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NCT04171856Recruiting

Exploring Motor Learning in Acute Stroke Through Robotics

Source: ClinicalTrials.gov · Last updated 12 Aug 2026

Brief summary (registry, in English)

The acute phase of stroke is characterized by an enhancement of neural plasticity which supports rapid motor recovery. It is unclear whether acute stroke patients can acquire new motor skills with their affected upper limb. The aims of this research program are: 1. To test the capacity of acute stroke patients (\< 21 days) to learn and retain a complex unimanual motor skill. 2. To explore whether acute stroke to different brain regions (quantified with brain MRI) induces specific deficits in motor skill learning. 3. To compare acute stroke patients with healthy individuals and with chronic stroke patients.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
245 (estimated)
First submitted
12 Nov 2019
Start date
1 Jan 2020
Primary completion date
1 May 2030
Lead sponsor
University Hospital of Mont-Godinne
Diseases
Stroke
NCT number
NCT04171856

What you commit to

  • Study type: Interventional
  • Planned participants: 245
  • From 1 Jan 2020 to the primary completion date, 1 May 2030
  • 2 sites 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
  • Alcohol / drug addiction
  • medical history with a previous stroke/neurological deficit
  • drug/alcohol abuse
  • drug/alcohol abuse

Other illness

  • multiple strokes / dementia / psychiatric condition
    • PATIENTS WITH TRANSIENT GLOBAL AMNESIA:
    • Clinical diagnosis, criteria of Hodge \& Warlow (1990):
  • Psychiatric disorders
  • psychiatric condition/ dementia
    • CHRONIC STROKE PATIENTS:
  • multiple strokes / dementia / psychiatric condition

Other

  • " classical " contre-indication to MRI (non-MR-compatible pacemaker, pregnancy, non-MR-compatible implanted devices, claustrophoby, etc ...)
  • difficulty in understanding or executing commands
  • severe aphasia / cognitive deficits interfering with study
  • inability to voluntarily move the affected arm (i.e. complete paralysis of the arm)
  • 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
  • Severe aphasia / cognitive deficits interfering with study
  • Exclusion criteria related to MRI
    • HEALTHY INDIVIDUALS:
  • difficulty in understanding or executing commands
  • severe aphasia / cognitive deficits interfering with study
  • inability to voluntarily move the affected arm (i.e. complete paralysis of the arm)

Who the study is looking for

  • acute stroke (\> 21 days)
  • aged 18-90 years
  • with a stroke lesion on brain imaging
  • Transient global amnesia
  • 8-90 years old
  • Be able to perform 3 consecutive sessions on a rehabilitation robot
  • 18-90 years
  • chronic stroke (\>6 months)
  • aged 18-90 years
  • with a stroke lesion on brain imaging

Criteria the registry did not label

  • ACUTE STROKE PATIENTS:

Age in the registry: 18 years to 90 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Chu Ucl Namur
Coordinator of this site? Confirm its status
YvoirBelgiumRecruiting
University Hospital CHU Dinant Godinne UCL
Coordinator of this site? Confirm its status
YvoirBelgiumNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.