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Effectiveness of Binge Eating Disorder Treatments - Article


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Eating Disorders

Anorexia; Binge Eating; Bulimia; Eating Disorder 




Clinical Trial: Effectiveness of Binge Eating Disorder Treatments

This study is currently recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

Purpose

The purpose of this study is to evaluate the long-term effectiveness of three Binge Eating Disorder (BED) treatments.

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

MedlinePlus related topics:  Eating Disorders

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: 

Expected Total Enrollment:  210

Study start: April 2002;  Expected completion: March 2005

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   -   65 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

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

Location and Contact Information


California
      W. Stewart Agras, Stanford,  California,  94305,  United States; Recruiting
W. S. Agras, MD  650-723-7107    sagras@stanford.edu 
Stewart Agras, MD,  Principal Investigator

Missouri
      Washington University School of Medicine, St. Louis,  Missouri,  United States; Recruiting
Sean Monaghan  314-286-0070 
Denise E. Wilfley, PhD,  Principal Investigator

More Information

Study ID Numbers:  63863-01A1
Record last reviewed:  August 2004
Last Updated:  October 13, 2004
Record first received:  May 12, 2003
ClinicalTrials.gov Identifier:  NCT00060762
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

Resources



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November 29, 2009



Page Updated: October 15, 2009
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