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 18 years of age or older
- You are receiving treatment at an outpatient addiction department at the University Hospital of Brest, Nantes, or Tours, and you have been diagnosed with both ADHD and a behavioural addiction
- You are enrolled in the French social security system
- If you are currently taking methylphenidate (a medication for ADHD): your dose has not changed in the past three months
- If you are not currently taking methylphenidate: there are no plans to start you on this medication in the next three months
Who may not be able to join:
- People who have a psychotic disorder, as assessed by their doctor
- Women who are pregnant or breastfeeding
- People who are under legal guardianship or a similar form of protected supervision
- People who are under court-ordered legal protection
- People who are currently deprived of their liberty (for example, in prison)
- People who are not considered suitable for Cognitive Behavioural Therapy (CBT), for example due to cognitive difficulties or hearing problems (confirm with trial site)
- People who are physically unable to take part in CBT sessions, for example because they do not have access to a telephone or know they will be unavailable (confirm with trial site)
- People who have difficulty understanding written questionnaires, including those who cannot read
- People who are already taking part in another clinical study involving a different psychological therapy or medication that could affect the results of this trial
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: Servane BARRAULT, Dr, CHRU de Tours
Phone: (+33)2.47.47.91.91
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
Retention rate; Adhesion; Adhesion
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.