About this trial
Using a two-group randomized study design, this study aims to evaluate the effectiveness of the adapted family-centered mHealth tool on child BMI z-score (primary outcome), child dietary behaviors, and parental feeding practices, from baseline to 12-month follow-up, among 200 child-parent dyads. It is hypothesized that children in the experimental group will demonstrate larger BMI-z score improvements between baseline and 12-month follow-up compared to children in the comparison group.
Eligibility criteria
Qualifiers
self-identifies as Black/African-American and/or Latino
between ages 8 and 12 years (preadolescents) at time of scheduled baseline visits
reads and speaks in English
has a Body Mass Index percentile at or above 5% at baseline (categorized as healthy, overweight, or obese)
Disqualifiers
has allergies, food aversions, food disorders, or medications with side-effects that may impact participation in study
has a pacemaker or heart condition
in foster care
Trial design
Treatments tested in this trial
- Web-based comic and newsletters
- Didactic health information
Treatment groups
Sponsors and collaborators
Tufts University
Lead sponsor
Children's Aid, New York City
Collaborator
Washington University School of Medicine
Collaborator
Agency for Healthcare Research and Quality (AHRQ)
Collaborator
Hunter College of City University of New York
Collaborator
City University of New York, School of Public Health
Collaborator
University of Massachusetts, Amherst
Collaborator