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Comparing Impacts of Donor Human Milk to Formula Supplementation on the Gut Microbiome of Full-term Infants (PPDHM)

Primary Purpose

Microbial Colonization

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Donor Human Milk - Nutritional Replacement
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Microbial Colonization focused on measuring Sleep, Microbiome, Growth, Postpartum depression, Maternal anger, Breastfeeding, Self-efficacy

Eligibility Criteria

37 Weeks - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Gestation greater than 37 weeks (full-term) Completion of antibiotic protocol for GBS during labour Vaginal delivery Intending on breastfeeding Consent for infant to receive DHM Working understanding (proficient in reading and understanding) English Mother has provided signed and dated informed consent and authorization to use protected health information, as required by national and local regulations. In the investigator's opinion, the subject mother understands and can comply with protocol requirements, instructions, and protocol-stated restrictions, and is likely to complete the study as planned. Exclusion Criteria: Diagnosed with clinically significant major congenital malformation that will interfere with breastfeeding or growth No intention to breastfeed Receiving extended courses of antibiotics (beyond that of the IAP in labour)

Sites / Locations

  • Rockyview General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Donor Human Milk

Standard Care (Infant Formula)

Arm Description

Infants randomized to the intervention group will receive DHM each time supplementation is required for the first 7 days of life.

Infants randomized to the standard care group will receive formula each time supplementation is required for the first 7 days of life.

Outcomes

Primary Outcome Measures

Infant gut microbiome - shallow shotgun metagenomics (RA)
Relative abundance
Infant gut microbiome - shallow shotgun metagenomics (RA)
Relative abundance
Infant gut microbiome - shallow shotgun metagenomics (RA)
Relative abundance
Infant gut microbiome - shallow shotgun metagenomics (alpha diversity)
alpha diversity of microbiome
Infant gut microbiome - shallow shotgun metagenomics (alpha diversity)
alpha diversity of microbiome
Infant gut microbiome - shallow shotgun metagenomics (alpha diversity)
alpha diversity of microbiome
Infant gut microbiome - shallow shotgun metagenomics (beta diversity)
beta diversity of microbiome
Infant gut microbiome - shallow shotgun metagenomics (beta diversity)
beta diversity of microbiome
Infant gut microbiome - shallow shotgun metagenomics (beta diversity)
beta diversity of microbiome

Secondary Outcome Measures

Infant Sleep
Brief Infant Sleep Questionnaire - Revised Short Form - Scores on each subscale and the total score are scaled from 0 to 100, with higher scores denoting better sleep quality, more positive perception of infant sleep, and parent behaviors that promote healthy and independent sleep.
Infant Sleep
Brief Infant Sleep Questionnaire- Scores on each subscale and the total score are scaled from 0 to 100, with higher scores denoting better sleep quality, more positive perception of infant sleep, and parent behaviors that promote healthy and independent sleep.
Infant Growth - weight
Weight - in grams; weight and height will be combined to report BMI in kg/m^2
Infant Growth - length
Length - in centimeters; weight and height will be combined to report BMI in kg/m^2
Infant Growth - BMI
Body mass index - weight and height will be combined to report BMI in kg/m^2
Infant Growth - BMI
Body mass index - weight and height will be combined to report BMI in kg/m^2
Infant Growth - BMI
Body mass index - weight and height will be combined to report BMI in kg/m^2
Infant Growth - head
Head circumference - in centimeters
Infant Growth - weight
Weight- in grams; weight and height will be combined to report BMI in kg/m^2
Infant Growth- length
Length - in centimeters; weight and height will be combined to report BMI in kg/m^2
Infant Growth - head
Head circumference - in centimeters
Infant Growth - weight
Weight- in grams; weight and height will be combined to report BMI in kg/m^2
Infant Growth- length
Length - in centimeters; weight and height will be combined to report BMI in kg/m^2
Infant Growth - head
Head circumference - in centimeters
Infant feeding
breastfeeding exclusivity - measured by 7-day infant feeding journal. Number of participants whose consume only breastmilk.
Infant feeding
breastfeeding exclusivity - measured by 7-day maternal recall. Number of participants whose consume only breastmilk.
Infant feeding
breastfeeding exclusivity- measured by 7-day maternal recall. Number of participants whose consume only breastmilk.
Maternal Depression
Edinburgh Postnatal Depression Screen - Range in score from 0 to 30; higher scores indicate worse outcomes
Maternal Depression
Edinburgh Postnatal Depression Screen - Range in score from 0 to 30; higher scores indicate worse outcomes
Maternal Depression
Edinburgh Postnatal Depression Screen -- Range in score from 0 to 30; higher scores indicate worse outcomes
Maternal Anger
LEVEL 2-Anger-Adult (PROMIS Emotional Distress-Anger- Short Form): Range in score from 5 to 25 with higher scores indicating greater severity of anger.
Maternal Anger
LEVEL 2-Anger-Adult (PROMIS Emotional Distress-Anger- Short Form): Range in score from 5 to 25 with higher scores indicating greater severity of anger.
Maternal Anger
LEVEL 2-Anger-Adult (PROMIS Emotional Distress-Anger- Short Form): Range in score from 5 to 25 with higher scores indicating greater severity of anger.
Maternal Breastfeeding Self-efficacy
Breastfeeding self-efficacy scale - short form: Total scores range from 14 to 70, with higher scores reflecting more significant levels of breastfeeding self-efficacy.
Maternal Breastfeeding Self-efficacy
Breastfeeding self-efficacy scale - short form: Total scores range from 14 to 70, with higher scores reflecting more significant levels of breastfeeding self-efficacy.
Maternal Breastfeeding Self-efficacy
Breastfeeding self-efficacy scale - short form: Total scores range from 14 to 70, with higher scores reflecting more significant levels of breastfeeding self-efficacy.
Maternal Anxiety
State - trait Anxiety inventory: Total scores range from 20 to 80 (each for state and trait), with higher scores indicating worse outcomes (higher anxiety).
Maternal Anxiety
State Anxiety inventory: Total scores range from 20 to 80, with higher scores indicating worse outcomes (higher anxiety).
Maternal Anxiety
State Anxiety inventory: Total scores range from 20 to 80, with higher scores indicating worse outcomes (higher anxiety).

Full Information

First Posted
March 15, 2023
Last Updated
July 1, 2023
Sponsor
University of Calgary
Collaborators
University of British Columbia, University of Victoria, NorthernStar Mothers Milk Bank
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1. Study Identification

Unique Protocol Identification Number
NCT05815433
Brief Title
Comparing Impacts of Donor Human Milk to Formula Supplementation on the Gut Microbiome of Full-term Infants
Acronym
PPDHM
Official Title
Comparing Impacts of Donor Human Milk to Formula Supplementation on the Gut Microbiome of Full-term Infants Exposed to Antibiotics in Labour: A Pilot Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2023 (Actual)
Primary Completion Date
March 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary
Collaborators
University of British Columbia, University of Victoria, NorthernStar Mothers Milk Bank

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 goal of this pilot randomized controlled trial (RCT) is to examine donor human milk (DHM) as a clinical intervention targeted at achieving beneficial microbiome signatures in full-term infants who are exposed to intrapartum antibiotic prophylaxis (IAP) therapy during labour. Secondarily, this study aims to compare the infant health outcomes of sleep and growth between groups to assess if these outcomes are mediated by infant feeding type or potential differences in microbial signatures. Finally, this study will compare maternal outcomes of depression, anger, breastfeeding self-efficacy and breastfeeding rates between groups. The hypothesis of this study is: that replacing formula with DHM supplementation will minimize gut microbiome dysbiosis and foster homeostasis following supplementation. In addition, it is hypothesized that improved homeostasis will promote improved sleep and growth outcomes in participant infants. Finally, mothers whose infants receive DHM will have lower depression and anger scores and high breastfeeding self-efficacy and exclusive breastfeeding rates compared to mothers whose infants receive formula.
Detailed Description
Investigators propose to conduct a pilot clinical RCT in the postpartum hospital setting examining DHM as an intervention provided to full-term infants who are exposed to Group B Streptococcus (GBS) antibiotic prophylaxis during labour. Randomization of participant infants is currently an ethical practice because DHM supplementation is not standard practice in this population; infants receive formula if supplementation of mother's own milk (MOM) is required. Additionally, randomization will allow investigators to determine causal relationships between DHM supplementation compared to formula supplementation on the infant gut microbiome. Finally, conducting research in the clinical setting will allow for pragmatic assessment of DHM as an intervention, enhancing external validity and increasing the likelihood of its implementation into healthcare systems to improve healthcare quality. Population: The population of interest is vaginally born, full-term infants who are exposed to antibiotics in labour through IAP and whose mothers are planning on breastfeeding. Recruitment: Mothers greater than 37 weeks' gestation admitted to the postpartum unit who test positive for GBS and deliver vaginally will be screened for participation in the study by nurses on the postpartum unit. Approximately 20% of all pregnant mothers will test positive for GBS and Alberta Health Services protocol indicates that GBS-positive mothers are given intravenous antibiotics during labour. Only mothers who receive the complete Alberta Health Services protocol will qualify for the study. Upon recruitment and completion of informed consent, infants requiring supplementation of MOM will be randomized to the control or intervention group. Investigators will randomize 60 mother-infant dyads, providing adequate power to detect overall microbiome differences (~30 in each group). Intervention - Donor Human Milk (DHM): Infants randomized to the intervention group will receive DHM each time supplementation is required for the first 7 days of life. The exposure time of 7 days was selected due to feasibility of DHM cost, and this is the period when breastfeeding is being established and most formula supplementation occurs. Infants in the control group will receive formula when supplementation is required (standard care). All DHM in North America is pasteurized and provided through certified milk banks regulated by the Human Milk Banking Association of North America and DHM for this study will be obtained from the NorthernStar Mothers Milk Bank (NMMB). Data Collection, Analysis, and Outcomes: The primary outcome for this pilot study will result from comparisons of DHM to formula supplementation groups for differences in microbiome signatures, such as diversity, proportions of Bifidobacteria, and proportions of pathogenic organisms. Infant stool samples will be collected from soiled diapers at one, six and 12 weeks postpartum. Secondary outcomes include infant growth, sleep, and breastfeeding outcomes that will be collected at one, six and 12 weeks postpartum.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Microbial Colonization
Keywords
Sleep, Microbiome, Growth, Postpartum depression, Maternal anger, Breastfeeding, Self-efficacy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
An experimental study design in which each participants will be randomized to one of two groups (intervention [DHM] or standard care/control [formula])
Masking
Outcomes Assessor
Masking Description
Assessors who are conducting the microbial analysis and statistical analysis will not be aware of which group is intervention and which is control. These groups will be assigned a number (Group 1; Group 2).
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Donor Human Milk
Arm Type
Experimental
Arm Description
Infants randomized to the intervention group will receive DHM each time supplementation is required for the first 7 days of life.
Arm Title
Standard Care (Infant Formula)
Arm Type
No Intervention
Arm Description
Infants randomized to the standard care group will receive formula each time supplementation is required for the first 7 days of life.
Intervention Type
Other
Intervention Name(s)
Donor Human Milk - Nutritional Replacement
Intervention Description
All DHM in North America is pasteurized and provided through certified milk banks regulated by the Human Milk Banking Association of North America. DHM for this study will be obtained from the NorthernStar Mothers Milk Bank (NMMB). The milk is pasteurized and rigorously tested according to Human Milk Banking of North America guidelines. In Canada, DHM is categorized as food or nutritional therapy and the milk bank is monitored and certified by the Canadian Food Inspection Agency. The product used for this study will be the same product that is provided to other hospital units (mainly the neonatal intensive care units) in Alberta and around Canada. The product will not be modified or tampered with in any way.
Primary Outcome Measure Information:
Title
Infant gut microbiome - shallow shotgun metagenomics (RA)
Description
Relative abundance
Time Frame
one week postpartum
Title
Infant gut microbiome - shallow shotgun metagenomics (RA)
Description
Relative abundance
Time Frame
six weeks postpartum
Title
Infant gut microbiome - shallow shotgun metagenomics (RA)
Description
Relative abundance
Time Frame
twelve weeks postpartum
Title
Infant gut microbiome - shallow shotgun metagenomics (alpha diversity)
Description
alpha diversity of microbiome
Time Frame
one week postpartum
Title
Infant gut microbiome - shallow shotgun metagenomics (alpha diversity)
Description
alpha diversity of microbiome
Time Frame
six weeks postpartum
Title
Infant gut microbiome - shallow shotgun metagenomics (alpha diversity)
Description
alpha diversity of microbiome
Time Frame
twelve weeks postpartum
Title
Infant gut microbiome - shallow shotgun metagenomics (beta diversity)
Description
beta diversity of microbiome
Time Frame
one week postpartum
Title
Infant gut microbiome - shallow shotgun metagenomics (beta diversity)
Description
beta diversity of microbiome
Time Frame
six weeks postpartum
Title
Infant gut microbiome - shallow shotgun metagenomics (beta diversity)
Description
beta diversity of microbiome
Time Frame
twelve weeks postpartum
Secondary Outcome Measure Information:
Title
Infant Sleep
Description
Brief Infant Sleep Questionnaire - Revised Short Form - Scores on each subscale and the total score are scaled from 0 to 100, with higher scores denoting better sleep quality, more positive perception of infant sleep, and parent behaviors that promote healthy and independent sleep.
Time Frame
Six weeks postpartum
Title
Infant Sleep
Description
Brief Infant Sleep Questionnaire- Scores on each subscale and the total score are scaled from 0 to 100, with higher scores denoting better sleep quality, more positive perception of infant sleep, and parent behaviors that promote healthy and independent sleep.
Time Frame
Twelve weeks postpartum
Title
Infant Growth - weight
Description
Weight - in grams; weight and height will be combined to report BMI in kg/m^2
Time Frame
one week postpartum
Title
Infant Growth - length
Description
Length - in centimeters; weight and height will be combined to report BMI in kg/m^2
Time Frame
one week postpartum
Title
Infant Growth - BMI
Description
Body mass index - weight and height will be combined to report BMI in kg/m^2
Time Frame
one week postpartum
Title
Infant Growth - BMI
Description
Body mass index - weight and height will be combined to report BMI in kg/m^2
Time Frame
six weeks postpartum
Title
Infant Growth - BMI
Description
Body mass index - weight and height will be combined to report BMI in kg/m^2
Time Frame
twelve weeks postpartum
Title
Infant Growth - head
Description
Head circumference - in centimeters
Time Frame
one week postpartum
Title
Infant Growth - weight
Description
Weight- in grams; weight and height will be combined to report BMI in kg/m^2
Time Frame
six weeks postpartum
Title
Infant Growth- length
Description
Length - in centimeters; weight and height will be combined to report BMI in kg/m^2
Time Frame
six weeks postpartum
Title
Infant Growth - head
Description
Head circumference - in centimeters
Time Frame
six weeks postpartum
Title
Infant Growth - weight
Description
Weight- in grams; weight and height will be combined to report BMI in kg/m^2
Time Frame
Twelve weeks postpartum
Title
Infant Growth- length
Description
Length - in centimeters; weight and height will be combined to report BMI in kg/m^2
Time Frame
Twelve weeks postpartum
Title
Infant Growth - head
Description
Head circumference - in centimeters
Time Frame
Twelve weeks postpartum
Title
Infant feeding
Description
breastfeeding exclusivity - measured by 7-day infant feeding journal. Number of participants whose consume only breastmilk.
Time Frame
one week postpartum
Title
Infant feeding
Description
breastfeeding exclusivity - measured by 7-day maternal recall. Number of participants whose consume only breastmilk.
Time Frame
six weeks postpartum
Title
Infant feeding
Description
breastfeeding exclusivity- measured by 7-day maternal recall. Number of participants whose consume only breastmilk.
Time Frame
twelve weeks postpartum
Title
Maternal Depression
Description
Edinburgh Postnatal Depression Screen - Range in score from 0 to 30; higher scores indicate worse outcomes
Time Frame
one week postpartum
Title
Maternal Depression
Description
Edinburgh Postnatal Depression Screen - Range in score from 0 to 30; higher scores indicate worse outcomes
Time Frame
six weeks postpartum
Title
Maternal Depression
Description
Edinburgh Postnatal Depression Screen -- Range in score from 0 to 30; higher scores indicate worse outcomes
Time Frame
twelve weeks postpartum
Title
Maternal Anger
Description
LEVEL 2-Anger-Adult (PROMIS Emotional Distress-Anger- Short Form): Range in score from 5 to 25 with higher scores indicating greater severity of anger.
Time Frame
one week postpartum
Title
Maternal Anger
Description
LEVEL 2-Anger-Adult (PROMIS Emotional Distress-Anger- Short Form): Range in score from 5 to 25 with higher scores indicating greater severity of anger.
Time Frame
six weeks postpartum
Title
Maternal Anger
Description
LEVEL 2-Anger-Adult (PROMIS Emotional Distress-Anger- Short Form): Range in score from 5 to 25 with higher scores indicating greater severity of anger.
Time Frame
twelve weeks postpartum
Title
Maternal Breastfeeding Self-efficacy
Description
Breastfeeding self-efficacy scale - short form: Total scores range from 14 to 70, with higher scores reflecting more significant levels of breastfeeding self-efficacy.
Time Frame
one week postpartum
Title
Maternal Breastfeeding Self-efficacy
Description
Breastfeeding self-efficacy scale - short form: Total scores range from 14 to 70, with higher scores reflecting more significant levels of breastfeeding self-efficacy.
Time Frame
six weeks postpartum
Title
Maternal Breastfeeding Self-efficacy
Description
Breastfeeding self-efficacy scale - short form: Total scores range from 14 to 70, with higher scores reflecting more significant levels of breastfeeding self-efficacy.
Time Frame
twelve weeks postpartum
Title
Maternal Anxiety
Description
State - trait Anxiety inventory: Total scores range from 20 to 80 (each for state and trait), with higher scores indicating worse outcomes (higher anxiety).
Time Frame
Baseline - (birth/enrolment)
Title
Maternal Anxiety
Description
State Anxiety inventory: Total scores range from 20 to 80, with higher scores indicating worse outcomes (higher anxiety).
Time Frame
six weeks postpartum
Title
Maternal Anxiety
Description
State Anxiety inventory: Total scores range from 20 to 80, with higher scores indicating worse outcomes (higher anxiety).
Time Frame
twelve weeks postpartum

10. Eligibility

Sex
All
Minimum Age & Unit of Time
37 Weeks
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Gestation greater than 37 weeks (full-term) Completion of antibiotic protocol for GBS during labour Vaginal delivery Intending on breastfeeding Consent for infant to receive DHM Working understanding (proficient in reading and understanding) English Mother has provided signed and dated informed consent and authorization to use protected health information, as required by national and local regulations. In the investigator's opinion, the subject mother understands and can comply with protocol requirements, instructions, and protocol-stated restrictions, and is likely to complete the study as planned. Exclusion Criteria: Diagnosed with clinically significant major congenital malformation that will interfere with breastfeeding or growth No intention to breastfeed Receiving extended courses of antibiotics (beyond that of the IAP in labour)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Meredith Brockway, PhD
Phone
4036890970
Email
mbrockwa@ucalgary.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Jannette Festival, BN
Phone
403-475-6455
Email
director@northernstarmilkbank.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Meredith Brockway, PhD RN
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rockyview General Hospital
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2V 1P9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dena Berci, MN
Phone
(403) 943-3109
Email
dena.berci@albertahealthservices.ca
Ext
Brockway
Email
mbrockwa@ucalgary.ca
First Name & Middle Initial & Last Name & Degree
Meredith Brockway, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data will be shared upon request
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Comparing Impacts of Donor Human Milk to Formula Supplementation on the Gut Microbiome of Full-term Infants

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