Fact CheckerSign in

NCT04847089Completed

Motor Imagery BCI Rehabilitation After Stroke

Motor Imagery and Real-time Feedback in Stroke Rehabilitation

Source: ClinicalTrials.gov · Last updated 22 Dec 2025

Brief summary (registry, in English)

This research project will investigate motor imagery training in stroke rehabilitation during which patients receive feedback in real time from their brain activity measured with ElectroEncephaloGraphy (EEG). The investigators hypothesize that the feedback training allows to internally stimulate brain motor networks in order to promote functional recovery of the hand.

Status (registry)
Completed
Study type
Interventional
Enrollment
16 (actual)
First submitted
14 Apr 2021
Start date
14 Apr 2022
Primary completion date
1 Jul 2025
Lead sponsor
Mälardalen University
Diseases
Stroke
NCT number
NCT04847089

What you commit to

  • Study type: Interventional
  • Participants enrolled: 16
  • From 14 Apr 2022 to the primary completion date, 1 Jul 2025
  • 3 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

  • If the research person is regularly treated with botulinum toxin in the upper extremity, 3 weeks should have passed before the first baseline assessment.
  • metal implants in the brain/skull cochlear implants,

Other illness

  • other neurological or musculoskeletal disease/injury, or contagious disease.
  • current or history of epilepsy,
  • any implanted neurostimulator, cardiac pacemaker or cardiac implants of metal, infusion device,
  • any other neurological disorder,
  • current or history of severe psychiatric disorder with need for pharmacological treatment

Other

  • severe hearing or visual impairments,
  • pregnancy,

Who the study is looking for

  • \> 6 months since first time stroke onset and with remaining hemiparesis in upper extremity; able to participate fully in the intervention, able to perform Functional Magnetic Resonance Imaging (fMRI); able to passively extend the wrist 15 degrees and extend fingers fully with a neutral position of the wrist.
  • In addition, participants need to be able to voluntarily control the power of their grip when requested according to the Visuomotor force tracking method and/or according to the clinical assessment of a therapist (while holding the patient´s hand). According to the Fugl- Meyer Upper Extremity (UE) scale participants should accomplish \<14 points on the hand subscale and \<2 points in finger flexion and extension (C) in addition to \< 47 points on the total motor score (equivalent to moderate disability in the upper extremity.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of rehabilitation medicine at Danderyd University
Coordinator of this site? Confirm its status
StockholmSwedenUnknown status
Stockholn University Brain Imaging Centre
Coordinator of this site? Confirm its status
StockholmSwedenUnknown status
Sweden Mälardalen University
Coordinator of this site? Confirm its status
VästeråsSwedenUnknown status

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