Sign in

NCT06728800Not yet recruiting

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

Source: ClinicalTrials.gov · Last updated 28 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
66 (estimated)
First submitted
6 Dec 2024
Start date
1 Oct 2026
Primary completion date
31 Jul 2027
Lead sponsor
3-C Institute for Social Development
Diseases
Obesity
NCT number
NCT06728800

What you commit to

  • Study type: Interventional
  • Planned participants: 66
  • From 1 Oct 2026 to the primary completion date, 31 Jul 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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)

Other

  • youth is unable to provide assent

Who the study is looking for

  • 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

Age in the registry: 6 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
3C Institute
Coordinator of this site? Confirm its status
DurhamUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.