The Peer-Delivered Body Project for Young Women in High School

Sponsor
University of Colorado, Boulder (Other)
Overall Status
Completed
CT.gov ID
NCT04263155
Collaborator
(none)
74
1
2
19.9
3.7

Study Details

Study Description

Brief Summary

This study will evaluate the impact of the Body Project (a dissonance-based program designed to address body image concerns and prevent eating disorders) on key eating disorder risk factors and relevant social and self-constructs at three time-points (pre, post, and one-year follow-up). Young women will be recruited from two high schools and will be randomized to receive the Body Project or to the control group. The Body Project will be facilitated by college-aged women.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: The Body Project
N/A

Detailed Description

Preventive models that can avert the onset of eating disorders and innovative delivery methods that increase engagement with care offer a promising approach to improving the mental health and wellness of young women. This study aims to implement and evaluate the Body Project, a 4-hour dissonance-based program designed to address body image concerns and prevent eating disorders with high school young women using a peer delivery model. This study will evaluate the impact of the Body Project on key eating disorder risk factors and relevant social and self-constructs at three time-points (pre, post, and one-year follow-up). Young women will be recruited from two high schools and will be randomized to receive the Body Project program or to the control group. The Body Project will be facilitated by college-aged young women who have been trained to deliver the Body Project.

Study Design

Study Type:
Interventional
Actual Enrollment :
74 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Implementation and Evaluation of the Peer-Delivered Body Project for Young Women in High School
Actual Study Start Date :
Aug 1, 2018
Actual Primary Completion Date :
Mar 30, 2020
Actual Study Completion Date :
Mar 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental: The Body Project for high school young women

The 4-hour Body Project workshop delivered by trained peer leaders

Behavioral: The Body Project
The Body Project is a 4-hour dissonance-based program designed to address body image concerns and prevent eating disorders. The curriculum consists of written, verbal, and behavioral exercises that provide participants with the opportunity to voluntarily and publicly critique the appearance ideal.

No Intervention: Control

The business-as-usual comparison group does not participate in the Body Project but may engage in any other programs or services they normally would

Outcome Measures

Primary Outcome Measures

  1. Change in Thin-Ideal Internalization Scale [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of endorsement of the thin ideal (scale 1-5 with higher scores indicating higher levels of thin ideal internalization)

  2. Change in Satisfaction and Dissatisfaction with Body Parts Scale [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of body dissatisfaction (scale 1-5 with higher scores indicating higher levels of dissatisfaction)

  3. Change in Dutch Restrained Eating Scale [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of dietary restraint (scale 1-5 with higher scores indicating higher levels of eating restraint)

  4. Change in Positive Affect and Negative Affect Scale-Revised [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of negative affect (scale 1-5 with higher scores indicating higher levels of negative affect)

Secondary Outcome Measures

  1. Change in Objectified Body Consciousness Scale - Body Surveillance Subscale [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of body monitoring and surveillance (scale 1-7 with higher scores indicating higher levels of body surveillance)

  2. Change in UCLA Loneliness Scale [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of loneliness (scale 1-4 with higher scores indicating higher levels of loneliness)

  3. Change in Inventory of Peer Influence on Eating Concerns [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of peer influence on eating and body concerns (scale 1-5 with higher scores indicating higher levels of peer influence)

  4. Change in Patient Health Questionnaire (PHQ-9) [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure for depressive symptom severity(scale 0-3 with higher scores indicating higher levels of depression)

  5. Change in Generalized Anxiety Disorder (GAD-7) [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure for symptoms of generalized anxiety (scale 0-3 with higher scores indicating higher levels of anxiety)

  6. Change in General Self-Efficacy Scale [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of self-efficacy (scale 1-4 with higher scores indicating higher levels of self-efficacy)

  7. Change in Self-Compassion Scale [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of self-compassion (scale 1-5 with higher scores indicating higher levels of self-compassion)

  8. Change in Rosenberg Self-Esteem Scale [Baseline, Post-intervention (4 weeks after baseline), 1 year post-intervention follow-up]

    Self-report measure of global self-worth (scale 1-4 with higher scores indicating higher levels of self-esteem)

  9. Sense of Belonging (Body Project group only) [Baseline]

    Self-report measure of anticipated belonging with group (scale 1-7 with higher scores indicating higher levels of anticipated belonging)

  10. Sense of Belonging Follow-Up (Body Project group only) [Post-intervention (4 weeks after baseline)]

    Self-report measure of belonging with group (scale 1-7 with higher scores indicating higher levels of experienced belonging)

  11. Working Alliance Inventory (Body Project group only) [Post-intervention (4 weeks after baseline)]

    Self-report measure of therapeutic alliance with peer leaders (scale 1-5 with higher scores indicating higher levels of working alliance)

  12. Program Satisfaction (Body Project group only) [Post-intervention (4 weeks after baseline)]

    Self-reported ratings of satisfaction with program and peer leaders (scale 1-4 with higher scores indicating higher levels of program satisfaction)

  13. Fidelity and Competence (Body Project group only) [From the first Body Project session to the final (fourth) Body Project session, 4 weeks on average]

    Observer-rated assessments of peer leader fidelity and competence (scale 1-10 with higher scores indicating higher levels of facilitator fidelity and competence)

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Female high school student
Exclusion Criteria:
  • Previous participation in the Body Project program

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Colorado Boulder Boulder Colorado United States 80309

Sponsors and Collaborators

  • University of Colorado, Boulder

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sona Dimidjian, Principal Investigator, University of Colorado, Boulder
ClinicalTrials.gov Identifier:
NCT04263155
Other Study ID Numbers:
  • 18-0007-01
First Posted:
Feb 10, 2020
Last Update Posted:
Jun 26, 2020
Last Verified:
Jun 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sona Dimidjian, Principal Investigator, University of Colorado, Boulder
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 26, 2020