NCT06212219Recruiting
Neurofeedback-EEG Rehabilitation Protocol on Motor Recovery in the Subacute Phase Post-stroke (CUSTOM-NF-STROKE)
Impact of Personalization of a Neurofeedback-EEG Rehabilitation Protocol on Motor Recovery in the Subacute Phase Post-stroke (CUSTOM-NF-STROKE)
Source: ClinicalTrials.gov · Last updated 29 May 2026
Brief summary (registry, in English)
Neurofeedback (NF) is a procedure for providing direct sensory feedback (in the form of visual, auditory or tactile stimulation) to a patient about their brain activity when performing a cognitive or motor task. This NF aims to allow the patient to become aware of this brain activity and thus learn to modulate it voluntarily in order to improve the performance obtained on the task. The aim of the study is to compare a "standard NF" procedure to a "personalized NF" procedure designed to optimize the level of patient acceptability based on the results obtained through these questionnaires.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 44 (estimated)
- First submitted
- 8 Jan 2024
- Start date
- 8 Jan 2024
- Primary completion date
- 31 Dec 2027
- Lead sponsor
- University Hospital, Toulouse
- Diseases
- Stroke
- NCT number
- NCT06212219
What you commit to
- Study type: Interventional
- Planned participants: 44
- From 8 Jan 2024 to the primary completion date, 31 Dec 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
- Factors hindering EEG acquisition (scalp pathology, abnormal cervico-cephalic movements, cranial metal implants)
Other illness
- Phasic disorder limiting comprehension corresponding to a Boston Diagnostic Aphasia Examination (BDAE) score \< 4
- Attentional disorder not allowing sufficient attention to be maintained for 1 hour
- History of known stroke with motor sequelae.
- Unstabilized epilepsy
Age
- Minors (age \< 18 years)
Other
- Known peripheral neurological pathology affecting the paretic upper limb.
- Other known central neurological pathology
- Refusal to participate in the study
- Protected patient: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision
- Pregnant, parturient, or breastfeeding patient
Who the study is looking for
- Man, woman, over 18 years old
- Motor deficit of the upper limb type of hemiplegia, secondary to a hemorrhagic or ischemic stroke authenticated by brain imaging (MRI or CT)
- Post-stroke patients in the subacute phase, between 15 days and 6 months after the stroke
- Correct or corrected vision allowing reading at a distance of 0 to 2m
- Ability to maintain a seated position for 1 hour
- Patient affiliated to a social security scheme or beneficiary of such a scheme
- Informed patient having signed consent
Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU de Toulouse Coordinator of this site? Confirm its status | Toulouse | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.