Stroke Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
For patients who have had a stroke or brain bleed:
Who might be able to join this trial:
- People aged 18 or older at the time of joining the trial
- People who are covered by a social security system, Universal Health Coverage, or an equivalent health coverage scheme
- People who had an ischemic stroke (blocked blood vessel in the brain) or a brain bleed more than 6 months ago, with no upper time limit on how long ago it occurred
- People who have some weakness or movement difficulty in their upper limb as measured by a specific assessment tool called the ARAT scale, and who are able to grip and press on a tablet device
- People whose stroke or brain bleed did not affect the specific area of the brain that controls hand movement (called the hand knob area of the motor cortex)
Who may not be able to join:
- Women who are pregnant or breastfeeding
- People who have complete paralysis of the affected hand with no movement at all
- People with conditions that are life-threatening or that could make it difficult to complete follow-up appointments during the study
- People with certain medical implants or devices that are not compatible with MRI scans or a type of brain stimulation used in the trial (such as ferromagnetic surgical clips, certain eye implants, metal objects in the eye or nervous system, cochlear implants, brain or heart stimulators, or a craniotomy scar)
- People who are currently taking part in another medical research study focused on motor or overall recovery, or who are in an exclusion period from a previous biomedical study
For healthy volunteers:
Who might be able to join this trial:
- People aged 18 or older at the time of joining the trial
- People who are covered by a social security system, Universal Health Coverage, or an equivalent health coverage scheme
Who may not be able to join:
- Women who are pregnant or breastfeeding
- People with conditions that are life-threatening or that could make it difficult to complete follow-up appointments during the study
- People with certain medical implants or devices that are not compatible with MRI scans or a type of brain stimulation used in the trial (such as ferromagnetic surgical clips, certain eye implants, metal objects in the eye or nervous system, cochlear implants, brain or heart stimulators, or a craniotomy scar)
- People who are currently taking part in another biomedical research study, or who are in an exclusion period from a previous biomedical study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Charlotte ROSSO, MD PHD, Institut National de la Santé Et de la Recherche Médicale, France
Phone: +33142162103
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
change in activation in the primary motor cortex and cerebellum using functional magnetic Resonance
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.