Comparing Two Group Therapy Treatments for Binge Eating Disorder

Stanford University

Status: Completed

Conditions: Eating Disorders

Treatments: Behavioral: Group Psychotherapy-Negative Emotion Focus; Behavioral: Group Psychotherapy- Self-Esteem Focus

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00071578

K23MH066330 (U.S. NIH Grant/Contract)

DSIR 8K-RTAT

Details and patient eligibility

About

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

Full 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.

Enrollment: 101 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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101 participants in 2 patient groups, including a placebo group

1

Experimental group

Description:

Group therapy Negative Emotion Focus

Treatment:

Behavioral: Group Psychotherapy-Negative Emotion Focus

2

Placebo Comparator group

Description:

Group Psychotherapy- Self Esteem Focus

Treatment:

Behavioral: Group Psychotherapy- Self-Esteem Focus