The Peer-Delivered "Mind. Body. Voice." Program for High School Women (Mbv) - Remote

May 15, 2023 updated by: Sona Dimidjian, University of Colorado, Boulder

Randomized Controlled Trial of the Peer-Delivered "Mind. Body. Voice." Eating Disorder Prevention Program Among High School Women - Remote

This study will evaluate the impact of a program (called mind. body. voice. or "mbv") that was collaboratively designed by youth, educators, and researchers, informed by the Body Project (Becker et al., 2013; Stice et al., 2019), Youth Participatory Action Research, an extended co-design process, and previous iterations of the mbv program. The study evaluates the impact of the mbv program on key aspects of mental health and well-being; specifically, body image and disordered eating symptoms, identity and agency, social and self-constructs, physical health and mood at three time points over the course of the 10-week program, which will be offered remotely in response to the COVID-19 pandemic. Students will be recruited from high schools and will be randomized to receive the mbv program or an assessment-only control group.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Eating disorders have the highest mortality rate of any psychiatric condition and are the second leading cause of mental health disability among young women. Given that eating disorders have their peak onset during adolescence (ages 16-19), prevention efforts among adolescent women are critical in order to avert the onset of these chronic and disabling disorders. The mbv program targets body image and appearance related pressures, awareness of body sensations, and agency and community building skills. The program consists of 10 weekly sessions and is delivered by peer facilitators. This study will implement and evaluate the mbv program at the high school level in order to examine the extent to which the program influences young women's mental health and well-being, particularly related to eating disorder risk factors and symptoms.

Utilizing a randomized controlled trial, the study seeks to address the following aims:

  1. To examine the impact of the mbv program on key aspects of mental health and well-being; specifically, body image and disordered eating symptoms, identity and agency, social and self- constructs, physical health and mood among participating high school women.
  2. To explore young women's experiences of participating in the program, including strengths and limitations and perspectives on specific activities.

Study Type

Interventional

Enrollment (Actual)

170

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Colorado
      • Boulder, Colorado, United States, 80309
        • University of Colorado Boulder

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • High school women, grades 9-12

Exclusion Criteria:

  • Prior participation in the Body Project or mind. body. voice. RCT

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Assessment-only control
Experimental: mind. body. voice.
The 10-week mind. body. voice. program.
The mbv program consists of 10 weekly sessions that include a variety of practices, including: cognitive dissonance exercises, contemplative practices, guided discussion and community building.
Other Names:
  • Healthy Body, Mind, and Voice

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Body Appreciation Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of body appreciation (scale 1-5 with higher scores indicating higher levels of appreciation)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Engaged Living Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of values-based living (scale 1-5 with higher scores indicating higher levels of living based on values)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Multidimensional Assessment of Interoceptive Awareness
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of somatic awareness (scale 1-5 with higher scores indicating higher levels of somatic awareness)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Social Contribution Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of sense of contributing to society (scale 1-5 with higher scores indicating higher levels of contribution)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Sociocultural Pressures Around Appearance
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of sociocultural pressures related to appearance (scale 1-5 with higher scores indicating higher levels of pressure)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Internalization of Media Appearance Ideals
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of internalized appearance ideals in the media (scale 1-5 with higher scores indicating higher levels of internalization)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Ideal Body Stereotype Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of internalization of ideal body stereotypes (scale 1-5 with higher scores indicating higher levels of internalization)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Self-Compassion Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of compassion for oneself (scale 1-5 with higher scores indicating higher levels of self-compassion)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Group Belonging Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of sense of anticipated (baseline) and experienced (follow-up) belonging with intervention program group (scale 1-7 with higher scores indicating higher levels of belonging)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Peer Influence on Appearance Concerns
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of influence of peers on appearance concerns (scale 1-5 with higher scores indicating higher levels of peer influence)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Dieting Behavior and Restraint
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of dieting behavior and restricted eating (scale 1-5 with higher scores indicating higher levels of dieting and restriction)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Body Dissatisfaction Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of body dissatisfaction (scale 1-5 with higher scores indicating higher levels of dissatisfaction
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Objectified Body Consciousness Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of body monitoring and surveillance (scale 1-5 with higher scores indicating higher levels of body surveillance)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Self-Liking Scale/Self-Competence Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of how much one likes oneself and considers oneself competent (scale 1-5 with higher scores indicating higher levels of self-liking and self-competence
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Self-Efficacy Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of effectiveness in handling challenges and achieving goals (scale 1-5 with higher scores indicating higher levels of self-efficacy)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Belonging Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of general sense of belonging (scale 1-5 with higher scores indicating higher levels of belonging)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Proactive Coping Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of ability to succeed (scale 1-5 with higher scores indicating higher levels of proactive coping)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Eating Attitudes Test 26
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of disordered eating behaviors (scale 1-6 with higher scores indicating higher levels of disordered eating)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in School Engagement and Belonging
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of engagement with schoolwork and belonging in school (scale 1-5 with higher scores indicating higher levels of engagement and belonging)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in School Grades and Attendance
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of grades and attendance
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Physical Health Questionnaire
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of health outcomes such as sleep and physical symptoms (scale 1-7 with higher scores indicating higher levels of health symptoms)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Positive and Negative Affect Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of positive and negative affect (scale 1-6 with higher scores indicating higher affect levels)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Patient Health Questionnaire A
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of depression (scale 1-4 with higher scores indicating higher levels of depression)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in UCLA Loneliness Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of loneliness (scale 1-4 with higher scores indicating higher levels of loneliness)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Humanitarian Egalitarian Scale
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of agreement with humanitarian and egalitarian values (scale 1-5 with higher scores indicating higher levels of agreement)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in Generalized Anxiety Disorder 7
Time Frame: Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Self-report measure of anxiety (scale 1-4 with higher scores indicating higher levels of anxiety)
Baseline, midway (5 weeks after baseline), post-intervention (10 weeks after baseline)
Change in COVID-19 impact
Time Frame: Baseline, midway, post-intervention (10 weeks after baseline)
Self-report measure of COVID-19 negative and positive life impact
Baseline, midway, post-intervention (10 weeks after baseline)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 9, 2020

Primary Completion (Actual)

May 31, 2022

Study Completion (Actual)

May 31, 2022

Study Registration Dates

First Submitted

October 10, 2020

First Submitted That Met QC Criteria

October 10, 2020

First Posted (Actual)

October 19, 2020

Study Record Updates

Last Update Posted (Actual)

May 17, 2023

Last Update Submitted That Met QC Criteria

May 15, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 18-0007-03

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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