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NCT05884762Recruiting

earlY Upper Limb Rehabilitation WIth EEG-Neurofeedback After Stroke

Source: ClinicalTrials.gov · Last updated 3 Mar 2026

Brief summary (registry, in English)

The aim of this study is to evaluate the effect of early rehabilitation treatment by electroencephalographic neurofeedback on upper limb motor function after stroke. Researchers will compare : Interventional group: electroencephalographic neurofeedback + traditional reference rehabilitation programme Control group: SHAM electroencephalographic neurofeedback + traditional reference rehabilitation programme

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
23 May 2023
Start date
20 Feb 2024
Primary completion date
Nov 2027
Lead sponsor
Rennes University Hospital
Diseases
Stroke
NCT number
NCT05884762

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 20 Feb 2024 to the primary completion date, Nov 2027
  • 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

  • Contraindication to MRI
    • pacemaker or implantable defibrillator,
    • neurosurgical clips,
    • cochlear implants,
    • intra-orbital or encephalic metallic foreign bodies,
    • stents placed less than 4 weeks ago and osteosynthesis devices placed less than 6 weeks ago,
    • claustrophobia. (Patients who have undergone thrombolysis or thrombectomy may be included in the study.)

Other illness

  • Stroke \< 1 week; in order not to be deleterious by starting active rehabilitation too early after immediate stroke
  • Aphasia with major comprehension impairment

Other

  • Ischemic or hemorrhagic brain stem and/or cerebellum involvement
  • Multiple strokes

Who the study is looking for

  • Unilateral ischaemic or haemorrhagic stroke
  • Adult (18-80 years), both sexes
  • Stroke \< 3 weeks
  • Upper limb deficit defined by Shoulder Abduction Finger Extension score \<5 measured during the 7 days following stroke; i.e., patients predicted to have incomplete recovery
  • No participation-limiting comprehension problems
  • With or without homonymous lateral hemianopia; with or without visuospatial hemineglect
  • Free, informed and written consent signed by the patient or a member of the patient's family (in the case of a patient who is able to understand the information and give consent but has motor difficulties resulting in an invalid signature).
  • Affiliated to french social security

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Rennes - CHU
Coordinator of this site? Confirm its status
RennesFranceRecruiting

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