Efficacy of Exposure and Response Prevention(ERP) and SSRIs in Chinese OCD Patients
Obsessive-Compulsive Disorder, Anxiety Disorders, Mental Disorders
About this trial
This is an interventional treatment trial for Obsessive-Compulsive Disorder focused on measuring Cognitive Behavior Therapy, Exposure and Response/Ritual Prevention, Selective Serotonin Reuptake Inhibitors, Psychotherapy, Pharmacotherapy, Citalopram, Fluoxetine, Paroxetine, Sertraline, Fluvoxamine, fMRI, Stop Signal Task
Eligibility Criteria
Inclusion Criteria:
- Having been diagnosed with primary OCD as defined by the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-) criteria;Cleaning or checking as primary OCD symptoms
- Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) score of ≥ 16
- Never receiving adequate treatment or stop receiving treatment for at least 8 weeks
- Having an education degree of high school or above
- Accepting to participate in the study
Exclusion Criteria:
- Having significant medical illnesses that would interfere with the conduct of the study
- Clinically significant abnormal laboratory finding
- Having comorbid psychiatric conditions according to the criteria set forth in the DSM-IV(administered by the Mini-International Neuropsychiatric Interview (MINI))
- The current OCD symptoms are too severe that the patient cannot finish the evaluation or receive the ERP
- Being currently at risk for suicide
- Being pregnant or having the intention to be pregnant before the end of the study
- A history of having inadequate response to adequate SSRIs or CBT treatment
- Subjects who are unable to undergo the MRI
Sites / Locations
- Shanghai Mental Health Center
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Selective Serotonin Reuptake Inhibitor
Exposure and Response Prevention
In this group,routine treatment strategies will be used for patients. Any one of the SSRIs including fluoxetine, citalopram, paroxetine, sertraline, fluvoxamine ,which are approved in the treatment of OCD by SFDA, may be used for patients who are randomized to this treatment arm. The dosage depends on clinician's judgement ,but not over the maximum tolerated dosage.
Exposure and Response Prevention Structured protocol described by Foa et al., 2012 Patients will attend eight 1-h sessions,once a week. Benzodiazepine will be used when necessary.