The Bottle Study: Infant Weight Gain During Use of Novel Versus Typical Infant Feeding Bottles

Status

Terminated

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01526018

Enrollment

Registered

2012-02-03

Start date

2012-01-31

Completion date

2014-01-31

Last updated

2014-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infant Feeding Behavior

Keywords

Intake, Formula feeding

Brief summary

The purpose of this study is to pilot test whether a novel infant feeding bottle changes how much formula an infant drinks and how quickly he/she drinks it, as compared to meals provided in a standard bottle. Exclusively formula-fed infants and their caregiver will be provided with the novel feeding bottle and caregivers will be asked to acclimate their infant to this bottle during the next several weeks. Once acclimated, infants will undergo two weighed, timed, and videotaped test meals on two separate days; one with the novel bottle and one with their standard bottle, in random order. It is hypothesized that when the novel bottle is used, infants bottle will consume smaller meals and will have a longer meal duration, as compared to when a standard bottle is used.

Interventions

BEHAVIORALPodee bottle

Infants will acclimate to the Podee bottle over the course of several weeks. All infants will consume meals from the Podee and their usual bottles.

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

1 Months to 6 Months

Healthy volunteers

Yes

Inclusion criteria

* healthy, exclusively formula-fed infants aged 1-6 months at enrollment; * parent must be at least 19 years of age, able to understand written and verbal English, and provide daytime care for the infant at least 4 days per week.

Exclusion criteria

* born \< 37 weeks; * birth weight \< 2500g or \> 4000g; * current weight \< 10th percentile for age; * hospitalization \> 72 hours following birth or any hospital admission since birth; * any health issue that could interfere with feeding and/or growth; * use of complementary foods; * inability or unwillingness to comply with study-related procedures.

Design outcomes

Primary

Measure	Time frame	Description
Food intake	2 weeks	Rate of intake, volume of intake, duration of meal

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026