Breastfeeding Clinical Trial
Official title:
A Randomized Controlled Trial of a Professional Breastfeeding Support Intervention to Increase the Exclusivity and Duration of Breastfeeding
The investigators will conduct an early postpartum professional breastfeeding intervention to postpartum women who are intended to breastfeed newborn babies to improve breastfeeding outcomes.
The aim of this study is to determine whether early post-partum professional breastfeeding
support improves breastfeeding outcomes.
The primary hypotheses are:
1. Exclusive breastfeeding rates at 1, 2, and 3 months will be increased among
mother-infant pairs who receive professional lactation support or telephone follow-up
support (intervention groups) when compared with those who receive usual post-natal
breastfeeding support (control group);
2. The rate of any breastfeeding (predominant or partial) at 1, 2, and 3 months will be
increased among mother-infant pairs in the intervention groups when compared with those
in the control group;
The secondary hypotheses are:
1. The overall duration of exclusive breastfeeding will be increased among mother-infant
pairs in the intervention groups when compared with those in the control group;
2. The overall duration of any breastfeeding (predominant or partial) will be increased
among mother-infant pairs in the intervention groups when compared with those in the
control group.
;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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