Skip to main content
Clinical Trials/NCT02635152
NCT02635152
Completed
Not Applicable

Evaluation of an Internet-Based Treatment for Body Dysmorphic Disorder

Florida State University1 site in 1 country50 target enrollmentSeptember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Body Dysmorphic Disorder
Sponsor
Florida State University
Enrollment
50
Locations
1
Primary Endpoint
Yale-Brown Obsessive Compulsive Scale Modified for Body Dysmorphic Disorder (BDD-YBOCS; Phillips et al., 1997)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to determine whether a computerized intervention designed to reduce appearance and evaluation related interpretation biases will reduce symptoms associated with body dysmorphic disorder.

Detailed Description

The present study aims to examine the feasibility of a remote treatment for body dysmorphic disorder delivered via the Internet. To evaluate the efficacy of the IBM protocol we have developed in reducing negative appearance and evaluative related interpretations, we will conduct a two-arm randomized controlled trial over the internet. Individuals with a diagnosis of body dysmorphic disorder (N = 40) will be randomized to one of two conditions: 1) IBM or 2) progressive muscle relaxation. Each condition will consist of eight 10-25 minute treatment sessions. Participants will complete two sessions per week for four weeks and will be administered assessments at pre-treatment, one week post-treatment and at 3-month follow-up. We hypothesize that: 1) IBM will lead to greater reductions in BDD symptoms than the PMR condition; 2) IBM will lead to greater reductions in depression, anxiety and suicidal ideation than the PMR condition; 3) IBM will lead to greater reductions in threat interpretations and greater increases in benign interpretations than the PMR condition; 4) The effects of condition on BDD symptoms will be mediated by changes in BDD-related interpretation bias; and 5) The effects of training in the IBM condition will be maintained at the 3-month follow-up assessments.

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
March 2018
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jesse Cougle

Associate Professor

Florida State University

Eligibility Criteria

Inclusion Criteria

  • Current diagnosis of Body Dysmorphic Disorder according to DSM-5 criteria
  • BDD-YBOCS score greater than or equal to 20
  • Fluent in English
  • No significant physical defect or flaw in appearance (e.g., disfiguration)

Exclusion Criteria

  • History of psychotic disorder, bipolar disorder, borderline personality disorder
  • Current substance use disorder
  • Unstable medication status (i.e. change in medication within the last month)
  • Concurrent psychotherapy for appearance concerns
  • Active and clinically significant suicidality

Outcomes

Primary Outcomes

Yale-Brown Obsessive Compulsive Scale Modified for Body Dysmorphic Disorder (BDD-YBOCS; Phillips et al., 1997)

Time Frame: change from baseline at one-week post treatment and 3-months post-treatment

Measures past-week BDD symptom severity

Secondary Outcomes

  • Depressive Symptom Index-Suicidality Subscale(change from baseline at one-week post treatment and 3-months post-treatment)
  • Beck Anxiety Inventory (BAI; Steer & Beck, 1997)(change from baseline at one-week post treatment and 3-months post-treatment)
  • Beck Depression Inventory (BDI-II; Beck, Steer, & Brown, 1996)(change from baseline at one-week post treatment and 3-months post-treatment)
  • Body Dysmorphic Disorder Word Sentence Association Paradigm (BDD-WSAP; modified from Hindash & Amir, 2011)(change from baseline at one-week post treatment and 3-months post-treatment)

Study Sites (1)

Loading locations...

Similar Trials