OCD 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 between 18 and 65 years old
- You have been diagnosed with one of the following conditions: Obsessive-Compulsive Disorder (OCD), Body Dysmorphic Disorder (BDD), Illness Anxiety Disorder, or Somatic Symptom Disorder (but not the type that mainly involves pain)
- You have strong beliefs or worries related to your condition that reach a certain level of intensity, as measured by a specific assessment tool (confirm with trial site)
- If you take psychiatric medication, your dose or type has not changed recently
- You are able to understand the study and agree to take part on your own
Who may not be able to join:
- You have certain mental health or physical health conditions — for example, dizziness problems or a history of ear surgery — that could make taking part unsafe
- You are currently pregnant or breastfeeding
- You are currently using, or have recently used, recreational drugs or alcohol in a way that may be a concern
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: Peter J van Roessel, MD, PhD, Stanford University
Phone: 650-723-4095
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 clinical insight as measured by the Brown Assessment of Beliefs (BABS).
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.