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Effect of boosting breastmilk supply on maternal and infant health

Not Applicable
Recruiting
Conditions
Obesity
Reproductive Health and Childbirth - Childbirth and postnatal care
Reproductive Health and Childbirth - Antenatal care
ow breastmilk production
Overweight
Diabetes Mellitus
Gestational diabetes mellitus
Polycystic Ovary Syndrome
Intrauterine Growth Restriction
Pre-eclampsia
Registration Number
ACTRN12621001250820
Lead Sponsor
The University of Western Australia - School of Molecular Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
180
Inclusion Criteria

To be eligible for the study participants must satisfy at least one or a combination of the following conditions.
- overweight defined by pre-pregnancy BMI 25 - 29.9
- obesity defined by pre-pregnancy BMI greater than or equal to 30
- pre-existing diabetes mellitus
- gestational diabetes mellitus (GDM)
- polycystic ovarian syndrome (PCOS)
- intrauterine growth restriction (IUGR)
- pregnancy induced hypertension
- preeclampsia
- previous history of low unexplained breastmilk supply

In addition participants must
- sign the RCT consent form
- be willing and able to comply with all study requirements, including intention to breastfeed for at least 6 months, timing and nature of required data collection and follow-up of mother and baby for 12 month period.

Exclusion Criteria

- preterm birth defined as births less than 37 completed weeks gestation
- infant syndromes or diseases that impact feeding
- previous breast surgery, including augmentation, reduction, breast lifts, nipple piercings and history of previous abscess requiring surgery/aspiration
- breast hypoplasia
- pituitary disorders
- contraindications to breastfeeding eg. HIV or mental health disorders where the participant is prescribed medication incompatible with breastfeeding
- multiple pregnancy (twins or more)
- non-English speaking women and those living outside the metropolitan area will not be recruited.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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