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Completed

NCT Number: NCT00158340

Guided Self-Help Treatment for Binge Eating Disorder

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

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Wesleyan University Department of Psychology, Middletown, Connecticut, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Guided self-help cognitive behavioral therapy (CBT)

Behavioral

Participants receive eight sessions of guided self-help CBT.

Usual clinical care

Behavioral

Control group participants receive treatment as usual.

Primary outcomes

  1. Frequency of binge eating

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

Secondary outcomes

  1. Frequency of inappropriate compensatory behaviors, dietary restraint, over-valuation of weight/shape, functional impairment, self-esteem, and social impairment

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

  2. Body weight

    Time frame: Measured at post-treatmentand Year 1

Sponsors and collaborators

Lead sponsor

Kaiser Permanente

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Binge Eating Self-Guided Treatment (BEST)

Acronym: BEST

Important dates

Study start
2004
Primary completion
2008
Study completion
2008
First posted
Sep 12, 2005
Registry last updated
Nov 7, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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