Brain scans and Decision-Making tasks aim to uncover OCD's hidden markers
NCT ID NCT03313622
First seen Jun 30, 2026 · Last updated Jul 01, 2026 · Updated 1 time
Summary
This study looks for brain-based markers (biomarkers) of obsessive-compulsive disorder (OCD) in people with severe, hard-to-treat symptoms. Participants complete decision-making tasks and are exposed to personal OCD triggers while their brain activity is recorded with EEG and their facial reactions are filmed. The goal is to better understand the brain circuits involved in OCD, which could eventually lead to more personalized treatments.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could identify measurable brain signals linked to OCD symptoms, paving the way for more targeted treatments.
- What could go wrong
- This is a small, early-stage observational study focused on discovery, not treatment. It may not yield clear or generalizable biomarkers.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2027
An estimate. Start dates often move.
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Potential subjects are patients diagnosed with OCD meeting the inclusion/exclusion criteria above.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of OCD * Non-pregnant if female * Minimum score of 16 on Y-BOCS * Ability to provide informed consent Exclusion Criteria: * Those not meeting inclusion criteria listed above * Lifetime diagnosis of psychotic disorders such as schizophrenia * Alcohol or substance abuse/dependence within 6 months, excluding nicotine * Deemed at high risk of suicidal behavior or impulsivity * Pregnant or plans to become pregnant in the next 24 months
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Get notified about this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Baylor College of Medicine
Houston, Texas, 77030, United States
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Brown University
Providence, Rhode Island, 02912, United States
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University of Pittsburgh
Pittsburgh, Pennsylvania, 15260, United States
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