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Exposure and Response Prevention Therapy for Obsessive-compulsive Disorder

Obsessive-Compulsive Disorder Clinical Trial

Official title:
Exposure and Response Prevention Therapy for Obsessive-compulsive Disorder

Clinical Trial Summary

The purpose of this research study is to evaluate whether Exposure and Response Prevention Therapy (ERP) can help adults with obsessive-compulsive disorder (OCD) in China following a training of professionals and ongoing consultation.

Clinical Trial Description

The purpose of this research study is to evaluate whether Exposure and Response Prevention Therapy (ERP) can help adults with obsessive-compulsive disorder (OCD) in China following a training of professionals and ongoing consultation.The treatment time for each participant is approximately 12 weeks. This includes the time between the referral and the beginning of treatment, the treatment sessions, and the 1-month follow-up time. Therapy sessions will take place twice per week for 15 sessions total and last about 90 minutes each. In addition to the therapy sessions, participants will have 3 separate assessments. These assessments will occur (1) right after they agree to participate in the study, (2) immediately after ERP ends, and (3) 1 month after ERP ends. The assessments will take about 1 ½ hours each. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02602886
Study type Interventional
Source Ruijin Hospital
Contact ChenCheng Zhang, MD
Phone 18217122884
Email i@cczhang.com
Status Recruiting
Phase N/A
Start date November 2016
Completion date December 2017
View Details
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