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NCT02006199 Clinical Trial

Effect of Mindfulness Based Treatment for Obsessive-compulsive Disorder

Obsessive-compulsive Disorder Clinical Trial

Official title:
Effect of Mindfulness Based Treatment for Obsessive-compulsive Disorder

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT02006199
Other study ID # 1306-076-498
Secondary ID
Status Withdrawn
Phase N/A
First received December 4, 2013
Last updated October 12, 2016
Start date October 2013
Est. completion date July 2014

Study information
Verified date December 2013
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Hypothesis of this study is that mindfulness meditation would decrease the severity of obsessive-compulsive symptoms.

Description:

Before and after 8 weeks of mindfulness program, We will measure Y-BOCS scores in OCD patients. As a control program, relaxation and psychoeducation will provided to OCD patients.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date July 2014
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender Both
Age group 17 Years to 55 Years
Eligibility Inclusion Criteria:

- obsessive-compulsive disorder

- age 17-55

Exclusion Criteria:

- currently undergoing Cognitive Behavioral Therapy, psychotherapy

- other medical disease

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• mindfulness meditation
8 weeks of mindfulness meditation specified for OCD patient

Locations
Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Other HAM-D 8 weeks No
Primary Yale-Brown Obsessive compulsive scores 8 weeks No
Secondary Neurocognitive profile (emotion-memory task) 8 weeks No
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