Clinical trial Recruiting at 1 site Interventional Ages 18 to 55

Using EEG and computational models to better understand compulsivity in OCD

Official title: Dissecting Neurocognitive Components of Compulsivity Using Computational Modeling and EEG

Run by Icahn School of Medicine at Mount Sinai · NCT07011901 · Data updated 2026-11-12

This project will test whether combining EEG recordings with computational cognitive models can reveal distinct brain and behavior patterns in adults with OCD compared to adults without OCD.

Quick facts

Study typeInterventional
Ages18 Years to 55 Years
SexAll
Enrollment100 (estimated)
SponsorIcahn School of Medicine at Mount Sinai
Academic / other
Locations1 site (New York, New York)
StatusRecruiting
StartedJuly 9, 2025
Main results expectedMarch 31, 2030
Study endsMarch 31, 2030
Registry record updatedNovember 2, 2026
Trial IDNCT07011901 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are English-speaking, right-handed adults aged 18–55 with a current OCD diagnosis who can provide consent and meet medication and behavioral treatment washout criteria.

Probably not a fit

People with recent psychiatric medication or behavioral treatment for OCD, certain comorbid psychiatric diagnoses, non–English speakers, left-handed individuals, minors, or those unable to attend in-person visits at the study site are unlikely to qualify and may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This research will enroll 100 participants—50 adults diagnosed with OCD and 50 healthy controls—and collect behavioral, clinical, and EEG data during cognitive tasks. Investigators will apply theory-driven computational models to link task behavior and EEG signals to multiple neurocognitive subcomponents of compulsivity beyond the simple habit versus goal-directed framework. The protocol includes exposure and response prevention components alongside neurophysiological recording to connect treatment-relevant processes with neural markers. The goal is to identify neurocognitive profiles that could ultimately support more personalized treatment approaches for people with OCD.

Why it matters

Potential benefit: If successful, the work could identify markers that help match people with OCD to treatments that are most likely to work for their specific brain–behavior profile.

How similar studies have gone: Previous work using EEG and computational modeling has shown promising findings in OCD and related compulsivity research, but combining these methods to define clinically useful subtypes is still relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Participants must be:

* between the ages 18-55 years old
* English-speaking
* right-handed
* able to provide consent

Exclusion Criteria:

Individuals diagnosed with OCD will be excluded if:

* they meet diagnostic criteria for certain other psychiatric disorders
* are taking psychiatric medication or have received behavioral treatment for OCD within a certain timeframe
* if it is unsafe for them to participate in research

Healthy control participants will be excluded if:

* they have a current psychiatric disorder
* a lifetime history of certain psychiatric disorders
* are taking psychiatric medication or have in the past
* have a parent or sibling who has been diagnosed with OCD
* if it is unsafe for them to participate in research

Where it's running

  • Icahn School of Medicine at Mount Sinai
    New York, New York, United States
    Recruiting

Study contacts

  • Principal investigator: Amy Rapp, PhD — Icahn School of Medicine at Mount Sinai
  • Study coordinator: Amy Rapp, Ph.D.
  • Email: OCDResearch@mssm.edu
  • Phone: 212-241-5288

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.