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“狮子”研究的可行性与可接受性:一项在退伍军人事务部(VA)开展的完全远程的随机临床试验,旨在对有或无创伤性脑损伤(TBI)的退伍军人进行光疗以改善睡眠,由军事创伤性脑损伤(MTBI)赞助的方案。

Feasibility and acceptability for LION, a fully remote, randomized clinical trial within the VA for light therapy to improve sleep in Veterans with and without TBI: An MTBI sponsored protocol.

作者信息

Elliott Jonathan E, Brewer Jessica S, Keil Allison T, Ligman Brittany R, Bryant-Ekstrand Mohini D, McBride Alisha A, Powers Katherine, Sicard Savanah J, Twamley Elizabeth W, O'Neil Maya E, Hildebrand Andrea D, Nguyen Thuan, Morasco Benjamin J, Gill Jessica M, Dengler Bradley A, Lim Miranda M

机构信息

VA Portland Health Care System, Portland, OR, USA.

Oregon Health & Science University, Department of Neurology, Portland, OR, USA.

出版信息

medRxiv. 2024 May 31:2024.05.30.24308195. doi: 10.1101/2024.05.30.24308195.

Abstract

Sleep-wake disturbances frequently present in Veterans with mild traumatic brain injury (mTBI). These TBI-related sleep impairments confer significant burden and commonly exacerbate other functional impairments. Therapies to improve sleep following mTBI are limited and studies in Veterans are even more scarce. In our previous pilot work, morning bright light therapy (MBLT) was found to be a feasible behavioral sleep intervention in Veterans with a history of mTBI; however, this was single-arm, open-label, and non-randomized, and therefore was not intended to establish efficacy. The present study, LION (light vs ion therapy) extends this preliminary work as a fully powered, sham-controlled, participant-masked randomized controlled trial (NCT03968874), implemented as fully remote within the VA (target n=120 complete). Randomization at 2:1 allocation ratio to: 1) active: MBLT (n=80), and 2) sham: deactivated negative ion generator (n=40); each with identical engagement parameters (60-min duration; within 2-hrs of waking; daily over 28-day duration). Participant masking via deception balanced expectancy assumptions across arms. Outcome measures were assessed following a 14-day baseline (pre-intervention), following 28-days of device engagement (post-intervention), and 28-days after the post-intervention assessment (follow-up). Primary outcomes were sleep measures, including continuous wrist-based actigraphy, self-report, and daily sleep dairy entries. Secondary/exploratory outcomes included cognition, mood, quality of life, circadian rhythm via dim light melatonin onset, and biofluid-based biomarkers. Participant drop out occurred in <10% of those enrolled, incomplete/missing data was present in <15% of key outcome variables, and overall fidelity adherence to the intervention was >85%, collectively establishing feasibility and acceptability for MBLT in Veterans with mTBI.

摘要

睡眠-觉醒障碍在轻度创伤性脑损伤(mTBI)退伍军人中经常出现。这些与创伤性脑损伤相关的睡眠障碍带来了巨大负担,并且通常会加重其他功能障碍。改善mTBI后睡眠的疗法有限,针对退伍军人的研究更为稀少。在我们之前的试点工作中,发现早晨强光疗法(MBLT)对有mTBI病史的退伍军人来说是一种可行的行为睡眠干预措施;然而,这是一项单臂、开放标签且非随机的研究,因此并非旨在确定其疗效。目前的LION(光与离子疗法)研究将这项初步工作扩展为一项完全有统计学效力、设假对照、参与者盲法的随机对照试验(NCT03968874),在退伍军人事务部(VA)内部完全远程实施(目标n = 120例完成)。按2:1的分配比例随机分为:1)活性组:MBLT(n = 80),以及2)假对照组:停用负离子发生器(n = 40);每组具有相同的参与参数(持续60分钟;醒来后2小时内;每天进行28天)。通过欺骗手段使参与者保持盲法,平衡了各组之间的预期假设。在14天基线期(干预前)、设备使用28天(干预后)以及干预后评估28天后(随访)对结果指标进行评估。主要结果指标是睡眠指标,包括基于手腕的连续活动记录仪监测结果、自我报告以及每日睡眠日记记录。次要/探索性结果指标包括认知、情绪、生活质量、通过暗光褪黑素开始分泌时间评估的昼夜节律以及基于生物流体的生物标志物。参与研究的人员中退出率低于10%,关键结果变量中存在不完整/缺失数据的比例低于15%,并且总体上对干预措施的依从性超过85%,共同证明了MBLT在mTBI退伍军人中的可行性和可接受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a23/11160858/d916c4f6e108/nihpp-2024.05.30.24308195v1-f0001.jpg

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