Division of Public Health and Department of Obstetrics, Gynecology, and Reproductive Biology, Michigan State University, Flint, Michigan, USA
Family Medicine and Public Health Sciences, Wayne State University School of Medicine, Detroit, Michigan, USA.
BMJ Open. 2022 Aug 3;12(8):e062735. doi: 10.1136/bmjopen-2022-062735.
Approximately 1 in 7 pregnant women in the USA report past-month alcohol use. Strong evidence connects prenatal alcohol exposure with a range of adverse perinatal outcomes, including the spectrum of conditions known as fetal alcohol spectrum disorders. Screening and Brief Intervention (SBI) has been recommended for pregnant women but has proven difficult to implement. This study will test the efficacy of single-session technology-delivered SBI (electronic SBI) for alcohol use in pregnancy, while simultaneously evaluating the possible additional benefit of tailored text messages and/or booster sessions in a 3×2 factorial trial.
This full factorial trial will use online advertising and clinic-based flyers to recruit pregnant women meeting criteria for unhealthy alcohol use, and randomly assign them to one of six conditions crossing three levels of brief intervention (none, single 120-minute session and single session plus two 5-minute boosters) with two levels of tailored text messaging (none vs twice weekly messages). The primary analysis will test for dose-response effects of the brief intervention on alcohol abstinence, defined as no self-report of alcohol use in the 90 days prior to 34 weeks' gestation, and negative results for ethyl glucuronide analysis of fingernail samples. Secondary analyses will examine main and interaction effects of tailored text messaging as well as intervention effects on birth outcomes.
Ethical approval was provided by the Michigan State University Biomedical and Health Institutional Review Board (STUDY00005298). Results will be presented at conferences and community forums, in addition to being published in a peer-reviewed journal. Intervention content demonstrating sufficient efficacy and safety will be made publicly available.
ClinicalTrials.gov Registry (NCT04332172).
在美国,大约每 7 名孕妇中就有 1 名报告过去一个月有饮酒行为。大量证据表明,产前酒精暴露与一系列围产期不良结局有关,包括一系列被称为胎儿酒精谱系障碍的疾病。筛查和简短干预(SBI)已被推荐用于孕妇,但事实证明难以实施。本研究将测试单次使用技术提供的 SBI(电子 SBI)对妊娠期间饮酒的疗效,同时在 3×2 析因试验中评估定制短信和/或强化疗程的可能额外益处。
这项完全析因试验将使用在线广告和诊所传单招募符合不健康饮酒标准的孕妇,并将她们随机分配到以下六组之一:无干预、单次 120 分钟疗程和单次疗程加两次 5 分钟强化疗程,以及两种定制短信水平(无 vs 每周两次消息)。主要分析将测试简短干预对酒精禁欲的剂量反应效果,定义为在 34 周妊娠前 90 天内无自我报告饮酒,以及指甲样本乙基葡萄糖醛酸分析的阴性结果。次要分析将检查定制短信的主要和交互作用以及干预对出生结局的影响。
密歇根州立大学生物医学和健康机构审查委员会(STUDY00005298)已批准该研究的伦理。结果将在会议和社区论坛上展示,并发表在同行评议的期刊上。表现出足够疗效和安全性的干预内容将公开提供。
ClinicalTrials.gov 注册表(NCT04332172)。