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
Who might be able to join this trial:
- People who are male or female and aged between 18 and 79 years old
- People who have had an ischemic stroke (caused by a blockage), a hemorrhagic stroke (caused by bleeding in the brain), or a Transient Ischemic Attack (a brief, temporary stroke-like episode with a severity score of 4 or higher on a standard risk scale) within the last 15 days, confirmed by a brain scan (CT or MRI)
- People who are already scheduled to return to the Bordeaux Hospital stroke unit for their standard 3-month follow-up appointment after their stroke
- People whose stroke symptoms are below a certain level of severity, as measured by a standard medical scale used by neurologists (score below 15 on the NIHSS)
- People who have a level of independence in daily life at or below a certain threshold on a standard disability scale (modified Rankin scale score of 4 or less)
- People who do not have severe problems with thinking or memory, as assessed by the treating neurologist
- People who have signed a written consent form agreeing to take part
- People who are covered by the French National Health Insurance
- For a specific part of the study focused on a digital health device: people who are able to use a smartphone and live in an area with internet access
Who may not be able to join:
- People who have had a specific type of brain bleed called a subarachnoid hemorrhage, or who have dementia or another neurological condition
- People with severe difficulty speaking or understanding language, or severe vision problems that would interfere with completing the study assessments
- People whose physical or mental health is severely affected in a way that the neurologist believes would make it difficult to participate
- People who are pregnant or breastfeeding
- People who are not able to read French
- People who are under a legal protection order or who are not able to personally give their own consent to participate
- People who are already taking part in another study that changes how their medical follow-up is managed
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: Igor Sibon, University Hospital, Bordeaux
Phone: 05 56 79 55 20
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
Organization Alcohol, Smoking and Substance Involvement Screening Test (ASSIST); Organization Alcohol, Smoking and Substance Involvement Screening Test (ASSIST); Addiction Severity Index - Lite version (ASI); modified Yale Food Addiction Scale 2.0 (mYFAS 2.0); modified Yale Food Addiction Scale 2.0 (mYFAS 2.0); Fagerström Test for Nicotine Dependence (FTND) Score; Fagerström Test for Nicotine Dependence (FTND) Score; Fagerström Test for Nicotine Dependence (FTND) Score; Fagerström Test for Nicotine Dependence (FTND) Score; Alcohol Use Disorder Identification Test (AUDIT) Score; Alcohol Use Dis...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.