Effect of boosting breastmilk supply on maternal and infant health
- Conditions
- ObesityReproductive Health and Childbirth - Childbirth and postnatal careReproductive Health and Childbirth - Antenatal careow breastmilk productionOverweightDiabetes MellitusGestational diabetes mellitusPolycystic Ovary SyndromeIntrauterine Growth RestrictionPre-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
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.
- 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
Name Time Method
- Secondary Outcome Measures
Name Time Method