- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05195476
Neural Correlates of Compulsivity
May 3, 2024 updated by: Amy Rapp, Columbia University
This study aims to collect data from individuals with obsessive-compulsive disorder (OCD) and healthy controls in order to clarify how learning strategies are employed differently by individuals with compulsive psychopathology and healthy individuals.
Behavioral and electroencephalogram (EEG) data will be collected during one experimental reinforcement learning tasks from participants diagnosed with OCD (n = 30) and healthy controls (n = 30).
Computational modeling, an advanced data analytic approach that can directly link neural measures with behavior, will be used to quantify learning processes.
These parameters then will be related to measures of neural events obtained using EEG, a neuroimaging method that has high temporal resolution, to test for evidence of neurocognitive alterations.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Learning and decisions making are thought to be directed by multiple parallel cognitive systems.
These systems account for automatic, inflexible responding to stimuli, as well as more deliberate, effortful representations of relationships in an environment.
It has long been suggested than an imbalance in these cognitive control systems explains the emergence of compulsivity, a trait in which behaviors persist despite adverse outcomes.
Compulsivity is a characteristic of a number of psychological disorders, however, current theories of how abnormalities in cognitive systems involved in learning and decision making lead to the onset of these disorders remain incomplete.
Study Type
Observational
Enrollment (Actual)
41
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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New York
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New York, New York, United States, 10032
- New York State Psychiatric Institute
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 50 years (Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Individuals diagnosed with OCD and healthy controls
Description
Inclusion Criteria:
- Between 18-50 years of age
- English-speaking
- Capacity to provide informed consent
- Primary diagnosis of OCD with at least moderate severity
Exclusion Criteria:
- Current or lifetime history of psychiatric disorders other than OCD that may increase the risk of participation
- History of any significant medical condition that may increase the risk of participation
- Alcohol or substance use disorder in the past year
- Exposure and response prevention for OCD within the last six weeks
- Currently taking psychotropic medication
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Individuals diagnosed with OCD
|
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Healthy controls
Individuals who have not been diagnosed with any psychiatric disorders
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neural Activity
Time Frame: One-time study visit
|
EEG will be recorded while participants complete computerized reinforcement learning tasks at one study visit
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One-time study visit
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Amy Rapp, PhD, Columbia University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 17, 2021
Primary Completion (Actual)
February 28, 2024
Study Completion (Actual)
February 28, 2024
Study Registration Dates
First Submitted
January 4, 2022
First Submitted That Met QC Criteria
January 4, 2022
First Posted (Actual)
January 19, 2022
Study Record Updates
Last Update Posted (Actual)
May 6, 2024
Last Update Submitted That Met QC Criteria
May 3, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 7867
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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