出生前后基于资产的干预以改善母乳喂养的开始和持续:ABA可行性随机对照试验

J. Clarke, J. Ingram, Debbie Johnson, G. Thomson, H. Trickey, S. Dombrowski, A. Sitch, F. Dykes, M. Feltham, C. MacArthur, T. Roberts, P. Hoddinott, K. Jolly
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引用次数: 4

摘要

英国母乳喂养的开始和持续程度较低,社会经济差异明显。为了具有包容性,同伴支持干预措施应该以妇女为中心,而不是以母乳喂养为中心。基于资产的公共卫生方法侧重于个人和社区的积极能力,而不是他们的缺陷和问题。基于资产的喂养帮助出生前后(ABA)干预提供了一种基于行为改变理论的基于资产的方法。在一项随机对照试验中研究ABA婴儿喂养干预的可行性。这是一项单独随机对照的可行性试验;女性被随机分为1组 : 干预组或对照组(常规护理)的比例为1。之所以选择两个独立的英语网站,是因为它们有现有的母乳喂养同伴支持服务,社会经济劣势相对较高,母乳喂养率较低。年龄≥ 怀孕16岁的第一个孩子,无论喂养意图如何(n = 103),由产前诊所的研究人员招募。由一名婴儿喂养助手(接受过美国律师协会干预培训的母乳喂养同伴支持者)提供以妇女为中心的积极支持,采用基于资产的方法,包括行为改变技术,并通过面对面接触、电话交谈和短信提供。干预从妊娠30周左右开始,可以持续到产后5个月。主要的成果衡量标准是以必要的强度和持续时间进行干预的可行性;妇女、婴儿喂养助手和产妇服务的可接受性;以及未来随机对照试验的可行性。结果包括出生后3天、8周和6个月的招募率和随访率,并通过参与者问卷收集未来完整试验的结果。混合方法过程评估包括对妇女、婴儿喂养助理和产妇服务进行定性访谈;婴儿喂养辅助日志;以及产前接触的录音,以检查干预的保真度。在135名符合条件的妇女中,103人(76.3%)同意参加。这项研究成功地招募了生活在社会经济劣势地区的青少年(8.7%)和妇女(37.3%居住在英格兰40%最贫困的小地区)。产后3天、8周和6个月的随访率分别为68.0%、85.4%和80.6%。95.1%的参与者在8周时获得了进食状态。招聘时间为2017年2月至2017年8月。可以招募和培训现有的同伴支持者担任婴儿喂养助手的角色。该干预措施以相对较高的忠诚度提供给了大多数女性。在干预组的50名妇女中,39人接受了产前检查,40人接受了产后支持。定性数据表明,干预是可以接受的。没有证据表明干预会造成伤害。出生通知延迟导致产后喂养状况数据的收集和产后支持的提供延迟。此外,干预措施需要更好地考虑所有婴儿喂养类型,并且没有充分照顾早产的妇女。提供干预和试验是可行的。干预措施应在一项完全有效的随机对照试验中进行测试。当前对照试验ISRCTN14760978。该项目由国家卫生研究所公共卫生研究计划资助,并将在《公共卫生研究》上全文发表;第8卷第7期。有关更多项目信息,请访问NIHR期刊图书馆网站。
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An assets-based intervention before and after birth to improve breastfeeding initiation and continuation: the ABA feasibility RCT
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. To investigate the feasibility of delivering the ABA infant feeding intervention in a randomised controlled trial. 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. 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. Women aged ≥ 16 years who were pregnant with their first child, irrespective of feeding intention (n = 103), were recruited by researchers in antenatal clinics. 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. 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. 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. 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. It is feasible to deliver the intervention and trial. The intervention should be tested in a fully powered randomised controlled trial. Current Controlled Trials ISRCTN14760978. 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.
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