ADHD 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:
- You are male or female, aged between 18 and 75 years old (children aged 8–17 may also be eligible for the ADHD group specifically)
- You have normal vision, or your vision is corrected (for example, with glasses or contact lenses)
- You are covered by social security
- You are willing and able to sign a written consent form agre- If you are a minor, your legal guardian(s) must also give written consent
For people who have had a stroke and have a condition called hemispatial neglect (difficulty noticing things on one side):
- You had a stroke more than 1 month ago, with evidence of brain injury shown on a brain scan and by noticeable symptoms
- Your condition has been confirmed as hemispatial neglect and not a different vision problem (confirm with trial site)
For people who have had a stroke and have a condition called optic ataxia (difficulty reaching or pointing accurately):
- You had a stroke more than 1 month ago, with brain injury limited to a specific area called the parietal cortex, confirmed by an MRI scan
- You experience difficulties pointing or reaching accurately, either with your hand or toward objects on a specific side
For people with ADHD (Attention Deficit Hyperactivity Disorder):
- You have a formal ADHD diagnosis (either the inattentive type or the hyperactive/impulsive type) given by a neuropsychologist
- You do not have any learning disabilities alongside your ADHD
For healthy volunteers:
- You have no known neurological injury or condition
Who may not be able to join:
- You have difficulties that would prevent you from following the study requirements, such as neurological, psychiatric, sensory, or movement-related problems
- You are an adult who is under any form of legal protection (confirm with trial site)
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: Laure PISELLA, Centre de recherche de Neurosciences de Lyon (CRNL)
Phone: 4 72 91 34 05
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
error rate
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.