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Eating Disorders Prevention: An Effectiveness Trial for At-Risk College Students

Eating Disorders Prevention: An Effectiveness Trial for At-Risk College Students

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01126918
Enrollment
432
Registered
2010-05-20
Start date
2010-04-30
Completion date
2016-02-29
Last updated
2016-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eating Disorders, Obesity

Keywords

Eating Disorders, Obesity, Body Dissatisfaction, Female

Brief summary

This three-site effectiveness trial will test whether a brief dissonance-based eating disorder prevention program produces intervention effects when college counselors, psychologists, and nurses are responsible for participant recruitment, screening, and intervention delivery under ecologically valid conditions.

Detailed description

Threshold and subthreshold eating disorders affect over 10% of young women and are associated with functional impairment, distress, psychiatric comorbidity, medical complications, mortality, and risk for obesity onset. Accordingly, a pressing public healthy priority is to develop effective prevention programs for eating pathology. The proposed project will be the first effectiveness trial to test whether an eating disorder prevention program with strong empirical support from efficacy trials produces effects under ecologically valid conditions among high-risk female college students, which is a vital step toward widespread dissemination of programs developed with NIH funding. The proposed cost-effectiveness analyses and examination of process factors that predict larger intervention effects will also represent novel contributions to the literature.

Interventions

BEHAVIORALBody Project

Participants in this intervention attend four 1-hour group meetings (one per week for four consecutive weeks) in which they complete a series of written and verbal exercises intended to increase body satisfaction.

Sponsors

University of Texas at Austin
CollaboratorOTHER
Drexel University
CollaboratorOTHER
Oregon Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* (1) is a registered student at a participating school, (2) self-reports body image concerns

Exclusion criteria

* meets DSM-IV criteria for anorexia nervosa, bulimia nervosa, or binge eating disorder

Design outcomes

Primary

MeasureTime frame
eating disorder symptoms, risk for future eating disorder and obesity onset2 years

Secondary

MeasureTime frameDescription
mediators to intervention effects2 yearsWe will test whether the dissonance program intervention effects are mediated by change in thin-ideal internalization
moderators to program effects2 yearsWe will test whether certain factors moderate program effects (e.g., initial body dissatisfaction level).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026