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Recruiting Not applicable NCT06819813

Project VIBE: Virtual Intervention for Binge Eating in Adolescents

No applicable phase (e.g. observational)
Conditions: Obesity Binge-Eating Disorder Binge Eating

Sponsor: University of Pittsburgh

trial.available_in: БГ
Overview
The aim of this project is to pilot test a novel mobile app intervention for adolescents with dysregulated eating behaviors and elevated weight status. This intervention will incorporate evidence-informed strategies targeting self-regulation into cognitive-behavioral treatment for maladaptive eating. Adolescents will use the app for 16 weeks and provide feedback on its usability and effectiveness in managing dysregulated eating.
Description
This trial is part of a multi-phase project to create and test a mobile app intervention aimed at helping teenagers regulate their eating behaviors. Participation in this trial involves the following: 1. Adolescents and their parent are asked to attend a virtual assessment visit, where they will provide consent and complete questionnaires on eating-related thoughts and behaviors, mood, and experience with technology. The adolescent will also be asked to complete a semi-structured interview and provide height/weight measurements. 2. Eligible adolescents are then asked to complete a test-run week to make sure the trial is a good fit for them. They will be mailed a FitBit to wear continuously during the test-run week and a Smartscale to record their weight. They will also complete three 24-hour food recalls with a member of the research team during this week. Depending on engagement, the adolescent may or may not be invited to participate in the 16-week trial. 3. Adolescents eligible for the trial will use the VIBE app (Virtual Intervention for Binge Eating) and receive coaching for 16 weeks. Participants will also be asked to download an app that will help them with skill building and problem solving through short tasks/games, to be used while they are participating in the 16-week intervention. 4. Throughout the trial, adolescents will be invited to complete 3 additional assessment visits: "mid-point" or 8 weeks after starting the intervention, "post-intervention" at the end of the 16-week intervention, and "follow-up" 4 months after completing the intervention. These study assessments will include an interview, a weight measurement using the Smartscale, Fitbit usage for one week, up to 3 dietary recall phone calls, computerized tasks to assess how they think and solve problems, and online surveys. Each assessment will take about 90 - 120 minutes to complete.
Who can participate
Inclusion Criteria: * BMI≥75th percentile for their age and sex * Report recent loss of control eating and/or overeating (≥3 episodes of either type of eating behavior in the past 3 months) * Have an email address, Smartphone, and regular access to the internet * Be willing and able to measure their height and weight prior to study enrollment Exclusion Criteria: * Report more than 2 instances of compensatory behavior (e.g. diuretics, laxatives, vomiting, driven exercise) in the past 3 months * Not fluent in English at a third-grade reading level or higher * Currently taking medications known to affect weight or appetite or concurrently involved in treatment for eating or weight disorders * Meet criteria for a medical or psychiatric condition (e.g., diabetes, bulimia nervosa) known to significantly affect eating or weight, aside from binge eating disorder * Developmental or cognitive delay precluding participation in the intervention * Currently pregnant or lactating
Interventions
Feasibility/Efficacy Testing
BEHAVIORAL
Locations 2
United States (2)
Northwestern University
Chicago , Illinois
University of Pittsburgh
Pittsburgh , Pennsylvania
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
13 Years
Maximum age
19 Years
Healthy volunteers
No
Start date
14.07.2025
Completion date
30.05.2027
Registry ID
NCT06819813
Source
clinicaltrials.gov
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