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Reducing Eating Disorder Risk Factors - Article


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Binge Eating Disorder

BED 




Clinical Trial: Reducing Eating Disorder Risk Factors

This study is no longer 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 determine whether a web-based program is effective in reducing the incidence of eating disorders in college women who are at high risk for developing an eating disorder.

Condition Treatment or Intervention
Eating Disorders
 Behavior: Web-based intervention to reduce eating disorder risk factors

MedlinePlus related topics:  Eating Disorders

Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Placebo Control, Parallel Assignment, Efficacy Study

Official Title: Interventions to Reduce Eating Disorder Risk Factors

Further Study Details: 

Expected Total Enrollment:  660

Study start: February 2001

Female college students who use unhealthy weight control methods and have body image concerns may be at risk for developing an eating disorder. Developing and evaluating interventions to reduce eating disorders in high-risk populations is of great public health importance.

Participants are randomly assigned to either join a web-based risk-reduction program or receive no intervention. The 9-week risk-reduction program focuses on reducing body image and weight/shape concerns, identifying the risks of eating disorders, and increasing healthy weight regulation practices. The program includes weekly readings, writing assignments, and participation in a moderated electronic discussion group. Changes in body mass index (BMI) and the occurrence of major stressors and psychiatric events are assessed to determine their impact on the incidence of eating disorders. One-year incidence of eating disorders is determined by a diagnostic interview, and follow up may continue for up to 2.5 years.

Eligibility

Ages Eligible for Study:  18 Years   -   30 Years,  Genders Eligible for Study:  Female

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

  • College students at risk for developing an eating disorder

Exclusion Criteria:

  • Suicidal or other severe psychopathology
  • Alcohol or drug abuse
  • Body mass index (BMI) < 18 or > 32
  • Current diagnosis of anorexia nervosa, binge eating disorder, or bulimia nervosa and have been in treatment within the past 6 months

Location Information


California
      Stanford University, Dept. of Psychiatry and Behavioral Sciences, Stanford,  California,  94305,  United States

More Information

Study ID Numbers:  60453-01A1
Record last reviewed:  December 2004
Last Updated:  December 21, 2004
Record first received:  December 16, 2002
ClinicalTrials.gov Identifier:  NCT00050570
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 30, 2009



Page Updated: October 3, 2005
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