Actively Recruiting

Phase Not Applicable
Age: 13Years - 19Years
All Genders
NCT06819813

Project VIBE: Virtual Intervention for Binge Eating in Adolescents

Led by University of Pittsburgh · Updated on 2026-04-24

50

Participants Needed

2

Research Sites

97 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

N

Northwestern University

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Project VIBE: Virtual Intervention for Binge Eating in Adolescents

Who Can Participate

Age: 13Years - 19Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • BMI at or above the 75th percentile for age and sex
  • Recent loss of control eating and/or overeating with 3 or more episodes in the past 3 months
  • Have an email address, smartphone, and regular internet access
  • Willing and able to measure height and weight before enrollment
Not Eligible

You will not qualify if you...

  • More than 2 instances of compensatory behaviors (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 affecting weight or appetite or receiving treatment for eating or weight disorders
  • Have medical or psychiatric conditions significantly affecting eating or weight, except binge eating disorder
  • Developmental or cognitive delay preventing participation
  • Currently pregnant or lactating

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Northwestern University

Chicago, Illinois, United States, 60208

Actively Recruiting

2

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

E

Erin R Stalvey, MPH

CONTACT

A

Andrew Tyler, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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