Can a robot unlock the Brain's recovery after stroke?
NCT ID NCT04171856
First seen Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time
Summary
This study investigates whether people who recently had a stroke (within 21 days) can learn new arm movements using a rehabilitation robot called REAplan. Researchers will compare their learning ability with healthy individuals and those who had a stroke long ago. The goal is to understand how different brain regions affected by stroke influence motor skill learning, which could inform future rehabilitation approaches.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- REAplan(R) rehabilitation robot for motor skill learning with the affected arm
- What this could lead to
- If successful, this could reveal how the brain learns motor skills after stroke, potentially guiding more effective rehabilitation strategies.
- What could go wrong
- This is an exploratory study, not a treatment trial. Results may not translate into direct clinical benefits, and individual outcomes could vary widely.
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.
- 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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About 245 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2020
- Expected to finish
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Jul 2040
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.
- Ages
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18 to 90 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
ACUTE STROKE PATIENTS: Inclusion Criteria: * acute stroke (\> 21 days) * aged 18-90 years * with a stroke lesion on brain imaging Exclusion Criteria: * " classical " contre-indication to MRI (non-MR-compatible pacemaker, pregnancy, non-MR-compatible implanted devices, claustrophoby, etc ...) * difficulty in understanding or executing commands * drug/alcohol abuse * severe aphasia / cognitive deficits interfering with study * inability to voluntarily move the affected arm (i.e. complete paralysis of the arm) * multiple strokes / dementia / psychiatric condition PATIENTS WITH TRANSIENT GLOBAL AMNESIA: Clinical diagnosis, criteria of Hodge \& Warlow (1990): * Anterograde amnesia observed by a witness * No alteration of consciousness or loss of identity * Cognitive dysfunction limited to amnesia * Lack of focused neurological deficit or argument for a comitiality * Absence of head trauma * Symptom resolution within 24 hours * Possible existence of vegetative symptoms Inclusion criteria: * Transient global amnesia * 8-90 years old * Be able to perform 3 consecutive sessions on a rehabilitation robot Exclusion criteria: * Severe aphasia / cognitive deficits interfering with study * Psychiatric disorders * Alcohol / drug addiction * Exclusion criteria related to MRI HEALTHY INDIVIDUALS: Inclusion Criteria: • 18-90 years Exclusion Criteria: * medical history with a previous stroke/neurological deficit * drug/alcohol abuse * psychiatric condition/ dementia CHRONIC STROKE PATIENTS: Inclusion Criteria: * chronic stroke (\>6 months) * aged 18-90 years * with a stroke lesion on brain imaging Exclusion Criteria: * difficulty in understanding or executing commands * drug/alcohol abuse * severe aphasia / cognitive deficits interfering with study * inability to voluntarily move the affected arm (i.e. complete paralysis of the arm) * multiple strokes / dementia / psychiatric condition
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Genom att skicka in godkänner du våra Användarvillkor
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
2 sites. 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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CHU UCL Namur
RECRUITINGYvoir, Namur, 5530, Belgium
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University Hospital CHU Dinant Godinne UCL
NOT_YET_RECRUITINGYvoir, 5530, Belgium
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Other studies related to the condition(s) this trial covers.
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- Can brain scans reveal why stroke disrupts Two-Handed learning?