Clinical Trials in Belgium / NCT07826832
Recruiting Not applicable

Unimanual Versus Bimanual Motor Skill Learning in Acute and Chronic Stroke

NCT07826832 · tracked via the Priya Life Science Belgium tracker
Phase
Not applicable
Started
2026-05-18
Last updated
2026-09-17

Condition(s) studied

Acute StrokeChronic Stroke PatientHealthy Individuals (Controls)Stroke (Subacute)

Investigational drug(s) / intervention(s)

REAplan®Dextrain® Manipulandum

REAplan®: motor skill learning with the REAplan® rehabilitation robot, to be performed with one or two arms

Dextrain® Manipulandum: motor skill learning with the Dextrain® Manipulandum dexterity tool to be performed with on or two hands

Study summary

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.

Eligibility

Sex
ALL
Min age
40 Years
Max age
90 Years
Healthy volunteers
Accepted
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHU UCL Namur Yvoir Namur Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07826832 on ClinicalTrials.gov ↗ ← All trials in Belgium