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Clinical Trials/NCT01850433
NCT01850433
Completed
Not Applicable

Internet-based Cognitive Behavior Therapy for Body Dysmorphic Disorder: A Pilot Study

Karolinska Institutet1 site in 1 country23 target enrollmentMarch 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Body Dysmorhpic Disorder
Sponsor
Karolinska Institutet
Enrollment
23
Locations
1
Primary Endpoint
Body dysmorphic disorder symptoms
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The primary aim is to develop, and test the feasibility, of a novel and protocol-based cognitive behaviour therapy (CBT) treatment for body dysmorphic disorder (BDD) administered via the Internet.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
March 2014
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christian Rück

Associate professor, M.D.

Karolinska Institutet

Eligibility Criteria

Inclusion Criteria

  • outpatients
  • male or female
  • ≥ 18 years
  • currently living in Stockholm county
  • primary diagnosis of BDD according to the DSM-IV-TR
  • signed informed consent
  • regular access to a computer with Internet access and skills to use the web.

Exclusion Criteria

  • psychotropic medication changes within two months prior to the treatment
  • completed CBT for BDD within the last 12 months
  • BDD-YBOCS \< 12 at psychiatrist visit
  • other primary axis I diagnosis
  • current substance dependence
  • lifetime bipolar disorder or psychosis
  • suicidal ideation
  • Axis II diagnosis that could jeopardize treatment participation
  • other current psychological treatment that could affect BDD symptoms

Outcomes

Primary Outcomes

Body dysmorphic disorder symptoms

Time Frame: Measured after 12 weeks of treatment, and after 3 months after treatment

Secondary Outcomes

  • Depressive symptoms(After 12 weeks of treatment, and 3 months after treatment)
  • Functioning and life satisfaction(After 12 weeks of treatment, and 3 months after treatment)

Study Sites (1)

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