REFINE: Responsive Feeding of Infants With Expressed Milk

• Sponsor: Mount Saint Vincent University (Other)
• Overall Status: Terminated
• CT.gov ID: NCT04041505
• Collaborator: University of Prince Edward Island (Other), Queen's University (Other)
• Enrollment: 9
• Location: 1
• Arms: 2
• Actual Duration (Months): 7.5
• Patients Per Site Per Month: 1.2

Study Details

Study Description

Brief Summary

Nova Scotia has among the lowest breastfeeding rates in Canada, with less than one quarter of infants receiving Health Canada's recommended 6 months of exclusive breastfeeding. Compared with feeding formula, breastfeeding has been linked with a number of health advantages, including fewer infections, higher IQ, and a lowered risk of obesity later in life.

How infants consume human milk is changing. Pumping milk has grown in popularity in recent years because some mothers may feel stigmatized breastfeeding, especially in public, but also because it allows other caregivers to help with feeding. Although pumped human milk is considered equal to breastfeeding, there is very little research in this area, especially around responsive feeding and later health outcomes. Since pumped milk is fed from a bottle, the health benefits may be lost (for instance, this may impact a baby's ability to understand if s/he is hungry or full).

The primary aim of this study is to determine if the volume of human milk an infant consumes differs if they consume milk from a bottle versus the breast. The investigators will conduct a cross-over trial in which 62 mother-infant pairs will be randomized to feed at the breast or from a bottle for 24 hours, have a 24 hour wash-out period, and then 'cross-over' to another 24 hour session with the opposite 'treatment.' The volume of milk consumed at each feed within the 24 hour window (via indirect weighing, or weighing the baby before and after eating) will be recorded to determine if there are differences in milk consumption. Mother-infant pairs will complete this 3-day study three times, at 6 weeks, 4 months, and 6 months.

Information from this study will help to better understand current infant feeding practices in Nova Scotia, and the potential role this plays in future health outcomes. Evidence from this study may help to identify means of improving feeding practices and promoting human milk as the main food for Nova Scotian infants, setting them on a path for the best start in life.

Condition or Disease	Intervention/Treatment	Phase
Human Milk; Breastfeeding; Feeding Behavior	Behavioral: (feeding modality)	N/A

Detailed Description

See attached full protocol document for full details.

Study Design

• Study Type: Interventional
• Actual Enrollment: 9 participants
• Allocation: Randomized
• Intervention Model: Crossover Assignment
• Intervention Model Description: This is a modified, randomized cross-over study. The 'intervention' in this study is simply feeding infants using one of two modalities that are already familiar to the mother and infant: feeding mother's milk from the breast and from a bottle. At each timepoint (6 weeks, 4 months, 6 months) infants will: be randomized using a balanced design (to control for order effect) to consume human milk from a bottle or from the breast for 24 hours; will then undergo a wash-out period in which they will be fed human milk as they usually would for 24 hours; then will complete the second 'treatment' (bottle or breast) for 24 hours. Due to the nature of the intervention, this study will not be blinded. We aim to recruit 62 mother-infant pairs (= 124 participants in total).This is a modified, randomized cross-over study. The 'intervention' in this study is simply feeding infants using one of two modalities that are already familiar to the mother and infant: feeding mother's milk from the breast and from a bottle. At each timepoint (6 weeks, 4 months, 6 months) infants will: be randomized using a balanced design (to control for order effect) to consume human milk from a bottle or from the breast for 24 hours; will then undergo a wash-out period in which they will be fed human milk as they usually would for 24 hours; then will complete the second 'treatment' (bottle or breast) for 24 hours. Due to the nature of the intervention, this study will not be blinded. We aim to recruit 62 mother-infant pairs (= 124 participants in total).
• Masking: None (Open Label)
• Primary Purpose: Other
• Official Title: Feeding Infants in Nova Scotia: an Exploratory Analysis of Responsive Feeding With Mother's Milk
• Actual Study Start Date: Aug 15, 2019
• Actual Primary Completion Date: Mar 30, 2020
• Actual Study Completion Date: Mar 30, 2020

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: Breastfeeding Infant consumes mother's milk directly from the breast.	Behavioral: (feeding modality); The intervention is a change in feeding modality: in both arms, infant's will consume mother's milk. The difference in arms is the modality in which human milk is consumed: either directly from the breast, or from a bottle.
Experimental: Bottle-feeding Infant consumes mother's expressed milk from a bottle.	Behavioral: (feeding modality); The intervention is a change in feeding modality: in both arms, infant's will consume mother's milk. The difference in arms is the modality in which human milk is consumed: either directly from the breast, or from a bottle.

Outcome Measures

Primary Outcome Measures

1. Volume of milk consumption [24 hours]

   To assess if the volume of human milk consumed by infants differs by feeding modality (bottle feeding human milk versus breastfeeding), assessed as overall milk volume consumed over 24 hours, measured by indirect weighs at each feed during a 24-hour period.

Secondary Outcome Measures

1. Infant growth [Between 6 weeks and 6 months]

   To determine whether change in infant anthropometric measurements (length in cm, weight in kg, head circumference in cm) and growth rates (weight-for-age [WAZ], length-for-age [LAZ], weight-for-length [WLZ], BMI-for-age z-scores [BAZ]; all computed as z-scores) differ by self-reported usual feeding modality among infants exclusively consuming human milk.

2. Responsive feeding behaviors [Between 6 weeks and 6 months]

   To objectively assess responsiveness of infant feeding practices, both at the breast and during bottle-feeding of human milk, by video-recording feeding sessions in participant's homes.

Other Outcome Measures

1. Feeding environment [Between 6 weeks and 6 months]

   To gain a better understanding of current infant feeding practices, including responsive feeding, among caregivers in the Halifax Regional Municipality, contextualize why women are pumping, and gain insight around how human milk is handled, stored, and prepared through open-ended one-on-one interviews with mothers.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 19 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion criteria: Mother-infant dyads are eligible to participate if:

• mother is aged 19 years or older,

• dyads currently live in the Halifax Regional Municipality in Nova Scotia,

• mother has no chronic diseases,

• the baby is a healthy singleton baby who is younger than 6 weeks of age, and is fed mother's milk directly from the breast and from a bottle,

• mother plans to exclusively feed their baby mother's own milk up to 6 months,

• mother has/had an older child whom they successfully fed mother's own milk for a minimum of 6 months,

• mother is willing to participate in three 3-day study sessions and monthly measurement sessions, and

• mother provides informed consent for herself and her infant to participate.

Exclusion criteria: Mother-infant dyads are ineligible to participate if:

• the baby was born preterm (earlier than 37 weeks gestation),

• the baby was born outside the healthy weight range of 2,500 - 4,000 g (5lb 8oz to 8lb 13oz),

• the baby has a developmental delay diagnosed before the time of enrolment,

• the baby is currently receiving any medical treatment except for vitamin D supplementation (no more than 400 IU/day),

• the mother sought prescription medical treatment for lactation (e.g. domperidone, antibiotics, prescription nipple ointment), or

• the mother plans to move in the 6 months after starting the study.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	MAMA Lab, Mount Saint Vincent University	Halifax	Nova Scotia	Canada	B3M2J6

Sponsors and Collaborators

• Mount Saint Vincent University
• University of Prince Edward Island
• Queen's University

Investigators

• Principal Investigator: Kyly C Whitfield, PhD, Mount Saint Vincent University

Study Documents (Full-Text)

• Study Protocol and Informed Consent Form - Sep 27, 2019

More Information

Publications

None provided.

• Responsible Party: Mount Saint Vincent University
• ClinicalTrials.gov Identifier: NCT04041505
• Other Study ID Numbers: MSVUREB2018-155
• First Posted: Aug 1, 2019
• Last Update Posted: May 19, 2021
• Last Verified: May 1, 2021

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Mount Saint Vincent University: responsive feeding; expressing/pumping human milk

Study Results

No Results Posted as of May 19, 2021