Interactive game tracks stroke recovery to personalize rehab
NCT ID NCT06806761
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This study follows 100 stroke survivors over six months to understand how sitting balance, standing balance, and walking recover. Using wearable sensors and an interactive assessment game, researchers measure movement, coordination, and reaction time. The goal is to identify recovery patterns that can guide tailored rehabilitation strategies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to personalized rehabilitation plans that improve recovery of balance and walking after stroke.
- What could go wrong
- This is an observational study, not a treatment trial. It may not identify clear recovery patterns, and results may not apply to all stroke survivors.
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.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2025
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- 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.
Who is studied
Patients in the first 6 months after stroke: Participants will be adults aged 18 years or older who have experienced a supratentorial ischaemic or haemorrhagic stroke and are included within eight weeks after stroke onset. They will be followed during the first six months after stroke.
- Ages
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18 years and older
- Sex
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Anyone
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: * Adult aged ≥18 years * Diagnosis of a supratentorial ischaemic or haemorrhagic stroke * Within the first eight weeks after stroke onset at the time of inclusion * Able to understand and perform the study procedures that are feasible at a given assessment time point, based on the advice of the treating therapist(s) and/or physician(s) * Written informed consent provided by the participant or, where applicable, by a legally authorised representative Exclusion Criteria: * Neurological or orthopaedic comorbidities unrelated to stroke that significantly impair motor function * Severe medical conditions that could compromise safety during the assessments * Major deficits in communication, memory or understanding that prevent participation in the study procedures * Insufficient comprehension of Dutch, French, German or English
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Inkendaal rehabilitation hospital
RECRUITINGSint-Pieters-Leeuw, Brussels Capital, 1602, Belgium
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