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Digital Family Program Tested for Childhood Obesity Behavioral Treatment

Tests a digital family-based behavioral program for children with obesity and their parents.

Plain-language title generated from the registry record
Registry title: Leveraging Interactive Digital Technology to Increase Access to Family-Based Behavioral Treatment for Childhood Obesity

Key facts

Where
Durham, United StatesSee the site

Where in United States

  • 3C InstituteDurham, United StatesNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
3-C Institute for Social Development
Trial code
NCT06728800
Record updated
28 September 2026
Original description
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.Read full original descriptionShow less

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

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.

Inclusion: must be youth between the ages of 6 and 17; must have a body mass index (BMI) percentile greater than or equal to the 85th 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; the participating caregiver must have a body mass index (BMI) of 25 or greater; youth and caregiver must be English proficient; family must have reliable internet access and a working scale in the home.

Exclusion: co-morbid disorders that contraindicate weight loss (e.g., eating disorder); caregiver has a medical or psychiatric condition in which weight loss is contraindicated (e.g., pregnancy); youth is unable to provide assent.

ClinicalTrials.gov NCT06728800