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一项务实有效性随机对照试验,针对入住病房的急性精神疾病跨诊断样本患者,该病房的晚间照明要么是蓝光减少的,要么是正常照明条件,试验内容为精神科住院时长。

A pragmatic effectiveness randomized controlled trial of the duration of psychiatric hospitalization in a trans-diagnostic sample of patients with acute mental illness admitted to a ward with either blue-depleted evening lighting or normal lighting conditions.

作者信息

Scott Jan, Langsrud Knut, Vethe Daniel, Kjørstad Kaia, Vestergaard Cecilie L, Faaland Patrick, Lydersen Stian, Vaaler Arne, Morken Gunnar, Torgersen Terje, Kallestad Håvard

机构信息

Department of Mental Health, Norwegian University of Science and Technology, Trondheim, Norway.

Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.

出版信息

Trials. 2019 Aug 1;20(1):472. doi: 10.1186/s13063-019-3582-2.

Abstract

BACKGROUND

There is increasing recognition of the need to stabilize sleep-wake cycles in individuals with major mental disorders. As such, clinicians and researchers advocate the use of interventions targeted at sleep and circadian dysrhythmias as an adjunct to the standard treatments offered for acute illness episodes of a broad range of diagnoses. To determine the trans-diagnostic generalizability of chronotherapy, we explore the benefits of admitting individuals with an acute illness episode to a psychiatric inpatient unit where changes in light exposure are integrated into the therapeutic environment.

METHODS/DESIGN: A two-arm, pragmatic effectiveness, randomized controlled treatment trial, where individuals admitted for acute inpatient psychiatric care will be allocated to a ward with blue-depleted evening light or to a ward with the same layout and facilities but lacking the new lighting technology. The trial will test whether the experimental lighting conditions offer any additional benefits beyond those associated with usual treatment in an acute psychiatric inpatient unit. The main objectives are to examine any differences between groups in the mean duration of hospitalization in days. Additional analyses will compare group differences in symptoms, functioning, medication usage, and side effects and whether length of stay is associated with stability of sleep-wake cycles and circadian rhythms. Ancillary investigations should determine any benefits according to diagnostic subgroups and potential drawbacks such as any adverse effects on the well-being of professionals working across both wards.

DISCUSSION

This unit offers a unique opportunity to explore how exposure to different lighting conditions may modify sleep-wake cycles and how any changes in sleep-wake cycle may impact on the clinical and functional outcomes of individuals experiencing an acute episode of a severe mental disorder that requires inpatient care. The findings could influence the future design of hospital units offering care to patients with mental or physical disorders.

TRIAL REGISTRATION

ClinicalTrials.gov, ID: NCT03788993 . Retrospectively registered on 28 December 2018.

摘要

背景

人们越来越认识到稳定重度精神障碍患者的睡眠-觉醒周期的必要性。因此,临床医生和研究人员主张将针对睡眠和昼夜节律失调的干预措施作为广泛诊断的急性疾病发作的标准治疗的辅助手段。为了确定时间疗法的跨诊断普遍性,我们探讨了将急性疾病发作的患者收治到精神科住院单元的益处,在该单元中,光照暴露的变化被整合到治疗环境中。

方法/设计:一项双臂、务实有效性、随机对照治疗试验,因急性住院精神科护理入院的患者将被分配到一个夜间蓝光减少的病房或一个布局和设施相同但缺乏新照明技术的病房。该试验将测试实验性光照条件是否能提供超出急性精神科住院单元常规治疗相关益处的任何额外益处。主要目标是检查两组在住院天数的平均时长上是否存在差异。额外分析将比较两组在症状、功能、药物使用和副作用方面的差异,以及住院时长是否与睡眠-觉醒周期和昼夜节律的稳定性相关。辅助调查应根据诊断亚组确定任何益处以及潜在缺点,例如对两个病房工作的专业人员的幸福感的任何不利影响。

讨论

该单元提供了一个独特的机会来探索暴露于不同光照条件如何改变睡眠-觉醒周期,以及睡眠-觉醒周期的任何变化如何影响需要住院护理的严重精神障碍急性发作患者的临床和功能结局。研究结果可能会影响未来为患有精神或身体疾病的患者提供护理的医院单元的设计。

试验注册

ClinicalTrials.gov,标识符:NCT03788993。于2018年12月28日追溯注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6676579/bd37495b8341/13063_2019_3582_Fig1_HTML.jpg

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