An Intervention for Eating and Body Image Concerns Among Young Adult Women

Sponsor
University of Sheffield (Other)
Overall Status
Completed
CT.gov ID
NCT04665167
Collaborator
(none)
30
1
2
2.5
12

Study Details

Study Description

Brief Summary

The primary aim of the current study is to assess acceptability and feasibility of online body image exposure and self-compassion interventions before conducting a larger RCT.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Body image exposure
  • Behavioral: Self-compassion
N/A

Detailed Description

This study will determine the feasibility and effectiveness of delivering an online therapy for eating pathology and body image disturbance. It will address body image and eating pathology in a non-clinical group of young adult women, who are at risk of developing such problems . The feasibility study will determine whether there are any difficulties that would need to be addressed in recruitment, online delivery and assessment of those treatments.

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Feasibility of Online Exposure Therapy and Self-compassion Interventions for Eating and Body Image Concerns Among Young Adult Women
Actual Study Start Date :
Jan 13, 2021
Actual Primary Completion Date :
Feb 26, 2021
Actual Study Completion Date :
Mar 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Body image exposure

Guided non-judgmental exposure, 40 minutes total

Behavioral: Body image exposure
Exposure therapy is a key element of evidence-based cognitive behaviour therapy for eating disorders . Body image exposure intervention involves deliberate, planned, and systematic exposure to the body image. Participants will be asked to stand so that they can see their whole body - far enough back. Participants will be asked to look at their bodies on screen. Participants will be continually encouraged by the facilitator for looking at and talking about the body parts.

Active Comparator: Self-compassion

8 Short self-compassion meditations, 40 minutes total

Behavioral: Self-compassion
The self-compassion intervention condition consists of Neff's self-compassion exercises. These exercises are part of the self-compassion intervention condition. Meditation text used in this study is obtained from the following link https://self-compassion.org/category/exercises/.

Outcome Measures

Primary Outcome Measures

  1. Number of participants recruited [will measure upon study termination (estimated at 2-3 months)]

    30 participants

Secondary Outcome Measures

  1. The rate of completion [will measure upon study termination (estimated at 2-3 months)]

    assessed by the percentage of participants who complete the study questionnaires

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Body shape questionnaire score > 25

  • Age ≥18

  • Self-identified women

  • Be able to use a computer and having an Internet connection and webcam

Exclusion Criteria:
  • Insufficient knowledge of English

  • Learning disability, severe mental illness or alcohol/substance dependence, history of self-injuries, current eating disorder, current clinical depression

  • Psychiatric illness requiring secondary care intervention

  • Male

  • Under 18 years old

  • Body mass index below 18.5

  • Currently undergoing psychological therapies

  • No access to a tablet or computer with an internet connection

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Sheffield Sheffield United Kingdom S1 2LT

Sponsors and Collaborators

  • University of Sheffield

Investigators

  • Principal Investigator: Fidan Turk, University of Sheffield

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
University of Sheffield
ClinicalTrials.gov Identifier:
NCT04665167
Other Study ID Numbers:
  • 168743
First Posted:
Dec 11, 2020
Last Update Posted:
Apr 8, 2021
Last Verified:
Aug 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Sheffield
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 8, 2021