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青少年使用可穿戴睡眠脑电图设备的可行性和可接受性:观察性研究

Feasibility and Acceptability of Wearable Sleep Electroencephalogram Device Use in Adolescents: Observational Study.

作者信息

Lunsford-Avery Jessica R, Keller Casey, Kollins Scott H, Krystal Andrew D, Jackson Leah, Engelhard Matthew M

机构信息

Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, United States.

Departments of Psychiatry and Neurology, University of California San Francisco School of Medicine, San Francisco, CA, United States.

出版信息

JMIR Mhealth Uhealth. 2020 Oct 1;8(10):e20590. doi: 10.2196/20590.

Abstract

BACKGROUND

Adolescence is an important life stage for the development of healthy behaviors, which have a long-lasting impact on health across the lifespan. Sleep undergoes significant changes during adolescence and is linked to physical and psychiatric health; however, sleep is rarely assessed in routine health care settings. Wearable sleep electroencephalogram (EEG) devices may represent user-friendly methods for assessing sleep among adolescents, but no studies to date have examined the feasibility and acceptability of sleep EEG wearables in this age group.

OBJECTIVE

The goal of the research was to investigate the feasibility and acceptability of sleep EEG wearable devices among adolescents aged 11 to 17 years.

METHODS

A total of 104 adolescents aged 11 to 17 years participated in 7 days of at-home sleep recording using a self-administered wearable sleep EEG device (Zmachine Insight+, General Sleep Corporation) as well as a wristworn actigraph. Feasibility was assessed as the number of full nights of successful recording completed by adolescents, and acceptability was measured by the wearable acceptability survey for sleep. Feasibility and acceptability were assessed separately for the sleep EEG device and wristworn actigraph.

RESULTS

A total of 94.2% (98/104) of adolescents successfully recorded at least 1 night of data using the sleep EEG device (mean number of nights 5.42; SD 1.71; median 6, mode 7). A total of 81.6% (84/103) rated the comfort of the device as falling in the comfortable to mildly uncomfortable range while awake. A total of 40.8% (42/103) reported typical sleep while using the device, while 39.8% (41/103) indicated minimal to mild device-related sleep disturbances. A minority (32/104, 30.8%) indicated changes in their sleep position due to device use, and very few (11/103, 10.7%) expressed dissatisfaction with their experience with the device. A similar pattern was observed for the wristworn actigraph device.

CONCLUSIONS

Wearable sleep EEG appears to represent a feasible, acceptable method for sleep assessment among adolescents and may have utility for assessing and treating sleep disturbances at a population level. Future studies with adolescents should evaluate strategies for further improving usability of such devices, assess relationships between sleep EEG-derived metrics and health outcomes, and investigate methods for incorporating data from these devices into emerging digital interventions and applications.

TRIAL REGISTRATION

ClinicalTrials.gov NCT03843762; https://clinicaltrials.gov/ct2/show/NCT03843762.

摘要

背景

青春期是健康行为发展的重要生命阶段,这些行为会对一生的健康产生持久影响。睡眠在青春期会发生显著变化,且与身体和精神健康相关;然而,在常规医疗保健环境中很少对睡眠进行评估。可穿戴睡眠脑电图(EEG)设备可能是评估青少年睡眠的用户友好型方法,但迄今为止尚无研究考察睡眠EEG可穿戴设备在该年龄组中的可行性和可接受性。

目的

本研究的目的是调查11至17岁青少年对睡眠EEG可穿戴设备的可行性和可接受性。

方法

共有104名11至17岁的青少年使用自我管理的可穿戴睡眠EEG设备(Zmachine Insight +,通用睡眠公司)以及腕部活动记录仪进行了7天的居家睡眠记录。可行性通过青少年完成的成功记录的完整夜晚数量来评估,可接受性通过睡眠可穿戴设备可接受性调查来衡量。分别对睡眠EEG设备和腕部活动记录仪的可行性和可接受性进行评估。

结果

共有94.2%(98/104)的青少年使用睡眠EEG设备成功记录了至少1晚的数据(平均夜晚数为5.42;标准差为1.71;中位数为6,众数为7)。共有81.6%(84/103)的青少年将设备在清醒时的舒适度评为舒适至轻度不舒适范围。共有40.8%(42/103)的青少年报告在使用设备时睡眠正常,而39.8%(41/103)的青少年表示与设备相关的睡眠干扰最小至轻度。少数(32/104,30.8%)青少年表示因使用设备而改变了睡眠姿势,很少有(11/103,10.7%)青少年对使用该设备的体验表示不满。腕部活动记录仪设备也观察到类似的模式。

结论

可穿戴睡眠EEG似乎是一种可行、可接受的青少年睡眠评估方法,可能对在人群层面评估和治疗睡眠障碍有用。未来针对青少年的研究应评估进一步提高此类设备可用性的策略,评估睡眠EEG衍生指标与健康结果之间的关系,并研究将这些设备的数据纳入新兴数字干预措施和应用的方法。

试验注册

ClinicalTrials.gov NCT03843762;https://clinicaltrials.gov/ct2/show/NCT03843762

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e19b/7563632/543e0068a3f6/mhealth_v8i10e20590_fig1.jpg

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