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NCT06777888Active, not recruiting

Childhood Obesity Management Using Innovative Digital Technology

Source: ClinicalTrials.gov · Last updated 16 Jan 2025

Brief summary (registry, in English)

The project will evaluate the short- and long-term effects of a 10-week Family Healthy Living Program (FHLP). The program is designed for families with children ages 8-12 years old who are at risk for being above a healthy weight and who would like support with healthy living habits such as physical activity and healthy eating. Families will participate together, with both parents and children being involved in the program. FHLP participants will receive 9 weekly 2-hour online group sessions with a facilitation team as well as additional web-based resources. They will be compared to a control group of participating families who will be offered only the self-guided web-based resources. This will help us see the impact of offering facilitated FHLP group sessions versus only offering resources online. The FHLP is 10 weeks long, but participants will be followed for 12 months in total so that researchers can look at the long-term impact of participation. All participating families from both groups will be asked to complete surveys and provide child height and weight measurements at four timepoints: before beginning the program, immediately after completing the program, at 6-months post-program, and at 12-months post-program. Children will also be given FitBit activity watches to measure their daily step counts at each timepoint. Researchers will compare survey responses, child growth patterns, and FitBit step counts between the FHLP participants and the control group to see whether participating in the FHLP helps families improve their healthy living habits more than only offering a similar curriculum of healthy living resources online for families to access on their own.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
270 (actual)
First submitted
2 Dec 2024
Start date
15 Dec 2021
Primary completion date
May 2025
Lead sponsor
University of Victoria
Diseases
Obesity
NCT number
NCT06777888

What you commit to

  • Study type: Interventional
  • Participants enrolled: 270
  • From 15 Dec 2021 to the primary completion date, May 2025
  • 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

  • Any conditions that prevent children from being physically active.

Other

  • Children below the 85th percentile BMI.
  • The inability to communicate (speak, read, and write) in English.

Who the study is looking for

  • Children must be aged 8-12 years with at least one primary caregiver who agrees to participate with them. More than one child per parent will be able to participate if the child meets the inclusion criteria.
  • Children must have a BMI ≥ 85th percentile for age and sex.

Age in the registry: 8 years to 12 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Victoria
Coordinator of this site? Confirm its status
VictoriaCanadaUnknown status

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