Assessing Better Bottles for Babies
Completed · Not applicable
Conditions studied: Pediatric Obesity, Weight Gain Trajectory, Infant Obesity
In brief
This study will use a 2 x 2 factorial design to test impact of two intervention strategies (bottle size and bottle opacity) on infant weight gain.
Key facts
- Study ID
- NCT06357299
- Run by
- Duke University
- People needed
- 5
- Starts
- 2025-05-28
- Expected to finish
- 2026-03-25
- Last updated by the study team
- 2026-07-09
Who can join
Age: 0 and older, up to 0. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Child is 3 days old to 1 month old
- Greater than 37 weeks gestational age at birth
- Birth weight greater than 3% for sex-specific WHO growth standard
- Caregiver must plan to use local clinic as infant's primary medical home for first 6 months of life
- Caregiver must speak English or Spanish as primary preferred language
- Caregiver age 18 years or older
- Caregiver must agree to use intervention bottles assigned during randomization and agree to stop using their existing bottles during the study period
You may not qualify if…
- Multiple gestation
- Significant congenital anomaly or acquired or inherited condition directly affecting feeding, physiology, metabolism, or growth
- Feeding with soy-based, hydrolyzed, lactose-reduced, or elemental formula
- Weight loss greater than 95% for population reference in the first two weeks of life
Where it is running
- Duke University — Durham, North Carolina, United States
Full record on ClinicalTrials.gov
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