An assets-based intervention before and after birth to improve breastfeeding initiation and continuation: the ABA feasibility RCT

Author:

Clarke Joanne L1ORCID,Ingram Jenny2ORCID,Johnson Debbie2ORCID,Thomson Gill3ORCID,Trickey Heather4ORCID,Dombrowski Stephan U56ORCID,Sitch Alice1ORCID,Dykes Fiona3ORCID,Feltham Max G7ORCID,MacArthur Christine1ORCID,Roberts Tracy8ORCID,Hoddinott Pat9ORCID,Jolly Kate1ORCID

Affiliation:

1. Institute of Applied Health Research, University of Birmingham, Birmingham, UK

2. Centre for Academic Child Health, University of Bristol, Bristol, UK

3. Maternal and Infant Nutrition and Nurture Unit (MAINN), University of Central Lancashire, Preston, UK

4. Development and Evaluation of Complex Public Health Interventions (DECIPHeR), Department of Social Medicine, Cardiff University, Cardiff, UK

5. Faculty of Kinesiology, University of New Brunswick, Fredericton, NB, Canada

6. Department of Psychology, University of Stirling, Stirling, UK

7. Birmingham Clinical Trials Unit, University of Birmingham, Birmingham, UK

8. Health Economic Unit, University of Birmingham, Birmingham, UK

9. Nursing, Midwifery and Allied Health Professions Research Unit, University of Stirling, Stirling, UK

Abstract

Background The UK has low levels of breastfeeding initiation and continuation, with evident socioeconomic disparities. To be inclusive, peer-support interventions should be woman-centred rather than breastfeeding-centred. Assets-based approaches to public health focus on the positive capabilities of individuals and communities, rather than their deficits and problems. The Assets-based feeding help Before and After birth (ABA) intervention offers an assets-based approach based on behaviour change theory. Objective To investigate the feasibility of delivering the ABA infant feeding intervention in a randomised controlled trial. Design This was an individually randomised controlled feasibility trial; women were randomised in a 1 : 1 ratio to either the intervention group or the comparator (usual care) group. Setting Two separate English sites were selected because they had an existing breastfeeding peer support service, relatively high levels of socioeconomic disadvantage and low rates of breastfeeding. Participants Women aged ≥ 16 years who were pregnant with their first child, irrespective of feeding intention (n = 103), were recruited by researchers in antenatal clinics. Interventions Proactive, woman-centred support, using an assets-based approach and including behaviour change techniques, was provided by an infant-feeding helper (a breastfeeding peer supporter trained in the ABA intervention) and delivered through face-to-face contact, telephone conversations and text messages. The intervention commenced at around 30 weeks’ gestation and could continue until 5 months postnatally. Main outcome measures The main outcome measures were feasibility of intervention delivery with the requisite intensity and duration; acceptability to women, infant-feeding helpers and maternity services; and feasibility of a future randomised controlled trial. Outcomes included recruitment rates and follow-up rates at 3 days, 8 weeks and 6 months postnatally, and outcomes for a future full trial were collected via participant questionnaires. A mixed-methods process evaluation included qualitative interviews with women, infant-feeding helpers and maternity services; infant-feeding helper logs; and audio-recordings of antenatal contacts to check intervention fidelity. Results Of the 135 eligible women approached, 103 (76.3%) agreed to participate. The study was successful in recruiting teenagers (8.7%) and women living in areas of socioeconomic disadvantage (37.3% resided in the most deprived 40% of small areas in England). Postnatal follow-up rates were 68.0%, 85.4% and 80.6% at 3 days, 8 weeks and 6 months, respectively. Feeding status at 8 weeks was obtained for 95.1% of participants. Recruitment took place from February 2017 until August 2017. It was possible to recruit and train existing peer supporters to the infant-feeding helper role. The intervention was delivered to most women with relatively high fidelity. Among the 50 women in the intervention group, 39 received antenatal visits and 40 received postnatal support. Qualitative data showed that the intervention was acceptable. There was no evidence of intervention-related harms. Limitations Birth notification delays resulted in delays in the collection of postnatal feeding status data and in the offer of postnatal support. In addition, the intervention needs to better consider all infant-feeding types and did not adequately accommodate women who delivered prematurely. Conclusion It is feasible to deliver the intervention and trial. Future work The intervention should be tested in a fully powered randomised controlled trial. Trial registration Current Controlled Trials ISRCTN14760978. Funding This project was funded by the National Institute for Health Research (NIHR) Public Health Research programme and will be published in full in Public Health Research; Vol. 8, No. 7. See the NIHR Journals Library website for further project information.

Funder

Public Health Research programme

Publisher

National Institute for Health Research

Subject

Pharmacology (medical),Complementary and alternative medicine,Pharmaceutical Science

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