Obsessive-Compulsive Disorder Clinical Trial
Official title:
Control & Reward Circuits as Targets for Repetitive Thoughts and Behaviors
Verified date | March 2019 |
Source | New York State Psychiatric Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to examine the brain functioning of OCD patients and healthy controls before and after treatment with Exposure and Response Prevention (EXRP) therapy.
Status | Completed |
Enrollment | 80 |
Est. completion date | August 2018 |
Est. primary completion date | June 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 55 Years |
Eligibility |
Inclusion Criteria for Patients: - Male and females with OCD aged 18-55 - Diagnostic and Statistical Manual of Mental Disorders (DSM-5) Diagnosis of OCD - Not on psychotropic medication Exclusion Criteria for Patients: - Presence of metallic devices or dental braces in the body that are contraindicators for MR imaging - Comorbid psychiatric conditions that significantly elevate the risk of study participation (e.g. psychotic disorders, bipolar disorder, evidence of dementia or other cognitive disorder, suicidality) - Unstable medical conditions that need attention and would make participation in the study unsafe (e.g. very high blood pressure) - Use of psychotropic medication - Females who are pregnant or post-menopausal Inclusion Criteria for Healthy Volunteers - Male and females aged 18-55 Exclusion Criteria for Healthy Volunteers - Presence of metallic devices or dental braces in the body that are contraindicators for MR imaging - Any psychiatric diagnosis - Use of psychotropic medication - Diagnosis of OCD in a first degree relative - Females who are pregnant or post-menopausal - Unstable medical conditions that need attention and would make participation in the study unsafe (e.g. very high blood pressure) |
Country | Name | City | State |
---|---|---|---|
United States | NY State Psychiatric Institute | New York | New York |
Lead Sponsor | Collaborator |
---|---|
New York State Psychiatric Institute |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline in brain activation (fMRI) and fractional anisotropy (Diffusion tensor imaging) after therapy | Baseline & approximately 10 weeks later | ||
Secondary | Change in reaction times and correct responses on Stop signal reaction time task | Baseline and approximately 10 weeks later, at second scan |
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