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Effect of Mindfulness Based Treatment for Obsessive-compulsive Disorder

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ClinicalTrials.gov Identifier: NCT02006199
Recruitment Status : Withdrawn (Withdrawal of the administrative reason)
First Posted : December 10, 2013
Last Update Posted : October 14, 2016
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
Hypothesis of this study is that mindfulness meditation would decrease the severity of obsessive-compulsive symptoms.

Condition or disease Intervention/treatment
Obsessive-compulsive Disorder Behavioral: mindfulness meditation

Detailed 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.

Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Effect of Mindfulness Based Treatment for Obsessive-compulsive Disorder
Study Start Date : October 2013
Estimated Primary Completion Date : July 2014
Estimated Study Completion Date : July 2014

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Arms and Interventions

Arm Intervention/treatment
Experimental: relaxation with psychoeducation
after 8 weeks of relaxation with psychoeducation. subject take part in 8 weeks of the mindfulness meditation program
Behavioral: mindfulness meditation
8 weeks of mindfulness meditation specified for OCD patient
Experimental: meditation
8 weeks of mindfulness meditation
Behavioral: mindfulness meditation
8 weeks of mindfulness meditation specified for OCD patient


Outcome Measures

Primary Outcome Measures :
  1. Yale-Brown Obsessive compulsive scores [ Time Frame: 8 weeks ]

Secondary Outcome Measures :
  1. Neurocognitive profile (emotion-memory task) [ Time Frame: 8 weeks ]

Other Outcome Measures:
  1. HAM-D [ Time Frame: 8 weeks ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   17 Years to 55 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • obsessive-compulsive disorder
  • age 17-55

Exclusion Criteria:

  • currently undergoing Cognitive Behavioral Therapy, psychotherapy
  • other medical disease
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02006199


Locations
Korea, Republic of
Seoul National University Hospital
Seoul, Korea, Republic of, 110-744
Sponsors and Collaborators
Seoul National University Hospital
Investigators
Principal Investigator: Jun Soo Kwon, MD phD Seoul National University College of Medicine
More Information

Responsible Party: Seoul National University Hospital
ClinicalTrials.gov Identifier: NCT02006199     History of Changes
Other Study ID Numbers: 1306-076-498
First Posted: December 10, 2013    Key Record Dates
Last Update Posted: October 14, 2016
Last Verified: December 2013
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Seoul National University Hospital:
obsessive-compulsive disorder
mindfulness
meditation

Additional relevant MeSH terms:
Disease
Compulsive Personality Disorder
Obsessive-Compulsive Disorder
Pathologic Processes
Personality Disorders
Mental Disorders
Anxiety Disorders