An Intervention for Eating and Body Image Concerns Among Young Adult Women
- Conditions
- Body Image DisturbanceEating Disorder Symptom
- Interventions
- Behavioral: Self-compassionBehavioral: Body image exposure
- Registration Number
- NCT04665167
- Lead Sponsor
- University of Sheffield
- 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.
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 30
- Body shape questionnaire score > 25
- Age ≥18
- Self-identified women
- Be able to use a computer and having an Internet connection and webcam
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Self-compassion Self-compassion 8 Short self-compassion meditations, 40 minutes total Body image exposure Body image exposure Guided non-judgmental exposure, 40 minutes total
- Primary Outcome Measures
Name Time Method Number of participants recruited will measure upon study termination (estimated at 2-3 months) 30 participants
- Secondary Outcome Measures
Name Time Method 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
Trial Locations
- Locations (1)
University of Sheffield
🇬🇧Sheffield, United Kingdom