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NCT05794763 · ClinicalTrials.gov registry record · NA
The Body Project: Comparing the Effectiveness of an In-person and Virtually Delivered Intervention.
A NA study of Eating Disorders, sponsored by Stanford University.
- Completed
- Registry status
- NA
- Development phase
- 69
- Enrollment target
- 2
- Study locations
NCT05794763: Completed NA study of Eating Disorders, sponsored by Stanford University.
NCT05794763 is a NA study of Eating Disorders that has completed, run by Stanford University. The registered enrollment target is 69 participants, below the 321-participant average among 37 other Eating Disorders trials with a reported enrollment target (79% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05794763, a NA study of Eating Disorders, has completed, sponsored by Stanford University.
- COMPLETED
- Registry status
- NA
- Development phase
- 69 participants
- Enrollment target
- 2
- Study locations
Study Summary
This present study will compare the efficacy of in-person versus virtually-delivered Body Project groups. It will also evaluate whether this body acceptance class produces greater reductions in eating disorder risk factor symptoms (pursuit of the thin ideal, body dissatisfaction, dieting, dietary restraint, negative affect, eating disorder symptoms, and the future onset of eating disorders over a 3-month follow-up in this population. It will also evaluate the effectiveness of this body acceptance class's ability to impact social appearance anxiety, body compassion, and self-stigma surrounding attaining help.
Conditions Studied
Interventions
- BEHAVIORAL Peer Led Group Intervention
Study Locations (2)
California
- Stanford University - Palo Alto
Maryland
- St. Mary's College of Maryland - Saint Marys City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 69 participants |
| Start Date | 2022-03-31 |
| Est. Completion | 2024-03-05 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05794763
The ClinicalTrials.gov registry entry for NCT05794763 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 69 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 321-participant average among 37 other Eating Disorders trials with a reported enrollment target (79% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Eating Disorders appearing as the primary indexed condition, and to 1 intervention - of which Peer Led Group Intervention is the first listed.
NCT05794763 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, Maryland.
Frequently Asked Questions
What is clinical trial NCT05794763 about?
NCT05794763 is a clinical study titled "The Body Project: Comparing the Effectiveness of an In-person and Virtually Delivered Intervention.". This present study will compare the efficacy of in-person versus virtually-delivered Body Project groups. It will also evaluate whether this body acceptance class produces greater reductions in eating disorder risk factor symptoms (pursuit of the thin ideal, body dissatisfaction, dieting, dietary re...
What is the current status of trial NCT05794763?
This trial is currently completed. It is a NA study. The enrollment target is 69 participants. The study started on 2022-03-31. Estimated completion is 2024-03-05.
What conditions does trial NCT05794763 study?
This clinical trial studies the following conditions: Eating Disorders.
What interventions are being tested in trial NCT05794763?
The interventions under investigation include: Peer Led Group Intervention (BEHAVIORAL).
Who is sponsoring clinical trial NCT05794763?
This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05794763 being conducted?
This trial has 2 study locations across California, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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