A Single Session Community-Based Body Empowerment Session

Sponsor
Equip Health (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT06139601
Collaborator
(none)
75
1
16

Study Details

Study Description

Brief Summary

This present study will examine the effectiveness of a single session, virtually delivered body empowerment program for decreasing participants thin ideal internalization. The intervention asks participants to identify cultural norms surrounding appearance and attractiveness, then challenge these ideals. Participants will answer questions about thin ideal internalization before and after the program.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: single session intervention
N/A

Detailed Description

A body empowerment program rooted in the psychological theory of cognitive dissonance has been shown to be effective to reduce the value of the thin beauty ideal. This theory proposes that humans are motivated to maintain consistency in their beliefs and actions, and inconsistencies will result in psychological discomfort (or cognitive dissonance). A shift in beliefs or actions is required to resolve this discomfort and maintain consistency. However, the accessibility of this program is lacking. The proposed study will examine the effectiveness of a single session, virtually delivered body empowerment program designed to create cognitive dissonance by asking participants to identify cultural norms surrounding appearance and attractiveness, then challenge these ideals through a series of interactive activities in a fully virtual, self-paced module. Challenging these ideals (e.g., identifying how ideals represent very narrow identities and are informed by oppressive value systems, stating the psychological costs of trying to change your body to match ideals) theoretically creates cognitive dissonance in those who have internalized the value of pursuing those ideals. This dissonance is resolved through a reduced investment in the ideals and then hypothesized to lead to more positive attitudes about body image, dieting, and other unhealthy weight control behaviors. The program consists of a single 45-minute self paced, interactive, virtual module. Primary assessments will be completed at pre-intervention and post-intervention.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
75 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
A Single Session Community-Based Body Empowerment Session
Anticipated Study Start Date :
Jan 1, 2024
Anticipated Primary Completion Date :
Jan 1, 2025
Anticipated Study Completion Date :
May 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Other: Body empowerment intervention program

All study participants will complete a single session body empowerment program.

Behavioral: single session intervention
A single session, self-paced body empowerment program. The program consists of a single 45-minute self paced, interactive, virtual module.

Outcome Measures

Primary Outcome Measures

  1. Change in thin ideal internalization [Pre intervention obtained prior to completing the intervention, and immediately following the intervention.]

    Sociocultural Attitudes Towards Appearance Questionnaire (SATAQ-4) questionnaire will be used to evaluate thin ideal internalization. Participants note their agreement or disagreement regarding beliefs about appearance on a 5-point Likert scale ranging from definitely disagree (1) to definitely agree (5). The thin ideal internalization subscale will be used. High scores indicate greater thin ideal internalization.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 18+ years of age

  • Able to reliably access internet

  • Can speak and read English

  • Completed the body empowerment program

Exclusion Criteria:
  • None

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Equip Health

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Equip Health
ClinicalTrials.gov Identifier:
NCT06139601
Other Study ID Numbers:
  • 1006
First Posted:
Nov 18, 2023
Last Update Posted:
Nov 18, 2023
Last Verified:
Nov 1, 2023
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

Study Results

No Results Posted as of Nov 18, 2023