Eating Disorder Symptom Clinical Trial
Official title:
Feasibility of Online Exposure Therapy and Self-compassion Interventions for Eating and Body Image Concerns Among Young Adult Women
| NCT number | NCT04665167 |
| Other study ID # | 168743 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | January 13, 2021 |
| Est. completion date | March 30, 2021 |
| Verified date | August 2020 |
| Source | University of Sheffield |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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.
| Status | Completed |
| Enrollment | 30 |
| Est. completion date | March 30, 2021 |
| Est. primary completion date | February 26, 2021 |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | 18 Years and older |
| Eligibility | 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 |
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | University of Sheffield | Sheffield |
| Lead Sponsor | Collaborator |
|---|---|
| University of Sheffield |
United Kingdom,
Franko DL, Striegel-Moore RH. The role of body dissatisfaction as a risk factor for depression in adolescent girls: are the differences Black and White? J Psychosom Res. 2002 Nov;53(5):975-83. Review. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Number of participants recruited | 30 participants | will measure upon study termination (estimated at 2-3 months) | |
| Secondary | The rate of completion | assessed by the percentage of participants who complete the study questionnaires | will measure upon study termination (estimated at 2-3 months) |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
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