Eating Disorders 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:
- Women between 18 and 60 years old (including age 60)
- Right-handed individuals
- For patients only: have been diagnosed with Binge Eating Disorder according to standard medical guidelines
- Covered by French social security or a related health insurance scheme
- Willing to participate in the study (no formal consent form required, but must not object to taking part)
Who may not be able to join:
For healthy volunteers only:
- Currently have an eating disorder or any other mental health condition
- Have previously had weight-loss (bariatric) surgery
For everyone (both patients and healthy volunteers):
- Have a rare form of obesity caused by a genetic condition or syndrome
- Have a specific addiction, whether to substances (such as drugs or alcohol) or certain behaviours
- Have a neurological condition, or a history of stroke or head injury
- Have skin lesions, wounds, or a skin condition in the areas where monitoring devices would need to be placed
- Have any serious ongoing or sudden illness (other than the condition being studied), or take any medication that could affect the study results
- Are unable to follow the requirements of the study
- Are considered unlikely to cooperate with the study, in the investigator's judgement
- Are unable to speak or read French
- Are currently pregnant or breastfeeding
- Are under a court or government order restricting their freedom, receiving compulsory psychiatric treatment, or are living in a health or social care institution for reasons unrelated to research (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: AMSALLEM Anne-Cécile, MD, CHU de Besançon
Phone: +33363082216
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
Measurement of prefrontal cortex activity using functional near-infrared imaging (fNIRS).
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.