- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07678554
Overvaluation of Weight and Shape Intervention vs The Body Project
Pilot Testing Overvaluation of Weight and Shape Intervention vs The Body Project
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Jasmine Lopez, BA
- Phone Number: 760-905-1706
- Email: jasglo@stanford.edu
Study Contact Backup
- Name: Nicole E Dunkel, BA
- Phone Number: 281-704-5033
- Email: ndunkel@stanford.edu
Study Locations
-
-
California
-
Stanford, California, United States, 94305
- Stanford University
-
Contact:
- Eric Stice, PhD
- Phone Number: 5412220615
- Email: estice@stanford.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Female-identifying
- High School
- College Adolescents
- Ages 14-22
Exclusion Criteria:
- Non-female identifying
- Outside of the United States
Study Plan
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 |
|---|---|
|
Experimental: Priorities
Arm: Participants randomly assigned to receieve the priorities intervention Priorities aims to reduce body image concerns, prevent eating disorders, bolster self-esteem, and promote mental and emotional health by helping participants identify and nurture alternative sources of self-worth. Priorities would use group discussions, role-plays & behavioral challenges, homework assignments & letter-writing, and self-worth activism to achieve this. Priorities script: https://shorturl.at/UzWQG |
Priorities aims to reduce body image concerns, prevent eating disorders, bolster self-esteem, and promote mental and emotional health by helping participants identify and nurture alternative sources of self-worth. Priorities would use group discussions, role-plays & behavioral challenges, homework assignments & letter-writing, and self-worth activism to achieve this. Priorities script: https://shorturl.at/UzWQG |
|
Active Comparator: Body Project
The Body Project is the only ED prevention program that has repeatedly reduced future onset of EDs, produced effects when evaluated by independent researchers, produced stronger effects than credible alternative interventions, and affected objective outcomes (Stice et al., 2019). The Body Project is a dissonance-based ED prevention program wherein high-risk young women with body image concerns collectively critique pursuit of the thin appearance ideal in verbal, written, and behavioral exercises. It has produced greater reductions in risk factors (pursuit of the thin ideal, body dissatisfaction, dieting, negative affect), ED symptoms, and future ED onset over a 2- to 4-year follow-ups than assessment-only control conditions and alternative interventions in over 25 controlled trials (e.g., Becker et al., 2010; Ghaderi et al.,2020; Halliwell & Diedrichs, 2014; Stice et al., 2000, 2006, 2008, 2011, 2013, 2017, 2020). Link to script: https://shorturl.at/6SSmP |
The Body Project is the only ED prevention program that has repeatedly reduced future onset of EDs, produced effects when evaluated by independent researchers, produced stronger effects than credible alternative interventions, and affected objective outcomes (Stice et al., 2019). The Body Project is a dissonance-based ED prevention program wherein high-risk young women with body image concerns collectively critique pursuit of the thin appearance ideal in verbal, written, and behavioral exercises. It has produced greater reductions in risk factors (pursuit of the thin ideal, body dissatisfaction, dieting, negative affect), ED symptoms, and future ED onset over a 2- to 4-year follow-ups than assessment-only control conditions and alternative interventions in over 25 controlled trials (e.g., Becker et al., 2010; Ghaderi et al.,2020; Halliwell & Diedrichs, 2014; Stice et al., 2000, 2006, 2008, 2011, 2013, 2017, 2020). Body Project Script: https://shorturl.at/6SSmP |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Priorities Questionnaire- updated
Time Frame: Both Priorities and the Body Project consist of four 1-hour weekly sessions occurring over four weeks. The questionnaire will be administered at baseline (before session 1), post-test (after session 4), 1 month follow up, and 3 month follow up.
|
Participants will be surveyed on the following measures before and after the intervention: self-report measure of weight/shape overvaluation, thin-ideal internalization, body dissatisfaction, harms from social media scale and mental health scales, depression questionnaire, anxiety questionnaire, PANAS scale for negative affect, as well as the self-report Eating Disorder Diagnostic Screen (assessing eating disorder symptoms using the Eating Disorder Diagnostic Survey (EDDS), a brief self-report scale.
The EDDS symptom composite contains convergent validity with the Eating Disorder Diagnostic Interview (EDDI) as well as closely aligned diagnosis).
|
Both Priorities and the Body Project consist of four 1-hour weekly sessions occurring over four weeks. The questionnaire will be administered at baseline (before session 1), post-test (after session 4), 1 month follow up, and 3 month follow up.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Eric Stice, PhD, Stanford University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Mental Disorders
- Signs and Symptoms, Digestive
- Somatoform Disorders
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Feeding and Eating Disorders
- Body Dysmorphic Disorders
- Delivery of Health Care
- Health Care Quality, Access, and Evaluation
- Health Care Economics and Organizations
- Health Planning
- Health Priorities
Other Study ID Numbers
- 79760
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Body Image
-
University of SheffieldCompletedBody Image Disturbance | Body Image | ShameUnited Kingdom
-
Chapman UniversityOhio State UniversityWithdrawn
-
Trakya UniversityMedipol UniversityCompleted
-
Duke UniversityTerminatedImage, BodyUnited States
-
University of the West of EnglandUnilever R&D; UNICEF; Deakin University; Talk 2 U; Instituto Federal Sudeste de Minas...Completed
-
University of the West of EnglandTata Institute of Social Sciences; Lady Shri Ram College for WomenCompleted
-
University of the West of EnglandC&R Research, Inc.; Unilever R&DRecruitingBody ImageUnited States
-
Northwestern UniversityRecruiting
-
University of PadovaActive, not recruiting
-
Meyer Children's Hospital IRCCSTerminated
Clinical Trials on Priorities
-
Yale UniversityPatient-Centered Outcomes Research Institute; Robert Wood Johnson Foundation; The John A. Hartford Foundation and other collaboratorsCompletedMultiple Chronic Conditions
-
Indiana UniversityNational Institutes of Health (NIH); National Institute on Aging (NIA)CompletedPatient Priorities Care Among Persons Living With Mild Cognitive Impairment and Dementia (IN-TX-PPC)Dementia | Mild Cognitive ImpairmentUnited States
-
University of North Carolina, Chapel HillYale University; National Institute on Aging (NIA); North Carolina Translational...Withdrawn
-
The Cleveland ClinicYale University; Donaghue Medical Research FoundationCompletedMultiple Chronic ConditionsUnited States
-
University of Alabama at BirminghamCompletedMultiple Chronic Conditions | Family MembersUnited States
-
Indiana UniversityNot yet recruitingTraumatic Brain Injury | TBI | Traumatic Brain Injury (TBI) PatientsUnited States
-
The University of Texas Medical Branch, GalvestonThe University of Texas Health Science Center, HoustonCompletedDementia | Multiple Chronic ConditionsUnited States
-
The University of Texas Health Science Center,...National Institute on Aging (NIA); National Center for Advancing Translational...RecruitingBreast Cancer SurvivorshipUnited States
-
VA Office of Research and DevelopmentCompletedMultiple Chronic Conditions | Decision Making, SharedUnited States
-
Western University, CanadaJohns Hopkins University; University of British Columbia; Canadian Institutes... and other collaboratorsCompletedDomestic ViolenceCanada