Actively Recruiting

Phase Not Applicable
Age: 18Years - 90Years
All Genders
Healthy Volunteers
NCT05760846

Bimanual Motor Skill Learning in Acute Stroke

Led by University Hospital of Mont-Godinne · Updated on 2024-12-16

160

Participants Needed

2

Research Sites

284 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The subacute phase of stroke provides a window into how a lesion perturbs sensorimotor functions prior to reorganisation driven by plasticity and neurorehabilitation. The recovery from motor impairment has been extensively studied, but it is currently unknown whether motor skill learning (MSkL) is enhanced or impaired during acute stroke, especially bimanual motor skill learning (bim-MSkL), which likely requires more motor-attentional-cognitive resources than unimanual MSkL. The goals of this project are: to determine the neural substrates critical to achieve proximal and distal bimanual motor skill learning (bim-MSkL) by specifying whether (sub)acute stroke to different brain areas (cortical and subcortical) induce specific deficits in bimanual and/or distal bim-MSkL, which behavioral components are involved in bim-MSkL, and whether damage to the motor, sensory and inter-hemispheric pathways specifically impairs proximal and/or distal bim-MSkL.

CONDITIONS

Official Title

Bimanual Motor Skill Learning in Acute Stroke

Who Can Participate

Age: 18Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Acute stroke less than 21 days old
  • Age between 18 and 90 years
  • Confirmed ischemic or hemorrhagic stroke lesion on brain imaging
  • Healthy individuals aged 18 to 90 years (for control group)
Not Eligible

You will not qualify if you...

  • Contraindications to MRI such as non-MR-compatible pacemaker, implanted devices, pregnancy, or claustrophobia
  • Difficulty understanding or executing commands
  • Drug or alcohol abuse
  • Severe aphasia or cognitive deficits interfering with the study
  • Inability to complete tasks due to paralysis of the arm
  • Multiple strokes, dementia, or psychiatric conditions
  • History of previous stroke or relevant neurological deficit (for healthy controls)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

CHU UCL Namur

Yvoir, Namur, Belgium, 5530

Actively Recruiting

2

University Hospital CHU Dinant Godinne UCL

Yvoir, Belgium, 5530

Actively Recruiting

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Research Team

Y

Yves Vandermeeren, MD, PhD

CONTACT

C

Coralie van Ravestyn, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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