A Randomised Controlled Trial to Compare Antenatal Preparation and Postnatal Counseling

National University Health System (NUHS)

Status: Completed

Conditions: Breastfeeding

Treatments: Behavioral: Lactation counseling

Study type: Interventional

Funder types: Other

Identifiers

NCT00270920

NHG RPR 03002

NUS IRB 03003

Details and patient eligibility

About

This is a randomised controlled trial to compare antenatal preparation and postnatal counseling strategies for improving breastfeeding rates.

The objectives are:

1. to study the effect of a standard two-encounter postnatal lactation counseling protocol on the initiation and maintenance of exclusive breastfeediing in mothers
2. to compare the effect of a standard two-encounter postnatal lactation counseling protocol with a single-encounter antenatal breastfeeding education protocol on the initiation and maintenance of exclusive breastfeeding in mothers.

Full description

All pregnant mothers who wish to breastfeed after 34 weeks of gestation, and who do not have a high risk pregnancy as determined by investigator or have a multiple pregnancy in current pregnancy and have given their written informed consent will be randomised into three groups. Group 1 will receive standard hospital care. Group 2 will receive 1 session of antenatal counseling and Group 3 will receive 2 sessions of postanatal lactation counseling. All will receive postnatal follow up phone calls using questions from Case Report Forms at 2 weeks, 8 weeks, 3 months, 6 months and 12 months. The mothers who are not contactable for 3 consecutive months will be withdrawn from the study.

Sex: Female

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Pregnant woman who wants to breastfeed her child after 34 weeks of gestation and written informed consent given

Exclusion criteria

Pregnant women with high risk pregnancy as determined by the investigator.