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Effectiveness of Binge Eating Disorder Treatments

Effectiveness of Psychological Treatments for BED

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00060762
Enrollment
205
Registered
2003-05-13
Start date
2002-04-30
Completion date
2007-03-31
Last updated
2014-05-15

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

Conditions

Eating Disorders

Keywords

Weight Loss

Brief summary

This study will evaluate the long-term effectiveness of interpersonal psychotherapy, behavioral weight loss interventions, and guided self help treatments in treating binge eating disorder (BED).

Detailed description

BED is a serious condition that is associated with psychiatric comorbidity, psychosocial impairment, and obesity. Interpersonal psychotherapy (IPT), behavioral weight loss (BWL) interventions, and guided self help (GSH) treatments for BED have been evaluated, but the safest and most effective treatment has not yet been identified. This study will determine which of these three treatments is most effective in treating BED. Participants are stratified by negative affect subtype and are randomly assigned for 6 months to one of three treatment groups: IPT, BWL, or GSH. IPT focuses on current interpersonal problems which are hypothesized to increase negative affect and lead to binge eating. BWL interventions involve the adoption of weight loss inducing behaviors. GSH is a shortened version of cognitive behavioral therapy that focuses directly on eating behavior. IPT and BWL patients have 20 treatment sessions; those receiving GSH have 10 sessions. Assessments are made pre-treatment, post-treatment, and at 6, 12, 18, and 24 months after treatment is complete.

Interventions

20 sessions of interpersonal therapy were provided over a 6-month period

20 sessions of behavioral weight loss treatment were provided over a 6-month period

10 sessions of guided self help were provided over a 6-month period

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 65 Years
Healthy volunteers
No

Inclusion criteria

* DSM-IV criteria for Binge Eating Disorder * Body Mass Index (BMI) between 27 and 45

Exclusion criteria

* Body Mass index \> 45 * Current psychosis * Current bipolar disorder * Alcohol or drug dependence within last 6-months

Design outcomes

Primary

MeasureTime frameDescription
Binge eatingPre-treatment, 6, 12, and 24-monthsRate of binge eating

Secondary

MeasureTime frameDescription
Eating disorder psychopathologypre-treatment, 6, 12, 24 monthsAssessed by the Eating Disorder Examination

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026