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NCT04265794Completed

A Cluster Randomized Trial of the H2GO! Program

Preventing Childhood Obesity Through Youth Empowerment: A Cluster Randomized Trial of the H2GO! Program

Source: ClinicalTrials.gov · Last updated 16 Oct 2026

Brief summary (registry, in English)

This proposal involves a collaboration with the Massachusetts Alliance of Boys and Girls Clubs. The goal is to evaluate the efficacy of youth empowerment intervention targeting sugar-sweetened beverage consumption on childhood obesity among youth. The 12-session 6-week intervention consists of health and narrative sessions and youth-led activities. For this cluster randomized controlled trial (RCT) at 10 sites, the investigators plan to recruit 45 parent-child pairs per site for a total of 450 parent-child pairs/dyads. The primary outcome is child participants' body mass index (BMI) z scores. Secondary outcomes include children's sugar-sweetened beverage intake, water intake, and youth empowerment. Change in outcomes over time among participants in the intervention sites will be compared to change in outcomes over time among participants

Status (registry)
Completed
Study type
Interventional
Enrollment
820 (actual)
First submitted
10 Feb 2020
Start date
22 Oct 2020
Primary completion date
15 Jun 2025
Lead sponsor
Boston University
Diseases
Obesity
NCT number
NCT04265794

What you commit to

  • Study type: Interventional
  • Participants enrolled: 820
  • From 22 Oct 2020 to the primary completion date, 15 Jun 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.

Criteria the registry did not label

  • Child participant inclusion criteria
  • Ages 9-12 years
  • Current member at a BGC study site
  • Able to understand and communicate in English
  • Able and willing to provide assent
  • Parental/caregiver permission to participate
    • Child participant exclusion criteria - Has a medical condition that limits ability to change beverage consumption behaviors
    • Parent participant inclusion criteria
  • Parent or caregiver to a child member at a BGC study site
  • 18 years or older
  • able to understand and communicate in English
  • able and willing to provide consent
  • no plans to change their child's BGC membership over the next 12 months
    • Parent participant exclusion criteria
    • \- has a medical condition that limits ability to change beverage consumption behaviors

Age in the registry: 9 years to - · Sex: All · Accepts 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
Boston University School of Public Health
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

Related publications

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