Wearable sensors may help stroke survivors stay active after rehab
NCT ID NCT06119230
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This study tests whether wearable sensors and goal-setting sessions with a physiotherapist can help stroke survivors stay active after leaving inpatient rehabilitation. Participants wear sensors to track activity, sleep, and sedentary behavior, and some receive feedback and set goals based on that data. The study includes 20 stroke survivors and also gathers input from physiotherapists. Researchers will measure feasibility, adherence, and changes in mobility and function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Wearable sensors paired with activity counselling and goal-setting sessions with a physiotherapist
- What this could lead to
- If this approach works, it could help stroke survivors maintain their activity levels and independence after leaving rehabilitation.
- What could go wrong
- This is a small feasibility study with only 20 participants, so results may not apply widely. The intervention may not be practical or effective for everyone.
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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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20 people
The number who actually took part.
- Started
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Feb 2024
- Finished
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Apr 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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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18 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: Physiotherapists for focus group participation * Age of 18 or older * Registered Physiotherapist at GF Strong (inpatient or outpatient) * 1 year of work experience in stroke rehabilitation (acute or chronic) Patient Group * 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/goal setting with PT Exclusion Criteria: Physiotherapist Focus Group: \- \<1 year of experience in stroke rehabilitation Patient Group: \- presents with any other unstable medical conditions that would impact activity (e.g., unstable cardiac condition, recent fracture)
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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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GF Strong Rehabilitation Centre
Vancouver, British Columbia, V5Z 2G9, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Correlation of visual and motor deficits in stroke patients
- Pilot study on the effects induced by an electromyographic-controlled functional electrical stimulator (FitFES) for upper limb rehabilitation in post-stroke patients
- Brazilian version of a behavior change intervention to support healthy lifestyle adoption after stroke - iVIDAVC: protocol for a pilot randomized study
- Determination of efficacy of sustained motor contraction generated using StimWave peripheral nerve stimulator
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