Mothers and CareGivers Investing in Children Study 2.0
University of Texas at Austin · with National Institutes of Health (NIH) · NCT06719102
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 0 mo–90 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 266
- US sites recruiting
- 1
- Study start
- February 13, 2025
- Record last updated
- June 10, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study 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.
Being studied: MAGIC-FEED; MAGIC-SAFE
Conditions: Childhood Obesity Prevention; Parenting Behavior; Infant Growth
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 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.
Exclusion Criteria
- Infant diagnosed with major physical disabilities and/or medical condition that affects feeding and growth, and/or born \<37 weeks gestation.
- Infant experienced NICU stay >7 days.
- Twins, triplets, or other multiples.
- Mothers and/or other caregivers younger than 18 years old.
- 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.
Recruiting US locations
Dell Pediatric Research Institute
Austin, TX 78723
Site contact: Elizabeth Widen · widen.lab@austin.utexas.edu
Study contacts (from the official record)
- Elizabeth Widen, PhD, RD · 512-471-0941 · widen.lab@austin.utexas.edu
- Deborah Jacobvitz, PhD
Similar studies in Texas
All weight loss studies in Texas →- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Study of Eloralintide (LY3841136) in Participants With Obesity or Overweight
Eli Lilly and Company
- Location
- San Antonio, TX
- Eligibility basics
- Ages 18–65
- RecruitingHealthy volunteersPhase 1
A Study of LY4174794 in Participants With Obesity or Overweight Who Are Otherwise Healthy
Eli Lilly and Company
- Location
- San Antonio, TX
- Eligibility basics
- Ages 18–65
- RecruitingHealthy volunteersPhase 1
A Study of Eloralintide (LY3841136) in Female Participants With Obesity or Overweight
Eli Lilly and Company
- Location
- Dallas, TX + 1 other US site
- Eligibility basics
- Ages 18–60 · Women only
- RecruitingHealthy volunteersPhase 1
A Study of LY4329090 in Participants With Obesity or Overweight Who Are Otherwise Healthy
Eli Lilly and Company
- Location
- Dallas, TX + 1 other US site
- Eligibility basics
- Ages 18–65