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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04810403
Other study ID # 00001960
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 29, 2021
Est. completion date April 22, 2022

Study information

Verified date May 2022
Source Florida State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to develop and evaluate the feasibility, acceptability, and preliminary evidence of potential efficacy of a social-media based intervention to reduce risk factors for eating disorders in college women.


Description:

Previous research supports an association between specific aspects of social media use and increased eating pathology in correlational designs and that specific aspects of social media use cause increases in risk factors for eating disorders. The aim of the current project is to determine whether social media use can be altered to cause decreases in eating disorder risk factors. To accomplish this, college women will be recruited to participate in an open trial of a pilot program that adapts activities used within evidence-based eating disorder prevention programs to be used on social media platforms. The intervention is designed to target internalization of the thin ideal.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date April 22, 2022
Est. primary completion date April 22, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: - female - 18 to 25 years old - score in the top 50th percentile for time spent on social media each day Exclusion Criteria: - male - <18 years or >25 years old - individuals who screen positive for a Diagnostic Statistical Manual-5 eating disorder on the Eating Disorder Diagnostic Scale

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
SOMEBODY Eating Disorder Prevention Program
Participants will receive daily activities to complete on their most frequently used social media platform for 14 consecutive days. Daily activities have been adapted from the Body Project - an intervention that has been demonstrated to reduce internalization of the thin ideal and reduce risk for eating disorders. Examples of activities to be piloted include unfollowing social media accounts the participant perceives as reinforcing the thin-ideal and posting a selfie without makeup or editing. Based on feedback from participants, the intervention may be altered to improve acceptability, feasibility, and preliminary evidence of potential efficacy.

Locations

Country Name City State
United States Florida State University Psychology Department Tallahassee Florida

Sponsors (1)

Lead Sponsor Collaborator
Florida State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptability of intervention Acceptability will be evaluated with 7-point Likert scale ratings, with a score =5 indicating that participants found the intervention acceptable 2 weeks
Primary Feasibility of intervention Feasibility will be evaluated as the percentage of consented and enrolled participants who complete =10 of the 14 days of the intervention, with =80% indicating feasibility 2 weeks
Primary Change in internalization of the thin ideal The Sociocultural Attitudes Towards Appearance Questionnaire - 4 Revised (SATAQ-4R) Internalization Subscales will be used to measure internationalization of the thin ideal before and after the intervention. An effect size of d=.50 for within subject change in score will establish preliminary evidence of potential efficacy Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline)
Secondary Change in body image concerns The Eating Disorders Examination Questionnaire Weight and Shape Concerns subscales adapted for the past 7 days will be used to measure change in body image before and after the intervention Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline)
Secondary Change in dietary restraint The Eating Disorders Examination Questionnaire Dietary Restraint subscale adapted for the past 7 days will be used to measure change in dietary restraint before and after the intervention Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline)
Secondary Change in bulimic symptoms The Eating Disorders Examination Questionnaire Self-Reported Bulimic Symptom Composite Score adapted for the past 7 days will be used to measure change in bulimic symptom frequency before and after the intervention Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline)
Secondary Change in disordered eating The Eating Disorders Examination Questionnaire Global Score adapted for the past 7 days will be used to measure change in disordered eating before and after the intervention Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline)
Secondary Change in social media use The Social Media Use Questionnaire items assessing frequency and type of engagement with social media will be used to measure change in social media use before and after the intervention Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline)
Secondary Adherence to protocol - self-reported The Social Media Use Questionnaire items assessing adherence to daily social media activities will be used to measure self-reported adherence after the intervention 2 weeks
Secondary Adherence to protocol - observed With participant consent, a research assistant will follow the social media account the participant plans to use for the SOMEBODY intervention and will complete a checklist on a daily basis (yes/no) on whether or not the participant completed the daily assignment Daily for the 14 days of the intervention
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