None listed
Conditions
Brief summary
The Victorian Government’s commitment to improving breastfeeding rates includes the development of the Victorian Breastfeeding Action Plan. The Victorian Breastfeeding Research Project (SILC project ) is part of this action plan. The SILC project will assess strategies to increase the maintenance of breastfeeding. The research will consist of a three arm cluster randomised control trial. It will determine if home visiting by a Maternal and Child Health Nurse (MCHN) for women with breastfeeding issues increases the maintenance of breastfeeding, and then if a drop-in centre additional to the home-visiting further enhances breastfeeding rates. The three arms of the trial will consist of a comparison (control) group receiving standard care, a targeted home-visiting group receiving home-based breastfeeding support visits by a MCHN and the third group receiving the targeted home visits plus access to a facilitated local drop-in centre.
Interventions
There are two intervention groups. One group receives early home-based breastfeeding support by a Maternal and Child Health Nurse (MCHN). The second intervention group receives early home-based breastfeeding support by a MCHN and access to a community-based breastfeeding drop-in centre. Participating MCHNs will have clinical experience in diagnosing and managing common breastfeeding problems: insufficient milk, perceived insufficient milk, nipple pain and damage, breast engorgement and mastitis, nipple/breast thrush, infant tongue-tie. They will assist the mother by giving advice and support, and suggesting appropriate referrals where necessary. It will be up to the allocated MCHN to determine the number and timing of support visits for each woman referred, however, it is anticipated that on average this will be two visits. It is anticipated that up to a third of women in intervention LGAs are likely to receive the home visiting intervention. The second intervention group will also have access to a community-based breastfeeding drop-in centre. These drop-in centres will operate for the duration of the trial intervention and women can visit them as many times as they wish. The number of days and hours the drop-in centres operate will be affected by number of births in the LGA and availability of a venue.
Sponsors
Study design
Eligibility
Inclusion criteria
- LGAs with a low breastfeeding rate for ‘any’ breastfeeding at discharge from hospital - LGAs who agree to participate and be randomised
Exclusion criteria
- LGAs with substantial initiatives (at the time of LGA selection) to increase breastfeeding duration or other substantial early childhood interventions - LGAs where participation is not feasible given the low number of births