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Clinical Trials/NCT00158340
NCT00158340
Completed
Not Applicable

Binge Eating Self-Guided Treatment (BEST)

Kaiser Permanente2 sites in 1 country284 target enrollmentAugust 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Eating Disorders
Sponsor
Kaiser Permanente
Enrollment
284
Locations
2
Primary Endpoint
Frequency of binge eating
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

This study will determine the effectiveness of guided self-help treatment in treating individuals with binge eating disorder (BED).

Detailed Description

Binge eating disorder (BED) is a serious condition characterized by compulsive overeating and feelings of powerlessness. The condition often has a negative impact on both physical and emotional health. This study will examine ways to help people determine whether they have BED and will test whether guided self-help (GSH) treatment is effective in treating BED. Participants will be randomly assigned to receive either GSH treatment or usual clinical care (which may include general support and talk therapy) for 3 months. The GSH treatment is a cognitive behavioral therapy-based program that will be administered over 8 sessions. Participants receiving GSH will be given a book that focuses on dealing with BED; they will also meet with a therapist regularly to have their progress monitored. The Eating Disorders Examination (EDE), self-reports, questionnaires, and surveys will be used to assess participants. Assessments will be conducted at study entry, at Weeks 2 and 4 of the treatment, at the end of the treatment, and at 6 and 12 months post-treatment.

Registry
clinicaltrials.gov
Start Date
August 2004
End Date
July 2008
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of binge eating disorder (BED) bulimia nervosa (BN), or spectrum BN, defined as recurrent binge eating at least once a week for 3 months
  • Body mass index (BMI) between 18 and 45
  • Continuous membership in the Kaiser Permanente Northwest Division for at least 12 months prior to study entry

Exclusion Criteria

  • Diagnosis of anorexia nervosa or psychotic disorder
  • Significant organic brain syndromes, retardation, pervasive developmental disorder, or autism
  • At risk for suicide
  • Pregnancy

Outcomes

Primary Outcomes

Frequency of binge eating

Time Frame: Measured at post-treatment, Week 12, Month 6, and Year 1

Secondary Outcomes

  • Frequency of inappropriate compensatory behaviors, dietary restraint, over-valuation of weight/shape, functional impairment, self-esteem, and social impairment(Measured at post-treatment, Week 12, Month 6, and Year 1)
  • Body weight(Measured at post-treatmentand Year 1)

Study Sites (2)

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