RECRUITING

Futuros Fuertes 2.0

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this study is to evaluate the impact of a primary care based intervention to promote optimal feeding, screen time and sleep practices among low-income Latino infants and toddlers. Infants and caregivers will receive brief health education and coaching sessions from health educators at primary care visits in the first two years of life as well as two text messages per week with health information and tips. Half of the participants will receive the Futuros Fuertes 2.0 intervention that includes health coaching and education on infant feeding, screen time and sleep (intervention group). The other half will receive health coaching and education on safety, home management of childhood illnesses, and promotion of language development (control group). We will look at the impact of the Futuros Fuertes 2.0 intervention on child BMI and various health behaviors.

Official Title

Futuros Fuertes 2.0 A Primary Care Based Intervention to Prevent Obesity Among Low-income Latino Children

Quick Facts

Study Start:2024-05-13
Study Completion:2028-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06398509

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:7 Days to 2 Months
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Parent/caregiver self identifies as Latino
  2. * Parent/caregiver speaks Spanish or English
  3. * Parent/caregiver intends to receive primary care for infant at participating clinic
  4. * Infant gestational age of 37 weeks or greater
  5. * Infant birthweight of 2600 grams or greater
  6. * For multiples (twins, triplets), one sibling will be chosen at random to participate
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Amy Beck, MD, MPH
CONTACT
415-476-3368
amy.beck@ucsf.edu

Principal Investigator

Amy Beck, MD, MPH
PRINCIPAL_INVESTIGATOR
University of California, San Francisco

Study Locations (Sites)

Children's Health Center San Francisco General Hospital
San Francisco, California, 94110
United States
Valley Health Center Sunnyvale
Sunnyvale, California, 94086
United States

Collaborators and Investigators

Sponsor: University of California, San Francisco

  • Amy Beck, MD, MPH, PRINCIPAL_INVESTIGATOR, University of California, San Francisco

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-05-13
Study Completion Date2028-12

Study Record Updates

Study Start Date2024-05-13
Study Completion Date2028-12

Terms related to this study

Additional Relevant MeSH Terms

  • Obesity, Childhood