NCT07826832Recruiting
Unimanual Versus Bimanual Motor Skill Learning in Acute and Chronic Stroke
Comparison of Unimanual Versus Bimanual Motor Skill Learning (Proximal and Distal) After Stroke by Means of Robotics (REA²Plan® and Dextrain®) and Multimodal Brain Imaging (VLSM, DTI, NODDI, DIAMOND)
Source: ClinicalTrials.gov · Last updated 17 Sept 2026
Brief summary (registry, in English)
To test the capacity of healthy individuals, chronic and acute stroke patients to learn and retain a complex unimanual or bimanual motor skill, trained on the neurorehabiliation robot REAplan® et the Dextrain® device. The goals are (1) to compare head-to-head bimanual versus unimanual motor learning (in the proximal and distal upper limb, UL) during the acute - early subactue stage of stroke with robotics and (2) to identify the neural substrates associated with (and deficits in) unimanual versus bimanual motor control (proximal and distal) after stroke by means of multimodal brain imaging.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- First submitted
- 8 Sept 2026
- Start date
- 18 May 2026
- Primary completion date
- 31 Dec 2028
- Lead sponsor
- University Hospital of Mont-Godinne
- Diseases
- Stroke
- NCT number
- NCT07826832
What you commit to
- Study type: Interventional
- Planned participants: 200
- From 18 May 2026 to the primary completion date, 31 Dec 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- drug/alcohol abuse
- medical history with a previous stroke/relevant neurological deficit
- drug/alcohol abuse
Other illness
- multiple stroke/dementia/psychiatric condition
- HEALTHY INDIVIDUALS
- psychiatric condition/dementia
Other
- \[for acute paitents\] "classical" contre-indication to MRI (non-MR-compatible pacemaker, pregnancy, non-MR-compatible implanted devices, claustrophobia, etc ...)
- difficulty in understanding or executing commands
- severe aphasia/cognitive deficits interfering with study
- inability to complete the tasks (i.e. full paralysis of the arm)
- "classical" contre-indication to MRI (non-MR-compatible pacemaker, pregnancy, non-MR-compatible implanted devices, claustrophobia, etc ...)
- having already used the robotic devices
Who the study is looking for
- 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
- 40-90 years
Criteria the registry did not label
- STROKE PATIENTS
Age in the registry: 40 years to 90 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Chu Ucl Namur Coordinator of this site? Confirm its status | Yvoir | Belgium | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.