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Does post-natal breastfeeding support improve rates of breastfeeding?

Randomized, controlled trial of a postnatal lactation consultant intervention on duration of breastfeeding up to 6 months

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618001225202
Enrollment
765
Registered
2018-07-20
Start date
2018-02-26
Completion date
2019-09-19
Last updated
2020-12-07

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

Conditions

None listed

Brief summary

Despite awareness of the advantages of breastfeeding, the rates often fall short of expected practice. In the Whittlesea area alone, the initial rate of breastfeeding is very high at >94% of newborn infants. However, rates drop by 30% at 8 weeks (2 months) post-birth. At The Northern Hospital, there are 2 support systems in place. This is in line with UNICEF and the World Health Organization (WHO) breastfeeding practices. First, all expecting mothers are invited to attend breastfeeding seminars prior to the delivery of their newborns. Secondly, TNH also has a breastfeeding clinic that runs daily and mothers can refer themselves to this clinic when and if they feel the need. However, there is a perception that once the mothers leave hospital, there is lack of breastfeeding support, so we feel that we need to do more to help promote breastfeeding. Our hypothesis was that breastfeeding rates can be improved with additional support and education from a lactation consultant. The study aims to determine if additional support for breastfeeding mothers after they leave hospital improves rates of breastfeeding. In this randomized controlled trial, participants will be randomized to either an intervention or a control group. In the intervention group, a LACTATION CONSULTANT will provide active communication and assistance via telephone to breastfeeding mothers, especially during the first 4 weeks after discharge and then again after 3 months and 6 months. In the control group, a LACTATION CONSULTANT will contact breastfeeding mothers via telephone after 1 month, 3 months, and 6 months to ask about breastfeeding activity/practices. At the end of the study, we will compare the rates of breastfeeding in mothers who received the intervention compared to the control group and determine whether additional assistance from lactation consultants is associated with longer breastfeeding duration.

Interventions

INTERVENTION: Lactation Consultant (LC) Services -Participants assigned to this group will receive special intervention in addition to the standard of care. -A lactation consultant will visit them to introduce herself prior to discharge from the postnatal ward. -They will receive regular phone/text communication from the lactation consultant, especially during the early period within 4 weeks of giving birth -A lactation consultant with minimum 10 years experience will conduct all phone calls

INTERVENTION: Lactation Consultant (LC) Services -Participants assigned to this group will receive special intervention in addition to the standard of care. -A lactation consultant will visit them to introduce herself prior to discharge from the postnatal ward. -They will receive regular phone/text communication from the lactation consultant, especially during the early period within 4 weeks of giving birth -A lactation consultant with minimum 10 years experience will conduct all phone calls to recruited individuals -Communications with the lactation consultant will seek to identify and solve breastfeeding difficulties, with referral of mothers to the breastfeeding clinic if required. -Subjects will also be asked to report on their breastfeeding progress (ie whether they have continued to exclusively breastfeeding, are now hybrid breastfeeding, or have switched to formula feeding). -Contact will be made over the phone at post-natal dates: 1 week, 2 weeks, 3 weeks, 4 weeks, 3 months, and 6 months -Participants who can not be reached by phone the first time will be left a voicemail, sent a text message, and follow-up calls will be an additional two times that week before they are classified as 'lost to follow-up'

Sponsors

Professor Wei Qi Fan
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Healthy volunteers
Yes

Inclusion criteria

Participants must: • be breastfeeding or intending to breastfeed at discharge • have no illness that would make breastfeeding success difficult • baby is more than 36 weeks gestation at the time of delivery • be able to communicate in English.

Exclusion criteria

-Current maternal treatment with medications that are contraindicated with breastfeeding

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026