Skip to content

Professional Breastfeeding Support Intervention

A Randomized Controlled Trial of a Professional Breastfeeding Support Intervention to Increase the Exclusivity and Duration of Breastfeeding

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01893736
Enrollment
722
Registered
2013-07-09
Start date
2010-09-30
Completion date
2013-03-31
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

Keywords

Breastfeeding, professional support, postnatal, interventions, exclusive breastfeeding, randomized controlled trial

Brief summary

The investigators will conduct an early postpartum professional breastfeeding intervention to postpartum women who are intended to breastfeed newborn babies to improve breastfeeding outcomes.

Detailed description

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.

Interventions

OTHERIn-hospital professional support

In-hospital professional lactation support will consist of two 30-minute one-to-one hands-on breastfeeding counseling sessions in first 24 hours post-partum and one further 30-minute one-to-one hands-on breastfeeding counseling session on the second day of post-partum hospitalization for a total of three 30-minute sessions. The one-to-one sessions will focus on: (1) education and advice on correct breastfeeding positions and techniques, (2) education and advice on milk supply and how to avoid common breastfeeding problems, and (3) hands-on instruction and assistance with proper breastfeeding positioning and technique, latching on and newborn attachment to the breast, and manual expression of breast milk.

OTHERPostpartum telephone follow-up support

Postpartum telephone follow-up support will consist of telephone support 72 hours after hospital discharge and weekly for the first 4 weeks, or until weaned. Earlier telephone contacts will focus more on breastfeeding topics. Information will be solicited from the participants about problems or difficulties they are experiencing. Supportive advice will be provided regarding management of breastfeeding problems, and support and encouragement for the continuation of breastfeeding. Later contacts will focus more on advice and encouragement on breastfeeding while resuming daily activities or returning to work, nursing in public places, and expressing and storing breast milk.

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. delivers at participating trial site, 2. primiparous, 3. intends to breastfeed, 4. 18 years of age or older, 5. has singleton pregnancy, 6. Cantonese speaking, 7. Hong Kong resident for more than one year, 8. no serious medical or obstetrical complications

Exclusion criteria

1. \< 37 weeks gestation, 2. an Apgar score \< 8 at five minutes, 3. a birth weight \< 2500 grams, 4. born with any severe medical conditions or congenital malformations, 5. is placed in the special care nursery for more than 48 hours after delivery, 6. is placed in the intensive care nursery after delivery, 7. not entitled to health benefits in Hong Kong (NEP).

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of any and exclusive breastfeeding1 month postpartumAny breastfeeding rate and exclusive breastfeeding rate at 1 month postpartum

Secondary

MeasureTime frameDescription
Median duration of breastfeeding6 month postpartumThe median duration of any breastfeeding and the median duration of exclusive breastfeeding.

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026