Actively Recruiting
Mothers and CareGivers Investing in Children Study 2.0
Led by University of Texas at Austin · Updated on 2025-04-29
266
Participants Needed
2
Research Sites
254 weeks
Total Duration
On this page
Sponsors
U
University of Texas at Austin
Lead Sponsor
N
National Institutes of Health (NIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The study will use a longitudinal, randomized control trial design to determine intervention impact on parent and child behaviors, and infant health. The two intervention groups include: 1) MAGIC-FEED+; and 2) MAGIC-SAFE. This trial is an efficacy trial of the MAGIC-FEED and MAGIC-SAFE program that has been successfully implemented with families as part of the MAGIC 1.0 program trial (IRB#: 2015040017). * The primary aim is to investigate each intervention's impact on infant BMIZ at 13 months. * The investigators will also assess the effect of MAGIC-FEED on caregiver nutrition knowledge and feeding practices, responsive feeding, infant diet, and child self-regulatory abilities and assess how these factors impact child self-regulation of eating and adiposity. * Finally, the investigators will determine if the interventions demonstrate the factors necessary to be a successful intervention as determined by the RE-AIM and PRISM frameworks.
CONDITIONS
Official Title
Mothers and CareGivers Investing in Children Study 2.0
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Infant is a singleton aged 3 to 9 weeks, born at or after 37 weeks gestation
- Mother and other caregiver are at least 18 years old
- Infant lives with the mother
- Family lives within the Austin metropolitan area
- Caregiver speaks English or Spanish
- Primary caregiver identifies as the mother
You will not qualify if you...
- Infant has major physical disabilities or medical conditions affecting feeding and growth
- Infant born before 37 weeks gestation
- Infant stayed in NICU for more than 7 days
- Infant is part of twins, triplets, or other multiples
- Mothers or caregivers younger than 18 years old
- Mothers do not consent to video recording with their baby
- Families who do not speak English or Spanish
- Families not planning to stay in the Austin area for the next two years
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Sarah M. & Charles E. Seay Building
Austin, Texas, United States, 78712
Not Yet Recruiting
2
Dell Pediatric Research Institute
Austin, Texas, United States, 78723
Actively Recruiting
Research Team
E
Elizabeth Widen, PhD, RD
CONTACT
D
Deborah Jacobvitz, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here