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A Randomized Controlled Trial of an Antenatal Intervention to Increase Exclusive Breastfeeding

A Randomized Controlled Trial of an Antenatal Intervention to Increase Exclusive Breastfeeding

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01648114
Acronym
ABFS
Enrollment
472
Registered
2012-07-24
Start date
2012-08-31
Completion date
2014-02-28
Last updated
2015-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding, Pregnancy

Keywords

breastfeeding, pregnancy, antenatal, exclusive breastfeeding, education

Brief summary

The investigators will conduct an educational intervention for pregnant women who are planning to breastfeed to promote exclusive breastfeeding and to increase the duration of breastfeeding.

Detailed description

The intervention will include a 20 to 30-minute one-to-one educational talk by a lactation expert explaining the facts of breastfeeding and answering participant questions. The educational intervention will focus on: (1) the importance of exclusive breastfeeding, (2) milk supply/demand and feeding on demand, (3) frequency of feedings, feeding cues, how to know an infant is getting enough milk, (4) avoiding artificial nipples until the infant is nursing well, (5) the importance of a good latch, (5) where to seek breastfeeding help and support, and (7) returning to work and continuing breastfeeding.

Interventions

OTHERAntenatal Breastfeeding Intervention

The intervention will include a 20 to 30-minute one-to-one educational talk by a lactation expert explaining the facts of breastfeeding and answering participant questions. The educational intervention will focus on: (1) the importance of exclusive breastfeeding, (2) milk supply/demand and feeding on demand, (3) frequency of feedings, feeding cues, how to know an infant is getting enough milk, (4) avoiding artificial nipples until the infant is nursing well, (5) the importance of a good latch, (5) where to seek breastfeeding help and support, and (7) returning to work and continuing breastfeeding

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. singleton pregnancy, 2. primiparous 3. 18 years of age or older, 4. at least 36 weeks of gestation, 5. Cantonese speaking, 6. Hong Kong resident, 7. no serious medical or obstetrical complications, 8. staying in Hong Kong for at least 6 months after delivery, and 9. intention to breastfeed.

Exclusion criteria

Participants will be excluded from the study if they are not entitled to health benefits in Hong Kong (NEP).

Design outcomes

Primary

MeasureTime frameDescription
Exclusive Breastfeeding Rate6 weeks postpartumExclusive breastfeeding rate at 6 weeks postpartum

Secondary

MeasureTime frameDescription
Median Duration of Breastfeeding6 months postpartumThe median duration of exclusive breastfeeding and the median duration of any breastfeeding
Exclusive Breastfeeding Rate at 3 Months and 6 Months Postpartum6 Months PostpartumRate of Exclusive Breastfeeding at 3 Months and 6 Months Postpartum

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026