Leveraging Interactive Digital Technology to Increase Access to Family-Based Behavioral Treatment for Childhood Obesity

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6+
Sponsor3-C Institute for Social Development

About this trial

The primary goal of this SBIR Direct to Phase II is to expand upon the existing training platform to create an "all-in-one" digital product, FBT 2.0, that offers an integrated suite of intervention components, including (a) dynamic, personalized, self-paced program for children and parent/caregivers; (b) e-training and ongoing support for interventionists; and (c) family engagement and monitoring tools for interventionists. Investigators will create a comprehensive, e-learning digital intervention with engaging, interactive, and personalized online tools for youth and their parents/caregivers that are integrated into the broader interventionist platform.

Eligibility criteria

Qualifiers

must be youth between the ages of 6 and 18

must have a body mass index (BMI) percentile greater than or equal to the 95th BMI percentile for age and sex

must have one caregiver participate, who is at least 18 years of age and lives with the child at least 50% of the time.

Disqualifiers

co-morbid disorders that contraindicate weight loss (e.g., eating disorder).

Trial design

Treatments tested in this trial

  • FBT 2.0
  • Information-and-referral

Treatment groups

140 Participants
are divided into 2 treatment groups

Sponsors and collaborators

3-C Institute for Social Development

Lead sponsor

Washington University School of Medicine

Collaborator

University at Buffalo

Collaborator