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CompletedNCT01126918Updated Sep 30, 2016

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

An interventional study of Body Project in Eating Disorders and Obesity, sponsored by Oregon Research Institute. Completed at 7 sites in United States. Open to female participants, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-09-30.

Sponsored by Oregon Research Institute · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
432
Allocation
Randomized
Sex
Female
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Study 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.

Read the 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.

02

Conditions studied

  • Eating Disorders
  • Obesity

Keywords

  • Eating Disorders
  • Obesity
  • Body Dissatisfaction
  • Female
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In context

Feeding and Eating Disorders

740 studies on the registry are indexed under Feeding and Eating Disorders; 159 are open to participants now.

This study's enrollment of 432 is above the median of 75 across 540 interventional studies indexed under Feeding and Eating Disorders.

Browse Feeding and Eating Disorders studies →

Lead sponsor

Oregon Research Institute is the lead sponsor of 70 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • meets DSM-IV criteria for anorexia nervosa, bulimia nervosa, or binge eating disorder
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
432 participants (actual)

Study arms

  • Active comparator
    Brochure Condition

    Participants in this condition receive an educational brochure about healthy body image via post-mail.

    Behavioral: Body Project

  • Experimental
    Group Condition

    Participants in this condition 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.

    Behavioral: Body Project

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.

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What researchers measure

Primary outcomes

  1. eating disorder symptoms, risk for future eating disorder and obesity onset

    Time frame: 2 years

Secondary outcomes

  1. mediators to intervention effects

    We will test whether the dissonance program intervention effects are mediated by change in thin-ideal internalization

    Time frame: 2 years

  2. moderators to program effects

    We will test whether certain factors moderate program effects (e.g., initial body dissatisfaction level).

    Time frame: 2 years

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Study locations

7 sites
  • Northwest Christian University
    Eugene, Oregon 97401, United States
  • University of Oregon
    Eugene, Oregon 97403, United States
  • Drexel University
    Philadelphia, Pennsylvania 19104, United States
  • University of Pennsylvania
    Philadelphia, Pennsylvania 19104, United States
  • Temple University
    Philadelphia, Pennsylvania 19122, United States
  • University of Texas at Austin
    Austin, Texas 78712, United States
  • Southwestern University
    Georgetown, Texas 78626, United States
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References and documents

Publications

  • Stice E, Desjardins CD, Rohde P. Young women who develop anorexia nervosa exhibit a persistently low premorbid body weight on average: A longitudinal investigation of an important etiologic clue. J Psychopathol Clin Sci. 2022 Jul;131(5):479-492. doi: 10.1037/abn0000762. Epub 2022 Jun 2. PubMed 35653756 ↗
  • Stice E, Desjardins CD, Rohde P, Shaw H. Sequencing of symptom emergence in anorexia nervosa, bulimia nervosa, binge eating disorder, and purging disorder and relations of prodromal symptoms to future onset of these disorders. J Abnorm Psychol. 2021 May;130(4):377-387. doi: 10.1037/abn0000666. PubMed 34180702 ↗
  • Stice E, Rohde P, Shaw H, Desjardins C. Weight suppression increases odds for future onset of anorexia nervosa, bulimia nervosa, and purging disorder, but not binge eating disorder. Am J Clin Nutr. 2020 Oct 1;112(4):941-947. doi: 10.1093/ajcn/nqaa146. PubMed 32534455 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 30, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01126918
Lead sponsor
Oregon Research Institute
Collaborators
University of Texas at Austin, Drexel University
Responsible party
Sponsor
First posted
May 20, 2010
Start date
Apr 2010
Primary completion
Dec 2015
Completion
Feb 2016
Last update
Sep 30, 2016

Study contacts

Eric Stice, Ph.D.
principal investigator · Oregon Research Institute
Meghan Butryn, Ph.D.
principal investigator · Drexel University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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