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:
- You are a woman between 18 and 35 years old
- You have been diagnosed with restrictive-type anorexia nervosa according to standard medical guidelines (DSM-5)
- Your Body Mass Index (BMI) is between 15.0 and 18.5 (a measure of body weight relative to height)
- Your doctor considers you physically stable enough to take part in psychological and brain-related assessments
- You are willing to attend weekly therapy sessions (if placed in the therapy group) and complete assessments at the start and end of the trial
- You are able to give your own informed agreement to take part in the study
Who may not be able to join:
- You have ever been diagnosed with bulimia nervosa, binge-eating disorder, or any other eating disorder
- You currently have a serious mental health condition such as psychosis, bipolar disorder, or a substance use disorder
- You have a history of a neurological illness or a brain injury caused by trauma
- You have taken psychiatric medications in the last 6 weeks
- You have previously taken part in a structured Cognitive-Behavioral Therapy (CBT) programme specifically for an eating disorder
- You are currently pregnant
- You have vision or neurological difficulties that would interfere with brain and body measurement recordings (such as EEG, skin response, or eye-tracking tests) (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: Gökben Hızlı Sayar, Professor, Üsküdar University
Phone: 00905324732070
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 EEG P300 amplitude in response to body image stimuli; Change in Late Positive Potential (LPP) amplitude to body and food stimuli; Change in frontal alpha asymmetry during self-image viewing; Change in skin conductance response (SCR) to body and food stimuli; Change in fixation duration on weight-related body areas
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.