Intervention to prevent childhood obesity through caregiver education
Mothers and CareGivers Investing in Children: MAGIC 2.0
This study is testing two programs to see if teaching caregivers better nutrition and feeding practices can help prevent obesity in infants during their first year of life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 266 (estimated) |
| Ages | 0 Years to 90 Years |
| Sex | All |
| Sponsor | University of Texas at Austin Academic / other |
| Locations | 2 sites (Austin, Texas and 1 other locations) |
| Trial ID | NCT06719102 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of two interventions, MAGIC-FEED and MAGIC-SAFE, on improving parenting behaviors and infant health outcomes related to obesity prevention. Using a longitudinal, randomized control trial design, the study will assess the impact of these interventions on infant body mass index z-scores (BMIZ) at 13 months, as well as caregiver nutrition knowledge and feeding practices. The trial leverages a virtual platform to enhance accessibility for caregivers, focusing on modifiable factors during the critical first year of life to support healthy growth and prevent obesity.
Who should consider this trial
Good fit: Ideal candidates include mothers or caregivers of singleton infants aged 3-9 weeks who live in the Austin metropolitan area and speak either English or Spanish.
Not a fit: Patients who may not benefit include those with infants diagnosed with major physical disabilities affecting feeding, or those who do not plan to remain in the Austin area for the next two years.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce the risk of obesity in infants and promote healthier eating behaviors in families.
How similar studies have performed: Previous studies have shown some success with similar interventions, but this approach utilizing a virtual platform is relatively novel.
Eligibility criteria
Show full inclusion / exclusion 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.
Where this trial is running
Austin, Texas and 1 other locations
- Sarah M. & Charles E. Seay Building — Austin, Texas, United States (Not_yet_recruiting)
- Dell Pediatric Research Institute — Austin, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Elizabeth Widen, PhD, RD — UT Austin
- Study coordinator: Elizabeth Widen, PhD, RD
- Email: widen.lab@austin.utexas.edu
- Phone: 512-471-0941
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.