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Clinical Trials/NCT00934583
NCT00934583
Completed
Not Applicable

Preventing Eating Disorders and Reducing Comorbidity

Stanford University2 sites in 1 country549 target enrollmentAugust 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Eating Disorders
Sponsor
Stanford University
Enrollment
549
Locations
2
Primary Endpoint
Eating disorder diagnoses
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This study will examine the ability of an Internet-based program to prevent college-aged women from developing eating disorders.

Detailed Description

Approximately 2% to 4% of college-aged women suffer from eating disorders (EDs), and many more are at risk of developing them. A previous Internet-based intervention called Student Bodies (SB), which focused on body image concerns, was effective in reducing risk factors for EDs among college-aged women. However, the original SB program did not account for certain other risk factors, such as depression and compensatory behaviors like self-induced vomiting, over-exercising, or use of diuretics. Image and Mood (IaM) is an enhanced version of the SB program and takes into account depressive symptoms and the use of compensatory behaviors. This study will examine whether IaM will reduce ED risk factors in a large population of college women who are at high risk of developing EDs. Participation in this study will last 10 weeks. Participants will be randomly assigned to either receive the IaM program or be placed on a wait list. The IaM program, which will be delivered through the Internet, will provide information about nutrition, exercise, body image, and coping skills-including examples and exercises. It will also include an online message board monitored by a study psychologist. Each week the IaM participants will monitor their behavior, keep a journal about their experiences, and answer self-report questionnaires. Assessments of eating disorder symptoms; weight and shape concerns; depressive symptoms; and incidence of substance abuse, anxiety, or depressive disorders will be completed post-treatment and at 1- and 1.5-month follow-ups. Those assigned to the wait list will complete these assessments and then receive the IaM program after the last follow-up.

Registry
clinicaltrials.gov
Start Date
August 2009
End Date
April 2012
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Craig Barr Taylor

Professor

Stanford University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Eating disorder diagnoses

Time Frame: Measured after 10 weeks, 1 year, and 1.5 years

Secondary Outcomes

  • Weight Concerns Scale(Measured after 10 weeks, 1 year, and 1.5 years)
  • Eating Disorder Examination Questionnaires (EDE-Q)(Measured after 10 weeks, 1 year, and 1.5 years)
  • Depressive symptoms, as measured by the Beck Depression Inventory and Center for Epidemiologic Studies-Depression Scale(Measured after 10 weeks, 1 year, and 1.5 years)
  • Combined incidence of substance abuse, alcohol abuse, anxiety disorders, and depressive disorders(Measured after 10 weeks, 1 year, and 1.5 years)

Study Sites (2)

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