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NCT06719102Recruiting

Mothers and CareGivers Investing in Children Study 2.0

Mothers and CareGivers Investing in Children: MAGIC 2.0

Source: ClinicalTrials.gov · Last updated 10 Jun 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
266 (estimated)
First submitted
23 Oct 2024
Start date
13 Feb 2025
Primary completion date
31 Dec 2028
Lead sponsor
University of Texas at Austin
Diseases
Obesity
NCT number
NCT06719102

What you commit to

  • Study type: Interventional
  • Planned participants: 266
  • From 13 Feb 2025 to the primary completion date, 31 Dec 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Infant diagnosed with major physical disabilities and/or medical condition that affects feeding and growth, and/or born \<37 weeks gestation.

Age

  • Mothers and/or other caregivers younger than 18 years old.

Other

  • Infant experienced NICU stay \>7 days.
  • Twins, triplets, or other multiples.
  • Mothers that do not consent to being video recorded with their baby.
  • Families that do not speak either English or Spanish will be excluded from this study. Families that only speak English or Spanish, or families that speak English or Spanish and another language, will be accepted.
  • Do not plan to remain in Austin area for the next two years.

Who the study is looking for

  • A singleton infant 3-9 weeks of age, born ≥37 weeks gestation.
  • The mother and other caregiver must be at least 18 years of age.
  • The infant must live with the mother.
  • Lives within the Austin metropolitan area.
  • English or Spanish speaking.
  • The primary caregiver must identify as the mother.

Age in the registry: 0 years to 90 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sarah M. & Charles E. Seay Building
Coordinator of this site? Confirm its status
AustinUnited StatesNot yet recruiting
Dell Pediatric Research Institute
Coordinator of this site? Confirm its status
AustinUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.