在预防肥胖的背景下,优化儿童睡眠促进的干预成分:SLEEPY 2.0研究方案

Maddy Fair, Jessica Decker, Alexander G. Fiks, Stephanie Mayne, Knashawn H. Morales, Ariel A. Williamson, Jonathan A. Mitchell
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引用次数: 0

摘要

背景:睡眠时间不足在儿童时期非常普遍,并与肥胖有关,尤其是在中学儿童中。初级保健环境在促进睡眠方面具有巨大的潜力,但面对面预约时有限的时间和睡眠资源是主要障碍。数字卫生创新为这些障碍提供了解决方案。可以开发移动卫生平台,在家庭环境中远程提供行为睡眠促进,并根据个人和环境因素进行调整,以帮助确保在社会人口群体中公平有效。本文提出了一项使用多阶段优化策略(MOST)的随机优化试验方案,以开发儿科护理设置的移动健康平台,以促进儿童肥胖预防的更长的睡眠时间。方法:这是一项在费城儿童医院进行的单点研究。我们将随机选取325名8-12岁的儿童,他们的身体质量指数(BMI)在50 - 95百分位数之间,每晚睡眠时间为8.5小时。“健康之路”移动平台将促进远程通信和数据收集。睡眠追踪器将评估12个月的睡眠模式(2周的磨合期;6个月的干预;≈5.5月后续)。随机24因子设计将评估四个组成部分:睡眠目标(比基线睡眠时间≥9小时或≥30分钟)、数字指导(主动或主动与虚拟研究访问)、照顾者激励(主动或不主动)和表现反馈(主动或不主动)。在基线、6个月和12个月时使用双能x线吸收仪测量脂肪量。在基线、6个月和12个月的24小时饮食回顾中,测量总能量摄入、膳食时间和组成。社会人口统计数据(如性别、种族、民族)将通过自我报告来衡量,家庭住址将进行地理编码,用于地理空间分析。我们预计这项创新的优化试验将确定促进儿童睡眠的最佳成分设置,并在临床上有意义的改善脂肪质量轨迹。重要的是,该平台将通过促进社会人口群体的睡眠健康公平产生广泛的影响。确定了最佳设置后,我们将能够在未来的随机对照试验中确定MOST框架评估阶段下最终干预方案的有效性。我们提出的研究将极大地推动行为睡眠医学领域的发展,并重新设想如何在儿科医疗保健中预防睡眠不足和肥胖。临床试验注册:ClinicalTrials.gov NCT05703347注册于2023年1月30日。
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Optimizing intervention components for sleep promotion in children in the context of obesity prevention: the SLEEPY 2.0 study protocol
Background Insufficient sleep duration is highly prevalent in childhood and is associated with obesity, especially among middle school-aged children. The primary care setting has enormous potential to promote sleep, but limited time and sleep resources at in person appointments are key barriers. Digital health innovations offer solutions to these barriers. Mobile health platforms can be developed to deliver behavioral sleep promotion remotely in the home setting, with tailoring to individual and contextual factors to help ensure equitable effectiveness across sociodemographic groups. This paper presents the protocol for a randomized optimization trial using the Multiphase Optimization Strategy (MOST) to develop a mobile health platform for the pediatric care setting to promote longer sleep duration for childhood obesity prevention. Methods This is a single-site study being conducted at the Children's Hospital of Philadelphia. We will randomize 325 children, aged 8–12 y, with a body mass index (BMI) between the 50th−95th percentile, and who sleep <8.5 h per night. The Way to Health mobile platform will facilitate remote communication and data collection. A sleep tracker will estimate sleep patterns for 12-months (2-week run-in; 6-month intervention; ≈5.5-month follow-up). A randomized 2 4 factorial design will assess four components: sleep goal (≥9 h or ≥30 min above baseline sleep duration), digital guidance (active or active with virtual study visits), caregiver incentive (inactive or active), and performance feedback (inactive or active). Fat mass will be measured at baseline, 6-, and 12-months using dual energy X-ray absorptiometry. Total energy intake and the timing and composition of meals will be measured using 24-h dietary recalls at baseline, 6-, and 12-months. Sociodemographic data (e.g., sex, race, ethnicity) will be measured using self-report and home addresses will be geocoded for geospatial analyses. Discussion We anticipate that this innovative optimization trial will identify optimal component settings for sleep promotion in children, with clinically meaningful improvements in fat mass trajectories. Importantly, the platform will have broad impact by promoting sleep health equity across sociodemographic groups. With the optimal settings identified, we will be able to determine the effectiveness of the final intervention package under the evaluation phase of the MOST framework in a future randomized controlled trial. Our proposed research will greatly advance the field of behavioral sleep medicine and reimagine how insufficient sleep duration and obesity are prevented in pediatric healthcare. Trial registration ClinicalTrials.gov NCT05703347 registered on 30 January 2023.
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