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Breastfeed a Better Youngster: the BABY Study (BABY)

Primary Purpose

Breastfeeding, Breastfeeding, Exclusive, Infant Behavior

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Relaxation meditation tape
Sponsored by
University College, London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breastfeeding focused on measuring breastfeeding, maternal stress, infant behavior, infant development, relaxation

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Primiparous mother with singleton pregnancy who is breastfeeding her late preterm infants
  • Infant is singleton born at 34 0/7-37 6/7 weeks of gestation.
  • Mother and infant are generally healthy (free of serious diseases that can affect breastfeeding or nursing infant, or energy balance of the infant).
  • No current involvement in other research studies that can potentially affect any of outcome measures.

Exclusion Criteria:

  • Infant with serious underlying or chronic disease*
  • Mothers who smoke
  • Infant receiving any medication regularly

Sites / Locations

  • Beijing Children Hospital
  • Zhuang Wei

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

relaxation meditation tape

Normal care

Arm Description

Participants in this arm will be asked to use the relaxation therapy during the feed at least once a day. Participants will be given a diary to record when it is used. Participants will be encouraged to use the tape as often as they find it helpful.

Participants in this arm will receive normal care from the Beijing Children Hospital

Outcomes

Primary Outcome Measures

Changes in maternal stress from baseline to 8 weeks postpartum
Measurement for maternal stress will use the Cohen's Perceived Stress Scale (PSS). The PSS is a 14-item psychological self-rating scale for measuring the perception of stress on a scale of five, from 0 (never) to 4 (very often).

Secondary Outcome Measures

Infant weight
Infant weight will be measured at baseline and the 8-week home visit (unit kg)
Infant length
Infant length will be measured at baseline and the 8-week home visit (unit cm)
Infant head circumference
Infant head circumference will be measured at baseline and the 8-week home visit (unit cm)
Infant temperament
Measured using the revised Rothbart Infant Behaviour Questionnaire (RIBQ) at 2 months of age. The RIBQ is a 7-point Likert scale, from 1 (never) to 7 (always). Three major dimensions will be used for the assessment of infant temperament; surgency/extraversion, negative affectivity and orienting/regulation.
Infant behaviour
Measured by 3-day infant behaviour diary (average mins per day spent in each behavioural state). The diary consists of a time scale for 72 hours, which is divided into 15 minutes segments, and has five categories of behaviour: Sleeping, Awake and content, Fussy, Crying and Feeding.
Infant appetite
Measured using the Baby Eating Behaviour Questionnaire (BEBQ) at 2 months of age. It consists of 18 items designed to measure four traits: "enjoyment of food" (4 items), "food responsiveness" (5 items), "slowness in eating" (4 items), and satiety responsiveness" (5 items). The mothers in this study will be asked to rate all items based on a scale from 1 (never) to 5 (always).
Composition of milk macronutrients (fat, protein, carbohydrate)
Measured by Mid-infrared milk analyser (unit is g/100ml)
Composition of microbiota in breastmilk samples at one week and 8-week postpartum
Measured using the 16S rRNA based amplicon sequencing technique
Composition of microbiota in stool samples at one week and 8-week postpartum
Measured using the 16S rRNA based amplicon sequencing technique
Breast milk volume at 8 weeks
The milk volume will be measured using the test-weighing method.
Energy content of the milk
The energy content will estimated from the milk volume measurement provided by Mid-infrared milk analyser in ml and kcal/100ml

Full Information

First Posted
August 29, 2018
Last Updated
November 3, 2020
Sponsor
University College, London
Collaborators
Beijing Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03674632
Brief Title
Breastfeed a Better Youngster: the BABY Study
Acronym
BABY
Official Title
Mother-infant Signalling During Lactation Following Late Preterm and Early Term Delivery: An Investigation of Physiological, Psychological and Anthropological Factors
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
November 25, 2018 (Actual)
Primary Completion Date
October 31, 2020 (Actual)
Study Completion Date
October 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University College, London
Collaborators
Beijing Children's Hospital

4. Oversight

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

5. Study Description

Brief Summary
This research will investigate different aspects of the 'signalling' between mother and infant during breastfeeding in a stressful situation following late preterm and early term delivery, when breastfeeding is often challenging. The researcher will conduct a single-blinded randomised controlled trial in Chinese mothers who deliver a late preterm infant (LPI; 34 0/7-36 6/7 weeks of gestation) and mothers who deliver a early term infant (ETI; 37 0/7-37 6/7) and plan to exclusively breast-feed.This study will investigate the role of the milk and infant gut microbiome as a potential 'signal' in this process. A relaxation intervention (meditation tape) will be used to reduce stress levels in mothers who are expressing breast-milk or breastfeeding their infant (born at 34 0/7-37 6/7 weeks completed gestation). This study will investigate whether lower levels of stress in the mother result in more successful and effective breastfeeding, leading to improved infant outcomes (better growth, longer sleep duration and reduced crying).
Detailed Description
Participants will be recruited while they are in the maternity hospital. A baseline assessment will be conducted during the 1-week postpartum home visit, with another study visit at 8 weeks after delivery. After obtaining written informed consent, subjects will be randomly assigned to either the intervention arm or control conditions (standard management). Participants will be told that the aim of the study is to investigate factors that may make breastfeeding easier for mothers with a LPI and ETI, so they can breast-feed for longer. They will not be told about the randomisation until the end of the study, as this knowledge would most likely lead to mothers in the control group using some form of relaxation therapy. Background characteristics of mothers and their early feeding experiences will be recorded. Participants can choose to complete the questionnaires on paper or online in their own time after the study visit. A breast milk sample will be collected pre-feed and infant anthropometry will be assessed by a trained nurse pre-feed at each home visit. Feed duration will be noted by the trained nurse. Stool samples of infants who were born vaginally will be collected by a trained nurse at baseline and at 8-weeks. At 3-month and 6-month postpartum, there will be a telephone contact to the participants for follow-up. Participants will be invited to complete the infant questionnaires again on paper or online in their own time.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breastfeeding, Breastfeeding, Exclusive, Infant Behavior, Psychological Stress, Breast Milk Expression, Infant Development
Keywords
breastfeeding, maternal stress, infant behavior, infant development, relaxation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
96 (Actual)

8. Arms, Groups, and Interventions

Arm Title
relaxation meditation tape
Arm Type
Experimental
Arm Description
Participants in this arm will be asked to use the relaxation therapy during the feed at least once a day. Participants will be given a diary to record when it is used. Participants will be encouraged to use the tape as often as they find it helpful.
Arm Title
Normal care
Arm Type
No Intervention
Arm Description
Participants in this arm will receive normal care from the Beijing Children Hospital
Intervention Type
Behavioral
Intervention Name(s)
Relaxation meditation tape
Intervention Description
The tape used in this study is based on a meditation CD designed for breastfeeding mother (Menelli, 2004). The recording will be transcribed and translated into Chinese language by a certified yoga therapist.
Primary Outcome Measure Information:
Title
Changes in maternal stress from baseline to 8 weeks postpartum
Description
Measurement for maternal stress will use the Cohen's Perceived Stress Scale (PSS). The PSS is a 14-item psychological self-rating scale for measuring the perception of stress on a scale of five, from 0 (never) to 4 (very often).
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Infant weight
Description
Infant weight will be measured at baseline and the 8-week home visit (unit kg)
Time Frame
8 weeks
Title
Infant length
Description
Infant length will be measured at baseline and the 8-week home visit (unit cm)
Time Frame
8 weeks
Title
Infant head circumference
Description
Infant head circumference will be measured at baseline and the 8-week home visit (unit cm)
Time Frame
8 weeks
Title
Infant temperament
Description
Measured using the revised Rothbart Infant Behaviour Questionnaire (RIBQ) at 2 months of age. The RIBQ is a 7-point Likert scale, from 1 (never) to 7 (always). Three major dimensions will be used for the assessment of infant temperament; surgency/extraversion, negative affectivity and orienting/regulation.
Time Frame
8 weeks
Title
Infant behaviour
Description
Measured by 3-day infant behaviour diary (average mins per day spent in each behavioural state). The diary consists of a time scale for 72 hours, which is divided into 15 minutes segments, and has five categories of behaviour: Sleeping, Awake and content, Fussy, Crying and Feeding.
Time Frame
8 weeks
Title
Infant appetite
Description
Measured using the Baby Eating Behaviour Questionnaire (BEBQ) at 2 months of age. It consists of 18 items designed to measure four traits: "enjoyment of food" (4 items), "food responsiveness" (5 items), "slowness in eating" (4 items), and satiety responsiveness" (5 items). The mothers in this study will be asked to rate all items based on a scale from 1 (never) to 5 (always).
Time Frame
8 weeks
Title
Composition of milk macronutrients (fat, protein, carbohydrate)
Description
Measured by Mid-infrared milk analyser (unit is g/100ml)
Time Frame
10 minutes
Title
Composition of microbiota in breastmilk samples at one week and 8-week postpartum
Description
Measured using the 16S rRNA based amplicon sequencing technique
Time Frame
8 weeks
Title
Composition of microbiota in stool samples at one week and 8-week postpartum
Description
Measured using the 16S rRNA based amplicon sequencing technique
Time Frame
8 weeks
Title
Breast milk volume at 8 weeks
Description
The milk volume will be measured using the test-weighing method.
Time Frame
8 weeks
Title
Energy content of the milk
Description
The energy content will estimated from the milk volume measurement provided by Mid-infrared milk analyser in ml and kcal/100ml
Time Frame
10 minutes

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Primiparous mother with singleton pregnancy who is breastfeeding her late preterm infants Infant is singleton born at 34 0/7-37 6/7 weeks of gestation. Mother and infant are generally healthy (free of serious diseases that can affect breastfeeding or nursing infant, or energy balance of the infant). No current involvement in other research studies that can potentially affect any of outcome measures. Exclusion Criteria: Infant with serious underlying or chronic disease* Mothers who smoke Infant receiving any medication regularly
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mary Fewtrell, PhD
Organizational Affiliation
University College, London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing Children Hospital
City
Beijing
ZIP/Postal Code
100045
Country
China
Facility Name
Zhuang Wei
City
Beijing
ZIP/Postal Code
100192
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The IPD will only be used in a PhD thesis and further investigations
Citations:
PubMed Identifier
31889973
Citation
Yu J, Wells J, Wei Z, Fewtrell M. Effects of relaxation therapy on maternal psychological state, infant growth and gut microbiome: protocol for a randomised controlled trial investigating mother-infant signalling during lactation following late preterm and early term delivery. Int Breastfeed J. 2019 Dec 16;14:50. doi: 10.1186/s13006-019-0246-5. eCollection 2019.
Results Reference
derived

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Breastfeed a Better Youngster: the BABY Study

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