Mothers and CareGivers Investing in Children Study 2.0
NCT06719102 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 266
Last updated 2025-04-29
Summary
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
- Childhood Obesity Prevention
- Parenting Behavior
- Infant Growth
Interventions
- BEHAVIORAL
-
MAGIC-FEED
Parents will be provided with responsive feeding coaching to help them recognize hunger and satiety cues and nutrition coaching that includes bottle-/breast-feeding and complementary feeding in alignment with the Dietary Guidelines. The intervention is delivered via virtual visits, binder, website and newsletters.
- BEHAVIORAL
-
MAGIC-SAFE
Parents will be provided with information about age-appropriate safety topics, including safe sleeping, car seats, baby-proofing, etc. The intervention is delivered via virtual visits, binder, website and newsletters.
Sponsors & Collaborators
-
National Institutes of Health (NIH)
collaborator NIH -
University of Texas at Austin
lead OTHER
Principal Investigators
-
Elizabeth Widen, PhD, RD · UT Austin
-
Deborah Jacobvitz, PhD · UT Austin
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 0 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-02-13
- Primary Completion
- 2028-12-31
- Completion
- 2029-12-31
Countries
- United States
Study Locations
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