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Comparing Two Group Therapy Treatments for Binge Eating Disorder

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00071578
Enrollment
101
Registered
2003-10-30
Start date
2003-10-31
Completion date
2007-07-31
Last updated
2013-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eating Disorders

Keywords

Psychotherapy, Treatment

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.

Interventions

BEHAVIORALGroup Psychotherapy-Negative Emotion Focus

20 weekly sessions, 2 hours, group format

BEHAVIORALGroup Psychotherapy- Self-Esteem Focus

20 weekly sessions, 2 hours, group format

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
frequency of binge eatingprior 4 weeks

Secondary

MeasureTime frame
Emotional Eating Scaleprior 7 days

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026