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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01522287
Other study ID # R43MH090612
Secondary ID
Status Completed
Phase Phase 1
First received January 23, 2012
Last updated March 13, 2014
Start date January 2012
Est. completion date December 2013

Study information

Verified date March 2014
Source Center for Psychological Consultation
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The goal of this project is to improve access to effective treatments for obsessive compulsive disorder (OCD) through the use of web-based cognitive behavioral therapy (CBT) treatment. There intervention involves both a computer program (BT Steps) and human interaction via telephone. The investigators will test the efficacy and feasibility of computer therapy alone (n=35), computer plus a non-therapist coach (n=35), and computer plus a CBT therapist coach (n=35


Description:

The need for evidence-based mental health treatments i.e., 'treatment based on the best available science or research evidenceā€Ÿ1, has been stressed from scientific, ethical, and marketing perspectives. While empirical evidence supports both the efficacy and effectiveness of cognitive behavior therapy (CBT) for Obsessive-Compulsive Disorder (OCD), demand for clinicians trained in these approaches far exceeds supply. New technologies provide the opportunity to facilitate access to this specialized treatment. A growing body of research has found that web-based self-administered psychotherapy is highly effective, cost-efficient, and can achieve clinical improvements similar to those obtained with clinician administered therapy. The long-term goal of this project is to improve clinical and occupational functioning and decrease disability associated with OCD by improving access to effective treatments through the use of web-based CBT treatment. The intervention involves a computer program (BT STEPS) and human interaction via telephone. The inclusion of human interaction for coaching and encouragement has been found to significantly increase compliance and success rates in computerized self-help. Whether treatment outcomes differ when this coaching is done by a therapist versus when done by a trained non-therapist has not been studied. This is the first program to examine a hybrid model involving different levels of remote clinician coaching in combination with an on-line self-help tutorial. In Phase I the investigators will test the efficacy and feasibility of computer therapy alone (n=35), computer plus nontherapist coach (n=35) and computer plus CBT therapist coach. In phase II the investigators will do a fully powered study comparing our model to traditional face-to-face therapy.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age 18 or above

- Have clinically significant OCD

- YBOCS score of 16-32

Exclusion Criteria:

- Significant comorbid depression

- Serious suicide risk

- Psychosis or psychotic disorder

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Behavioral:
Computer-Assisted Cognitive Behavior Therapy (BT STEPS)
BT STEPS is a computer-assisted self help treatment for OCD. Clients work through the program at their own pace.

Locations

Country Name City State
United States Center for Psychological Consultation Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
Center for Psychological Consultation

Country where clinical trial is conducted

United States, 

References & Publications (1)

Greist JH, Marks IM, Baer L, Kobak KA, Wenzel KW, Hirsch MJ, Mantle JM, Clary CM. Behavior therapy for obsessive-compulsive disorder guided by a computer or by a clinician compared with relaxation as a control. J Clin Psychiatry. 2002 Feb;63(2):138-45. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Yale Brown Obsessive Compulsive Scale (YBOCS) YBOCS measures severity of obsessions and compulsions Change from Baseline on YBOCS at 12 weeks No
Secondary PHQ-9 PHQ-9 assesses the 9 core DSM symptoms of depression Change from baseline on PHQ9 at 12 weeks Yes
Secondary Work and Social Adjustment Scale (WSA) Measures problems at work and social relationships Change from baseline on WSA at 12 weeks No
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