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Clinical Trials/NCT00071578
NCT00071578
Completed
Not Applicable

Comparison of Dialectical Behavior Therapy and Supportive Therapy for Binge Eating Disorder

Stanford University1 site in 1 country101 target enrollmentOctober 2003

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Eating Disorders
Sponsor
Stanford University
Enrollment
101
Locations
1
Primary Endpoint
frequency of binge eating
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This study will compare two different approaches for the treatment for Binge Eating Disorder.

Detailed Description

Binge Eating Disorder (BED) is associated with impairments in physical, psychological, and social functioning. Research has revealed relationships between disordered eating and both low self-esteem and negative emotional states. Participants in this study will complete assessment interviews regarding their eating disorder and associated problems. Similar assessments will be conducted at the end of the study. Participants will then be randomly assigned to one of two therapy groups. Participants in one group will focus on the role of self-esteem, self-awareness, and personal effectiveness in binge eating. Participants in the other group will focus on the role of negative emotions and binge eating. Both treatments will involve a 30 to 40 minute pre-treatment individual orientation session, followed by 20 weeks of weekly group therapy. Sessions will take place over 22 weeks, or approximately 6 months (18 weekly sessions followed by 2 biweekly sessions). Follow-up assessments will take place at 3 months, 6 months, and 12 months after study completion to assess maintenance of treatment effects.

Registry
clinicaltrials.gov
Start Date
October 2003
End Date
July 2007
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Debra L. Safer

Asst professor

Stanford University

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of Binge Eating Disorder
  • Reside in the San Francisco Bay Area
  • Willing to commit to the study requirements

Exclusion Criteria

  • Unstable medical problems
  • History of bipolar illness or schizophrenia
  • Receiving treatment for an eating disorder (or unwillingness to discontinue treatment upon study entry)
  • Membership in weight-loss groups such as Weight Watchers or Jenny Craig (or unwillingness to discontinue membership upon study entry)
  • Use of medications affecting weight or appetite. Antidepressants are acceptable, but doses of any psychiatric medication must have been stable for at least 3 months prior to study start
  • Breast-feeding
  • Require gastric-bypass surgery

Outcomes

Primary Outcomes

frequency of binge eating

Time Frame: prior 4 weeks

Secondary Outcomes

  • Emotional Eating Scale(prior 7 days)

Study Sites (1)

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