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
Sponsors and collaborators
3-C Institute for Social Development
Lead sponsor
Washington University School of Medicine
Collaborator
University at Buffalo
Collaborator