Acceptability of digital health intervention during pregnancy to inform women about postpartum contraception (DIGICAP): a pilot randomised controlled study.

IF 3.4 3区 医学 Q1 FAMILY STUDIES
Michelle Cooper, Caroline J Free, Kevin Ka-Wing Kuan, Karen McCabe, Emmanuela Osei-Asemani, Charles Opondo, Sharon Cameron
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引用次数: 0

Abstract

Background: Pregnancy within a year of childbirth has negative impacts on women and their children's health. We developed a digital health intervention (DHI) to empower women in contraceptive choices postpartum. Our pilot randomised controlled trial (RCT) aimed to establish the feasibility of a main RCT of the effects of the DHI compared with standard care on long-acting contraception use.

Methods: Our pilot RCT recruited 52, 20-24 weeks pregnant women in NHS Lothian, UK between October 2022 and April 2023. Participants were randomised 7:3 to receive either the DHI (n=37) in addition to standard care, or standard care alone (n=15). Telephone survey follow-up was at 24 weeks' gestation and 6 weeks postpartum. Semi-structured qualitative interviews (n=10) were conducted with participants receiving the DHI.

Results: All eligible women joined the study and completed follow-up. All intervention participants found the animation highly acceptable; one participant requested text message discontinuation. We completed followed up on 37/37 (100%) of participants. DHI participants reported they valued access to credible contraceptive information that supported decision making in a non-pressurised way.

Conclusions: Our DHI is highly acceptable and a trial is feasible. A larger trial is needed to establish if the DHI increases uptake of long-acting reversible contraception postpartum and reduces unintended pregnancies within 12 months of childbirth.

Trial registration number: (Trial registration ISRCTN48521918).

怀孕期间数字健康干预的可接受性,以告知妇女产后避孕(DIGICAP):一项试点随机对照研究
背景:分娩后一年内怀孕对妇女及其子女的健康有负面影响。我们开发了一种数字健康干预(DHI),赋予妇女产后避孕选择的权力。我们的试点随机对照试验(RCT)旨在建立DHI与标准护理对长效避孕药使用影响的主要RCT的可行性。方法:我们的试点RCT在2022年10月至2023年4月期间在英国洛锡安NHS招募了52名20-24周的孕妇。参与者按7:3随机分组,接受DHI (n=37)和标准治疗,或单独接受标准治疗(n=15)。电话调查随访于妊娠24周和产后6周。对接受DHI的参与者进行半结构化定性访谈(n=10)。结果:所有符合条件的女性都加入了研究并完成了随访。所有的干预参与者都认为动画是高度可接受的;一位与会者要求停止发短信。我们对37/37(100%)的参与者完成了随访。DHI参与者报告说,他们重视获得可靠的避孕信息,以非压力的方式支持决策。结论:我们的DHI是高度可接受的,试验是可行的。需要更大规模的试验来确定DHI是否增加了产后长效可逆避孕的使用,并减少了分娩12个月内的意外怀孕。试验注册号:(试验注册号ISRCTN48521918)。
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来源期刊
BMJ Sexual & Reproductive Health
BMJ Sexual & Reproductive Health Medicine-Reproductive Medicine
CiteScore
5.10
自引率
6.10%
发文量
38
期刊介绍: BMJ Sexual & Reproductive Health is a multiprofessional journal that promotes sexual and reproductive health and wellbeing, and best contraceptive practice, worldwide. It publishes research, debate and comment to inform policy and practice, and recognises the importance of professional-patient partnership.
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