participants Needed
1
Research Sites
95 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Post-stroke participants will wear wearable sensors for one week at 1-week prior to discharge from inpatient rehabilitation, 3- and 7- weeks post-discharge and 3-months post-discharge. All participants will wear sensors but only participants in the intervention group will receive sensor-informed activity feedback (e.g., activity, sleep and sedentary behaviour) and feedback informed goal setting sessions with a physiotherapist. The feedback forms will be co-created with physiotherapists working at GF Strong. Focus group(s) will be conducted to collect the opinions of clinicians with respect to measures to be included in the feedback form. At 3-months post-discharge, participants will be interviewed regarding their experience with the sensors. This study will explore the feasibility and initial benefits of using wearable sensors paired with goal setting to assist in the maintenance of activity levels during a difficult period for stroke survivors (transitioning home from rehab).
CONDITIONS
Official Title
The Active Transition Home Post-Stroke Program
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age of 18 or older
- Had a stroke resulting in hemiparesis
- English speaking or living with an English-speaking family member to assist with interpretation and goal setting with a physiotherapist
You will not qualify if you...
- Presents with any unstable medical conditions that would impact activity (e.g., unstable cardiac condition, recent fracture)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
GF Strong Rehabilitation Centre
Vancouver, British Columbia, Canada, V5Z 2G9
Actively Recruiting
Research Team
C
Courtney Pollock, PhD
CONTACT
A
Aishwarya Shenoy
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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