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Califormula Study: Calibrated Formula Feeding to Optimize Infant Growth

Primary Purpose

Overweight and Obesity

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Intervention
Sponsored by
Milton S. Hershey Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Overweight and Obesity

Eligibility Criteria

1 Day - 1 Month (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Term or Early Term (≥37 weeks), singleton infants
  • Infant birthweight ≥50th percentile based on the 2013 Fenton Growth Charts (which account for sex of child and gestational age at birth)
  • Infant without substantial neonatal morbidity that would affect feeding or weight gain (e.g. known chromosomal abnormality, metabolic disorder, cleft lip/palate, etc.)
  • Infant age ≤1 month
  • Mothers with pre-pregnancy body mass index ≥25 kg/m2
  • Mothers ≥18 years old
  • Parental plan to exclusively feed infant 19-20 kcal/ounce formula upon delivery or by the start of the intervention period ~1 month after delivery
  • Parental intention to have infant well child visits through age 6 months at a Division of Academic General Pediatrics practice site (Hope Drive, Elizabethtown, Nyes Road)
  • English speaking parent

Exclusion Criteria:

  • Infants who weigh less than their birthweight 21 days after delivery

Sites / Locations

  • Penn State Milton S. Hershey Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

The intervention arm is characterized by calibrated formula feeding recommendations. The intervention group parents will be given written instructions on infant hunger and satiety cues as well as copies of videos with guidance on bottle feeding and how to soothe fussy infants without feeding. N=30 meeting inclusion/exclusion criteria

The control arm will have ad lib feeds as per usual care. N=30 meeting inclusion/exclusion criteria

Outcomes

Primary Outcome Measures

Conditional Weight Gain Difference Between Study Groups

Secondary Outcome Measures

Conditional Weight Gain Difference Between Study Groups
Mean Weight-for-Length Z-score (WLZ) on World Health Organization Child Growth Standards
Growth Trajectory (repeated measures of weight-for-length on World Health Organization Child growth standards) during the intervention period
Proportion of Infants with Overweight (Weight-for-Length ≥95th Percentile on World Health Organization Child Growth Standards)

Full Information

First Posted
October 11, 2021
Last Updated
October 18, 2023
Sponsor
Milton S. Hershey Medical Center
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), University of California, Los Angeles
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1. Study Identification

Unique Protocol Identification Number
NCT05104073
Brief Title
Califormula Study: Calibrated Formula Feeding to Optimize Infant Growth
Official Title
Califormula Study: Calibrated Formula Feeding to Optimize Infant Growth
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 20, 2022 (Actual)
Primary Completion Date
December 2, 2023 (Anticipated)
Study Completion Date
December 2, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Milton S. Hershey Medical Center
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), University of California, Los Angeles

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this voluntary research study is to determine if calibrated formula feeding recommendations can promote optimal growth for the first 6 months after birth for mothers with a pre-pregnancy body mass index of 25 or more.
Detailed Description
This pilot study seeks to determine if formula feeding recommendations that are calibrated using age and weight specific caloric intake recommendations can prevent excessive infant weight gain and reduce overweight in the first 6 months after birth among infants born to mothers with overweight prior to pregnancy electing to exclusively formula feed their infants. Calibrated formula feeding refers to adjusting the recommended daily caloric formula intake to account for weight status. A cohort of 60 infants will be recruited and randomized 2-3 weeks after birth to an intervention arm characterized by calibrated formula feeding recommendations or a control group with ad lib feeds as per usual care. Intervention group parents will also be given written instructions on infant hunger and satiety cues as well as copies of videos with guidance on bottle feeding and how to soothe fussy infants without feeding. The investigators hypothesize that the calibrated formula intake intervention will reduce rapid infant gain and overweight during infancy resulting in lower weight-for-length at age 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A cohort of 60 infants will be recruited and randomized 2-3 weeks after birth to an intervention arm characterized by calibrated formula feeding recommendations or a control group with ad lib feeds as per usual care.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
The intervention arm is characterized by calibrated formula feeding recommendations. The intervention group parents will be given written instructions on infant hunger and satiety cues as well as copies of videos with guidance on bottle feeding and how to soothe fussy infants without feeding. N=30 meeting inclusion/exclusion criteria
Arm Title
Control
Arm Type
No Intervention
Arm Description
The control arm will have ad lib feeds as per usual care. N=30 meeting inclusion/exclusion criteria
Intervention Type
Behavioral
Intervention Name(s)
Intervention
Intervention Description
Provided with educational materials, guidelines and instructions.
Primary Outcome Measure Information:
Title
Conditional Weight Gain Difference Between Study Groups
Time Frame
Between birth and 6 months
Secondary Outcome Measure Information:
Title
Conditional Weight Gain Difference Between Study Groups
Time Frame
During the intervention period spanning Ages 1-6 Months
Title
Mean Weight-for-Length Z-score (WLZ) on World Health Organization Child Growth Standards
Time Frame
1 time point at age 6 Months
Title
Growth Trajectory (repeated measures of weight-for-length on World Health Organization Child growth standards) during the intervention period
Time Frame
Spanning ages 1-6 months
Title
Proportion of Infants with Overweight (Weight-for-Length ≥95th Percentile on World Health Organization Child Growth Standards)
Time Frame
1 time point at age 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
1 Month
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Term or Early Term (≥37 weeks), singleton infants Infant birthweight ≥50th percentile based on the 2013 Fenton Growth Charts (which account for sex of child and gestational age at birth) Infant without substantial neonatal morbidity that would affect feeding or weight gain (e.g. known chromosomal abnormality, metabolic disorder, cleft lip/palate, etc.) Infant age ≤1 month Mothers with pre-pregnancy body mass index ≥25 kg/m2 Mothers ≥18 years old Parental plan to exclusively feed infant 19-20 kcal/ounce formula upon delivery or by the start of the intervention period ~1 month after delivery Parental intention to have infant well child visits through age 6 months at a Division of Academic General Pediatrics practice site (Hope Drive, Elizabethtown, Nyes Road) English speaking parent Exclusion Criteria: Infants who weigh less than their birthweight 21 days after delivery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ian Paul, MD, MSc
Organizational Affiliation
Penn State College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Penn State Milton S. Hershey Medical Center
City
Hershey
State/Province
Pennsylvania
ZIP/Postal Code
17033
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
This may change in the future depending on results, although all individual participant data will be de-identified.

Learn more about this trial

Califormula Study: Calibrated Formula Feeding to Optimize Infant Growth

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