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Effectiveness of Binge Eating Disorder Treatments

This study has been completed.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00060762
  Purpose

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).


Condition Intervention Phase
Eating Disorders
Behavioral: Interpersonal Therapy
Behavioral: Behavioral Weight Loss Treatment
Behavioral: Guided Self Help
Phase IV

MedlinePlus related topics:   Eating Disorders    Weight Control   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title:   Effectiveness of Psychological Treatments for BED

Further study details as provided by National Institute of Mental Health (NIMH):

Estimated Enrollment:   210
Study Start Date:   April 2002
Estimated Study Completion Date:   March 2005

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.

  Eligibility
Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

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

Please refer to this study by its ClinicalTrials.gov identifier: NCT00060762

Locations
United States, California
W. Stewart Agras    
      Stanford, California, United States, 94305
United States, Missouri
Washington University School of Medicine    
      St. Louis, Missouri, United States, 63100
United States, New Jersey
Rutgers University Eating Disorder Clinic    
      Piscataway, New Jersey, United States, 08854

Sponsors and Collaborators
  More Information


Responsible Party:   Stanford University ( W. Stewart Agras )
Study ID Numbers:   R01 MH63863, DSIR 83-ATAS
First Received:   May 12, 2003
Last Updated:   November 7, 2008
ClinicalTrials.gov Identifier:   NCT00060762
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
Weight Loss  

Study placed in the following topic categories:
Body Weight
Bulimia Nervosa
Mental Disorders
Bulimia
Weight Loss
Eating Disorders

Additional relevant MeSH terms:
Pathologic Processes
Disease

ClinicalTrials.gov processed this record on November 30, 2008




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