Actively Recruiting

Phase Not Applicable
Age: 2Years +
All Genders
Healthy Volunteers
NCT05606731

Family Intervention to Prevent Childhood Obesity

Led by University of California, Los Angeles · Updated on 2025-03-10

182

Participants Needed

1

Research Sites

164 weeks

Total Duration

On this page

Sponsors

U

University of California, Los Angeles

Lead Sponsor

U

University of California, Merced

Collaborating Sponsor

AI-Summary

What this Trial Is About

Consumption of sweetened beverages, media-viewing, and physical activity patterns are often established during early childhood, and family-based obesity interventions show effectiveness in shaping healthy behaviors and weight outcomes for young children, including Latino children. Missing from these interventions, however, are methods to increase accessibility and dissemination to multiple family caregivers. The proposed work will use a randomized study design to evaluate the impact a family-based early childhood obesity intervention for Latino families that incorporates evidence-based strategies of in-person childhood obesity interventions, mobile phones, and leverages important determinants of Latino health (e.g. familism, language) in order to decrease ethnic disparities in childhood obesity and cardiovascular risk.

CONDITIONS

Official Title

Family Intervention to Prevent Childhood Obesity

Who Can Participate

Age: 2Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult caregivers who self-identify as Latino
  • Caregivers of a 2- to 5-year-old child or grandchild who is overweight or obese (BMI > 85th percentile for age and sex)
  • Caregivers who live with or care for the child at least 20 hours per week
  • Caregivers who speak Spanish or English
  • Caregivers able and willing to participate, as determined by assessment
  • Caregivers who agree to complete baseline, 1-, 6-, and 12-month data collection
Not Eligible

You will not qualify if you...

  • Caregivers of children with medical conditions related to overweight, such as Prader-Willi Syndrome
  • Caregivers of children currently taking weight loss medication
  • Caregivers of children participating in a weight loss program

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Head Start

Los Angeles, California, United States, 90670

Actively Recruiting

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Research Team

A

Alma D Guerrero, MD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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