NCT00184262

Brief Summary

The aim of the study is to determine whether exposure and response prevention (ERP) is more effective when patients are presented with a behavioral therapy versus cognitive therapy rationale in the treatment of obsessive-compulsive disorder (OCD).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
35

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2003

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2003

Completed
2.7 years until next milestone

First Submitted

Initial submission to the registry

September 13, 2005

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 16, 2005

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2006

Completed
Last Updated

March 21, 2012

Status Verified

March 1, 2012

First QC Date

September 13, 2005

Last Update Submit

March 20, 2012

Conditions

Outcome Measures

Primary Outcomes (1)

  • scores on Y-BOCS and SCID-I

    3 months

Study Arms (2)

ERP cognitive therapy

ACTIVE COMPARATOR
Behavioral: ERP cognitive therapy

ERP behavioral therapy

EXPERIMENTAL
Behavioral: ERP behavioral therapy

Interventions

15 exposure and response prevention (ERP) sessions in 3 months with a cognitive therapy rationale

Also known as: exposure and response prevention + cognitive therapy
ERP cognitive therapy

15 exposure and response prevention (ERP) sessions in 3 months with a behavioral therapy rationale

Also known as: exposure and response prevention + behavioral therapy
ERP behavioral therapy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Obsessive-compulsive disorder

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Norwegian University of Science and Technology, INM

Trondheim, 7441, Norway

Location

Related Publications (1)

  • Hansen B, Vogel PA, Stiles TC, Gotestam KG. Influence of co-morbid generalized anxiety disorder, panic disorder and personality disorders on the outcome of cognitive behavioural treatment of obsessive-compulsive disorder. Cogn Behav Ther. 2007;36(3):145-55. doi: 10.1080/16506070701259374.

MeSH Terms

Conditions

Obsessive-Compulsive Disorder

Interventions

Cognitive Behavioral TherapyBehavior Therapy

Condition Hierarchy (Ancestors)

Anxiety DisordersMental Disorders

Intervention Hierarchy (Ancestors)

PsychotherapyBehavioral Disciplines and Activities

Study Officials

  • K. Gunnar Götestam, PhD MD

    Norwegian University of Science and Technology

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 13, 2005

First Posted

September 16, 2005

Study Start

January 1, 2003

Study Completion

December 1, 2006

Last Updated

March 21, 2012

Record last verified: 2012-03

Locations