Intervention INC: An Interactive Family-centered mHealth Tool to Reduce Obesity Risk in Urban Minority Preadolescents

Recruiting N/A Interventional Study
Obesity, Childhood
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
8 – 12
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
200 (estimated)
Sponsor
Tufts University · Other
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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 improvem…
Trial Locations
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Eligibility Criteria
Inclusion Criteria (child): * 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, …
Contacts

May May Leung, PhD, RDN

617-636-3676

maymay.leung@tufts.edu

CONTACT