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Cognitive Behavioral Therapy Plus Drug Treatment for Obsessive Compulsive Disorder

Not Applicable
Completed
Conditions
Obsessive-Compulsive Disorder
Interventions
Behavioral: Exposure and Ritual Prevention (Cognitive Behavioral Therapy)
Behavioral: Stress Management Therapy (Cognitive Behavior Therapy)
Registration Number
NCT00045903
Lead Sponsor
New York State Psychiatric Institute
Brief Summary

This study will evaluate the effectiveness of two cognitive behavioral therapies (CBTs) in treating obsessive compulsive disorder (OCD) in patients who are taking medication but still have residual symptoms.

Detailed Description

Participants remain on their current OCD medication and are randomly assigned to receive one of two CBTs: exposure and ritual prevention or stress management therapy. Exposure and ritual prevention involves imaginal and in-vivo exposure and requires that participants refrain from ritualizing. Stress management involves relaxation, assertiveness training, and structured problem-solving. Therapy occurs twice per week for 2 months. Participants are assessed verbally by an independent evaluator and are asked to complete self-rating forms. Patients who respond are followed for up to 1 additional year. Participants continue to take the same medication and the same monthly therapy for the first 6 months of follow-up. During the second 6 months of follow-up, participants discontinue therapy but continue taking the same medication.

For information on a related study, please follow this link:

http://clinicaltrials.gov/show/NCT00389493

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
136
Inclusion Criteria
  • Obsessive-Compulsive Disorder (OCD) diagnosis
  • Currently taking a serotonin reuptake inhibitor (SRI, i.e. clomipramine, fluoxetine, fluvoxamine, paroxetine, sertraline, or citalopram) for OCD
Exclusion Criteria
  • Medical or psychiatric conditions that would make participation in the study hazardous
  • Intensive cognitive-behavioral therapy while on an adequate dose and duration of an SRI for OCD

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Exposure and Ritual PreventionExposure and Ritual Prevention (Cognitive Behavioral Therapy)Exposure and Ritual Prevention Therapy
Stress ManagementStress Management Therapy (Cognitive Behavior Therapy)Stress Management Therapy
Primary Outcome Measures
NameTimeMethod
Obsessive-compulsive symptoms measured at Month 22 months
Secondary Outcome Measures
NameTimeMethod
General functioning measured at Month 22 months

Trial Locations

Locations (2)

University of Pennsylvania Center for the Treatment and Study of Anxiety

🇺🇸

Philadelphia, Pennsylvania, United States

New York State Psychiactic Institute, Anxiety Disorders Clinic

🇺🇸

New York, New York, United States

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