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痴呆相关睡眠干预手册(DREAMS START)与常规护理对痴呆患者及其照护者的临床效果比较:一项单盲、3 期、平行臂、优效性随机对照试验。

Clinical effectiveness of DREAMS START (Dementia Related Manual for Sleep; Strategies for Relatives) versus usual care for people with dementia and their carers: a single-masked, phase 3, parallel-arm, superiority randomised controlled trial.

机构信息

Division of Psychiatry, University College London, London, UK; Camden and Islington NHS Foundation Trust, London, UK.

Division of Psychiatry, University College London, London, UK.

出版信息

Lancet Healthy Longev. 2024 Oct;5(10):100635. doi: 10.1016/j.lanhl.2024.08.004. Epub 2024 Oct 1.

Abstract

BACKGROUND

Sleep disturbances are common and distressing for people with dementia and their families. Non-pharmacological interventions should be first-line management, avoiding harmful pharmacological side-effects, but there is none with known effectiveness. We aimed to establish whether DREAMS START, a multicomponent intervention, reduced sleep disturbance in people with dementia living at home compared with usual care.

METHODS

We conducted a phase 3, two-arm, multicentre, parallel-arm, superiority randomised controlled trial with masked outcome assessment, recruiting dyads of people with dementia and sleep disturbance and family carers from community settings. Randomisation to the DREAMS START intervention (plus usual treatment) or usual treatment was conducted at dyadic level, blocked, and stratified by site, with a web-based system assigning allocation. DREAMS START is a six-session, manualised intervention delivered face to face or remotely by non-clinically trained graduates over an approximately 3-month period. The primary outcome was sleep disturbance measured by the Sleep Disorders Inventory (SDI) at 8 months. Analyses were on the intention-to-treat population. This trial is registered with ISRCTN 13072268.

FINDINGS

Between Feb 24, 2021, and March 5, 2023, 377 dyads were randomly assigned (1:1), 189 to usual treatment and 188 to intervention. The mean age of participants with dementia was 79·4 years (SD 9·0), and 206 (55%) were women. The mean SDI score at 8 months was lower in the intervention group compared with the usual treatment group (15·16 [SD 12·77], n=159, vs 20·34 [16·67], n=163]; adjusted difference in means -4·70 [95% CI -7·65 to -1·74], p=0·002). 17 (9%) people with dementia in the intervention group and 17 (9%) in the control group died during the trial; the deaths were unrelated to the intervention.

INTERPRETATION

To our knowledge, DREAMS START is the first multicomponent intervention to improve the sleep of people living at home with dementia more than usual clinical care. It had sustained effectiveness beyond intervention delivery. The intervention's delivery by non-clinically trained graduates increases the potential for implementation within health services, adding to usual clinical care.

FUNDING

National Institute for Health and Care Research Health Technology Assessment.

摘要

背景

睡眠障碍在痴呆症患者及其家属中很常见且令人痛苦。非药物干预措施应作为一线治疗方法,避免药物的有害副作用,但目前尚无已知有效的治疗方法。我们旨在确定多组分干预措施 DREAMS START 是否能减少居家痴呆症患者的睡眠障碍,与常规护理相比。

方法

我们进行了一项为期 3 期、双盲、多中心、平行臂、优势随机对照试验,对来自社区环境的痴呆症患者及其睡眠障碍和家庭照顾者进行了双人评估。DREAMS START 干预(加常规治疗)或常规治疗的随机分组在双人水平上进行,采用基于网络的系统进行分组,采用分组、分层的方式进行,以站点为单位进行分组。DREAMS START 是一项六节、手册化的干预措施,由非临床培训的毕业生在大约 3 个月的时间内进行面对面或远程授课。主要结局是通过睡眠障碍量表(SDI)在 8 个月时测量的睡眠障碍。分析是基于意向治疗人群。这项试验在 ISRCTN 注册,编号为 ISRCTN66602251。

结果

在 2021 年 2 月 24 日至 2023 年 3 月 5 日期间,共随机分配了 377 对(1:1),189 对接受常规治疗,188 对接受干预。痴呆症患者的平均年龄为 79.4 岁(标准差为 9.0),206 人(55%)为女性。8 个月时,干预组的 SDI 评分低于常规治疗组(15.16 [标准差 12.77],n=159,vs 20.34 [16.67],n=163];调整后的平均差异-4.70 [95%CI-7.65 至-1.74],p=0.002)。在试验过程中,干预组有 17 名(9%)痴呆症患者和对照组有 17 名(9%)患者死亡;这些死亡与干预无关。

解释

据我们所知,DREAMS START 是第一个改善居家痴呆症患者睡眠的多组分干预措施,比常规临床护理效果更好。它在干预措施实施后仍具有持续的效果。非临床培训毕业生提供干预措施增加了在卫生服务中实施的可能性,增加了常规临床护理。

资金来源

英国国家卫生与保健优化研究所健康技术评估。

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