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临床试验/NCT04810403
NCT04810403已完成不适用

An Open Trial Pilot Study of SOMEBODY, a Social Media-based Eating Disorder Prevention Program for College Women

Florida State University2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2021年3月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
8
试验地点
2
主要终点
Change in internalization of the thin ideal

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 18 to 25 years old
  • score in the top 50th percentile for time spent on social media each day

排除标准

  • <18 years or >25 years old
  • individuals who screen positive for a Diagnostic Statistical Manual-5 eating disorder on the Eating Disorder Diagnostic Scale

结局指标

主要结局

Change in internalization of the thin ideal

时间窗: Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline)

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

Acceptability of intervention

时间窗: 2 weeks

Acceptability will be evaluated with 7-point Likert scale ratings, with a score ≥5 indicating that participants found the intervention acceptable

Feasibility of intervention

时间窗: 2 weeks

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

次要结局

  • Change in dietary restraint(Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline))
  • Adherence to protocol - observed(Daily for the 14 days of the intervention)
  • Change in body image concerns(Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline))
  • Change in bulimic symptoms(Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline))
  • Change in disordered eating(Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline))
  • Change in social media use(Pre-intervention assessment to post-intervention assessment (or approximately 14 days from baseline))
  • Adherence to protocol - self-reported(2 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Pamela Keel

Professor

Florida State University

研究点 (2)

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