Robots and brain scans probe how stroke survivors relearn arm skills

NCT ID NCT07826832

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Recruiting now This study
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The trial has finished. Results may not be published yet.
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Cancelled before anyone took part.

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First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time

Summary

Researchers are studying how well people who have had a stroke learn a complex arm and hand skill when they train with one arm versus both arms. Participants include healthy volunteers, people in the early days after a stroke, and people more than six months past a stroke. They practice on two rehabilitation robots, the REAplan and the Dextrain, while brain scans map the areas involved in arm control. The goal is to understand which training approach suits different types of stroke damage.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Motor skill training with the REAplan rehabilitation robot and the Dextrain dexterity device
What this could lead to
If the approach works, it could help therapists choose whether to train one arm or both arms after a stroke, and guide how rehabilitation is matched to each patient's brain injury.
What could go wrong
This is an observational comparison, not a treatment trial, so it may not show which training method is better. Results from 200 people may not apply to every stroke survivor, and brain imaging findings may not translate into better recovery.

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Study facts

What this study's own registry entry says, in plain language.

Phase

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

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2026

Expected to finish

Dec 2031

An estimate. End dates often move.

Lead sponsor

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

40 to 90 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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.

STROKE PATIENTS Inclusion Criteria: * acute stroke (between day 2 and day 21 post-stroke) or chronic stroke (\>6 mois) * aged 40-90 years * with a single demonstrated stroke (ischemic or hemorrhagic) lesion on brain imaging Exclusion Criteria: * \[for acute paitents\] "classical" contre-indication to MRI (non-MR-compatible pacemaker, pregnancy, non-MR-compatible implanted devices, claustrophobia, etc ...) * difficulty in understanding or executing commands * drug/alcohol abuse * severe aphasia/cognitive deficits interfering with study * inability to complete the tasks (i.e. full paralysis of the arm) * multiple stroke/dementia/psychiatric condition HEALTHY INDIVIDUALS Inclusion Criteria: * 40-90 years Exclusion Criteria: * "classical" contre-indication to MRI (non-MR-compatible pacemaker, pregnancy, non-MR-compatible implanted devices, claustrophobia, etc ...) * medical history with a previous stroke/relevant neurological deficit * drug/alcohol abuse * psychiatric condition/dementia * having already used the robotic devices

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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Contacts and locations

Locations

  • CHU UCL Namur

    RECRUITING

    Yvoir, Namur, 5530, Belgium

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