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Completed

NCT Number: NCT00071578

Comparing Two Group Therapy Treatments for Binge Eating Disorder

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Stanford University Medical Center

Stanford, California, 94305-5722, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Group Psychotherapy-Negative Emotion Focus

Behavioral

20 weekly sessions, 2 hours, group format

Group Psychotherapy- Self-Esteem Focus

Behavioral

20 weekly sessions, 2 hours, group format

Primary outcomes

  1. frequency of binge eating

    Time frame: prior 4 weeks

Secondary outcomes

  1. Emotional Eating Scale

    Time frame: prior 7 days

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

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

Important dates

Study start
2003
Primary completion
2007
Study completion
2007
First posted
Oct 30, 2003
Registry last updated
Jun 27, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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