Enhancing Social Connections Among Rural Community Members With Disordered Eating
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Social Support Single-Session Intervention.
- Who it may be relevant to
- Registry conditions: Eating Disorders (Excluding Anorexia Nervosa), Disordered Eating, Disordered Eating Behaviors, Eating Disorder Symptom. Basic parameters: 18 years — 100 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
This study is about testing a short program that uses social support to help people with disordered eating. The goal is to see if this program can help people build better habits and feel better about eating while reducing harmful symptoms. In the long run, this project wants to make it easier for people with eating problems to get help and recover, especially for those in rural areas or other groups who don't often get the care they need. Participants will complete self-report measures online, and complete a digital single-session program.
Interventions
- Behavioral Social Support Single-Session Intervention
Single-session intervention to increase self-efficacy, social support, help-seeking, and recovery-oriented behaviors to address disordered eating.
Primary outcome measures
- eating disorder symptoms [Time frame: 1 month post-intervention]
Secondary outcome measures (4)
- Help-seeking [Time frame: 1 month post-intervention]
- Self-efficacy [Time frame: 1 month post-intervention]
- Social support and sense of community [Time frame: 1 month post-intervention]
- Personal Growth [Time frame: 1 month post-intervention]
Eligibility criteria
Inclusion criteria
- Adult (18+ years old)
- disordered eating
- live in the United States of America
Exclusion criteria
- BMI below 18.5
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06788145 · IRB-FY2024-307