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Binge Eating Disorder:Guided Self-Help Treatment for Binge Eating Disorder
By Clinical Trials
Sep 30, 2006, 12:12
Guided Self-Help Treatment for Binge Eating Disorder
This study is currently recruiting patients.
Verified by National Institute of Mental Health (NIMH) September 2006
Purpose
This study will determine the effectiveness of guided self-help (GSH) treatment in treating individuals with binge eating disorder (BED).
| Condition |
Intervention |
Eating Disorders Hyperphagia Bulimia
|
Behavior: Guided self-help Behavior: Usual clinical care
|
MedlinePlus related topics: Eating Disorders
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Binge Eating Self-Guided Treatment (BEST)
Further study details as provided by National Institute of Mental Health (NIMH):
Primary Outcomes: Frequency of binge eating at baseline, Week 12, Month 6, and Month 12
Secondary Outcomes: Frequency of inappropriate compensatory behaviors, dietary restraint, overevaluation of weight/shape, functional impairment, self-esteem, and social impairment assessed at baseline, 12 weeks, 6 months, and 12 months; body weight assessed at baseline and 12 months
Expected Total Enrollment: 200
Study start: August 2004; Expected completion: July 2009
Last follow-up: July 2008; Data entry closure: July 2008
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 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.
Eligibility
Ages Eligible for Study: 18 Years - 50 Years, Genders Eligible for Study: Both
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
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00158340
Connecticut Wesleyan University Department of Psychology, Middletown, Connecticut, 06459, United States; Recruiting
Oregon Kaiser Permanente Center for Health Research, Portland, Oregon, 97227, United States; Recruiting
Study chairs or principal investigators
Ruth H. Striegel-Moore, PhD, Principal Investigator, Wesleyan University
More Information
Study ID Numbers: R01 MH66966; DSIR 83-ATAS
Last Updated: September 22, 2006
Record first received: September 7, 2005
ClinicalTrials.gov Identifier:
NCT00158340Health Authority: United States: Federal Government
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