Effectiveness and cost-effectiveness of Assets-based feeding help Before and After birth (ABA-feed) for improving breastfeeding initiation and continuation: protocol for a multicentre randomised controlled trial (Version 3.0)

Author:

Clarke JoanneORCID,Dombrowski Stephan UORCID,Gkini Eleni,Hoddinott PatORCID,Ingram JennyORCID,MacArthur Christine,Moss Ngawai,Ocansey Laura,Roberts Tracy,Thomson GillianORCID,Sanders Julia,Sitch Alice J,Stubbs Clive,Taylor Beck,Tearne Sarah,Woolley Rebecca,Jolly KateORCID

Abstract

IntroductionBreastfeeding has health benefits for infants and mothers, yet the UK has low rates with marked social inequalities. The Assets-based feeding help Before and After birth (ABA) feasibility study demonstrated the acceptability of a proactive, assets-based, woman-centred peer support intervention, inclusive of all feeding types, to mothers, peer supporters and maternity services. The ABA-feed study aims to assess the clinical and cost-effectiveness of the ABA-feed intervention compared with usual care in first-time mothers in a full trial.Methods and analysisA multicentre randomised controlled trial with economic evaluation to explore clinical and cost-effectiveness, and embedded process evaluation to explore differences in implementation between sites. We aim to recruit 2730 primiparous women, regardless of feeding intention. Women will be recruited at 17 sites from antenatal clinics and various remote methods including social media and invitations from midwives and health visitors. Women will be randomised at a ratio of 1.43:1 to receive either ABA-feed intervention or usual care. A train the trainer model will be used to train local Infant Feeding Coordinators to train existing peer supporters to become ‘infant feeding helpers’ in the ABA-feed intervention. Infant feeding outcomes will be collected at 3 days, and 8, 16 and 24 weeks postbirth. The primary outcome will be any breastfeeding at 8 weeks postbirth. Secondary outcomes will include breastfeeding initiation, any and exclusive breastfeeding, formula feeding practices, anxiety, social support and healthcare utilisation. All analyses will be based on the intention-to-treat principle.Ethics and disseminationThe study protocol has been approved by the East of Scotland Research Ethics Committee. Trial results will be available through open-access publication in a peer-reviewed journal and presented at relevant meetings and conferences.Trial registration numberISRCTN17395671.

Funder

Public Health Research Programme

NIHR Applied Research Collaboration West Midlands

NIHR Birmingham Biomedical Research Centre at the University Hospitals Birmingham NHS Foundation Trust

Publisher

BMJ

Subject

General Medicine

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