Wearables

可穿戴设备
  • 文章类型: Journal Article
    目的:连续血糖监测仪(CGMs)在耐力运动员中越来越受欢迎,尽管准确性未经证实。我们评估了在休息时佩戴在2个不同部位的FreeStyleLibre2的并发有效性,在稳态运行期间,和餐后。
    方法:13种非糖尿病,训练有素的休闲跑步者(年龄=40[8]y,最大有氧耗氧量=46.1[6.4]mL·kg-1·min-1)在跑步机以50%的强度运行30、60和90分钟时,在上臂和胸部佩戴CGM,60%,和70%的最大有氧耗氧量,分别。通过手动扫描CGM并获得手指刺破的毛细血管血糖样品来测量葡萄糖。平均绝对相对差异,范围内的时间,和连续葡萄糖Clarke误差网格分析用于比较配对CGM和血糖读数。
    结果:在稳态运行的所有强度下,我们发现手臂的平均绝对相对差异为13.8(10.9),胸部的平均绝对相对差异为11.4(9.0).变异系数超过70%。大约47%的手臂和50%的胸部配对葡萄糖测量值的绝对差异≤10%。连续葡萄糖克拉克误差网格分析指示99.8%(手臂)和99.6%(胸部)CGM数据落在临床上可接受的区域A和B中。然而,CGM准确地检测平均葡萄糖读数随时间的趋势。
    结论:CGMs对于点血糖监测无效,但对于稳态运动期间的血糖趋势监测似乎有效。手臂和胸部的准确性相似。需要进一步的研究来确定CGM是否可以检测运动过程中的低血糖等重要事件。
    OBJECTIVE: Continuous glucose monitors (CGMs) are becoming increasingly popular among endurance athletes despite unconfirmed accuracy. We assessed the concurrent validity of the FreeStyle Libre 2 worn on 2 different sites at rest, during steady-state running, and postprandial.
    METHODS: Thirteen nondiabetic, well-trained recreational runners (age = 40 [8] y, maximal aerobic oxygen consumption = 46.1 [6.4] mL·kg-1·min-1) wore a CGM on the upper arm and chest while treadmill running for 30, 60, and 90 minutes at intensities corresponding to 50%, 60%, and 70% of maximal aerobic oxygen consumption, respectively. Glucose was measured by manually scanning CGMs and obtaining a finger-prick capillary blood glucose sample. Mean absolute relative difference, time in range, and continuous glucose Clarke error grid analysis were used to compare paired CGM and blood glucose readings.
    RESULTS: Across all intensities of steady-state running, we found a mean absolute relative difference of 13.8 (10.9) for the arm and 11.4 (9.0) for the chest. The coefficient of variation exceeded 70%. Approximately 47% of arm and 50% of chest paired glucose measurements had an absolute difference ≤10%. Continuous glucose Clarke error grid analysis indicated 99.8% (arm) and 99.6% (chest) CGM data fell in clinically acceptable zones A and B. Time-in-range analysis showed reduced accuracy at lower glucose levels. However, CGMs accurately detected trends in mean glucose readings over time.
    CONCLUSIONS: CGMs are not valid for point glucose monitoring but appear to be valid for monitoring glucose trends during steady-state exercise. Accuracy is similar for arm and chest. Further research is needed to determine whether CGMs can detect important events such as hypoglycemia during exercise.
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  • 文章类型: Journal Article
    在美国,大多数患有高血压的黑人女性拥有智能手机或平板电脑,并使用社交媒体,许多人使用可穿戴活动跟踪器和健康或保健应用程序,可用于支持生活方式改变和药物依从性的数字工具。
    The majority of Black women with hypertension in the United States have smartphones or tablets and use social media, and many use wearable activity trackers and health or wellness apps, digital tools that can be used to support lifestyle changes and medication adherence.
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  • 文章类型: Journal Article
    传感器技术可以提供解决方案来监测姿势和动作,并帮助医院患者在最少的监督下实现康复目标。缺乏有关设备应用和方法的综合信息。
    本次范围审查的目的是提供使用传感器技术监测住院患者姿势和运动的设备应用和方法学方法的概述。
    对Embase的系统搜索,Medline,WebofScience和GoogleScholar于2023年2月完成,并于2024年3月更新。纳入的研究描述了入院时间短的住院成年人人群,以及使用传感器技术客观监测姿势和运动的干预措施。研究选择由两名作者彼此独立进行。数据提取和叙事分析侧重于使用个性化标准表格提取设备信息的应用和方法方法。纳入研究的测量和分析特征,分析频率和使用情况。
    共发现15.032篇文章,49篇文章符合纳入标准。设备最常见于老年人(n=14),等待或手术后的患者(n=14),和中风(n=6)。主要目标是深入了解患者的身体行为模式(n=19),并调查与其他参数(例如肌肉力量或住院时间)有关的身体行为(n=18)。这些研究具有不同的研究设计,并且在设备设置报告方面缺乏完整性,数据分析,和算法。有关设备设置的信息,数据分析,和算法的报道很少。
    关于监测姿势和动作的研究在其人群中是异质的,应用和方法论方法。方法和研究报告的更统一和透明度将提高可重复性,结果的解释和概括。报告以及收集和共享原始数据的明确准则将通过进行研究比较和复制而使该领域受益。
    在临床环境中,可穿戴设备目前用于监测各种研究应用和医院人群的姿势和动作。在医院环境中测量姿势和运动的特征在于方法上的异质性。这构成了重大挑战,影响结果的解释并阻碍研究之间有意义的比较遵循报告和收集和共享原始数据的指南将有利于该领域。
    UNASSIGNED: Sensor technology could provide solutions to monitor postures and motions and to help hospital patients reach their rehabilitation goals with minimal supervision. Synthesized information on device applications and methodology is lacking.
    UNASSIGNED: The purpose of this scoping review was to provide an overview of device applications and methodological approaches to monitor postures and motions in hospitalized patients using sensor technology.
    UNASSIGNED: A systematic search of Embase, Medline, Web of Science and Google Scholar was completed in February 2023 and updated in March 2024. Included studies described populations of hospitalized adults with short admission periods and interventions that use sensor technology to objectively monitor postures and motions. Study selection was performed by two authors independently of each other. Data extraction and narrative analysis focused on the applications and methodological approaches of included articles using a personalized standard form to extract information on device, measurement and analysis characteristics of included studies and analyse frequencies and usage.
    UNASSIGNED: A total of 15.032 articles were found and 49 articles met the inclusion criteria. Devices were most often applied in older adults (n = 14), patients awaiting or after surgery (n = 14), and stroke (n = 6). The main goals were gaining insight into patient physical behavioural patterns (n = 19) and investigating physical behaviour in relation to other parameters such as muscle strength or hospital length of stay (n = 18). The studies had heterogeneous study designs and lacked completeness in reporting on device settings, data analysis, and algorithms. Information on device settings, data analysis, and algorithms was poorly reported.
    UNASSIGNED: Studies on monitoring postures and motions are heterogeneous in their population, applications and methodological approaches. More uniformity and transparency in methodology and study reporting would improve reproducibility, interpretation and generalization of results. Clear guidelines for reporting and the collection and sharing of raw data would benefit the field by enabling study comparison and reproduction.
    In a clinical setting, wearables are currently used to monitor postures and motions in a wide variety of study applications and hospital populations.Measurement of postures and motions in the hospital setting is characterized by methodological heterogeneity. This poses a significant challenge, impacting the interpretation of results and hindering meaningful comparisons between studiesFollowing guidelines for reporting and the collection and sharing of raw data would benefit the field.
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  • 文章类型: Journal Article
    背景:可穿戴数字健康技术和移动应用程序(个人数字健康技术[DHT])为改变健康研究和护理提供了巨大的希望。然而,对个人DHT研究的参与度很差。
    目的:本文的目的是描述参与者参与技术和不同的研究设计如何影响参与者的依从性,保留,以及全面参与涉及个人DHT的研究。
    方法:在6个独特的个人DHT研究中报告了参与因素的定量和定性分析,这些研究采用了以参与者为中心的设计。研究人群包括(1)一线医护人员;(2)一个概念,怀孕,和产后人群;(3)克罗恩病个体;(4)胰腺癌个体;(5)中枢神经系统肿瘤个体;和(6)患有Li-Fraumeni综合征受影响成员的家庭。所有纳入的研究都涉及使用研究智能手机应用程序,该应用程序收集了日常和间歇性的被动和主动任务,以及使用包括智能手表在内的多种可穿戴设备,聪明的戒指,和智能秤。所有研究都包括各种以参与者为中心的参与策略,该策略以与参与者作为共同设计师和定期检查电话为中心,以提供对研究参与的支持。总体保留,留在研究中的可能性,报告了对研究活动的依从性中位数。
    结果:在6项研究中保留的参与者的中位数比例为77.2%(IQR72.6%-88%)。在研究参与的第一个月中,所有研究的停留在研究中的概率保持在80%以上,在所有研究的整个活跃研究期间保持在50%以上。对研究活动的依从性中位数因研究人群而异。严重癌症人群和产后母亲对个人DHT研究任务的依从性最低,很大程度上是身体的结果,心理,和情境障碍。除了癌症和产后人群,Oura智能戒指的中位数附着,Garmin,苹果智能手表的比例超过80%和90%,分别。除一个队列外,所有队列对预定入住电话的依从性中位数都很高(50%,IQR20%-75%:低参与度队列)。在这个低参与度队列中,对研究相关活动的依从性中位数低于所有其他纳入研究。
    结论:以参与者为中心的参与策略有助于在某些人群中保持参与者并保持良好的依从性。参与的主要障碍是参与者的负担(任务疲劳和不便),物理,心理,和情境障碍(无法完成任务),和低感知利益(缺乏对个人DHT价值的理解)。需要对个人DHT设计进行更多的特定人群定制,以便这些新工具可以被认为对最终用户具有个人价值。
    BACKGROUND: Wearable digital health technologies and mobile apps (personal digital health technologies [DHTs]) hold great promise for transforming health research and care. However, engagement in personal DHT research is poor.
    OBJECTIVE: The objective of this paper is to describe how participant engagement techniques and different study designs affect participant adherence, retention, and overall engagement in research involving personal DHTs.
    METHODS: Quantitative and qualitative analysis of engagement factors are reported across 6 unique personal DHT research studies that adopted aspects of a participant-centric design. Study populations included (1) frontline health care workers; (2) a conception, pregnant, and postpartum population; (3) individuals with Crohn disease; (4) individuals with pancreatic cancer; (5) individuals with central nervous system tumors; and (6) families with a Li-Fraumeni syndrome affected member. All included studies involved the use of a study smartphone app that collected both daily and intermittent passive and active tasks, as well as using multiple wearable devices including smartwatches, smart rings, and smart scales. All studies included a variety of participant-centric engagement strategies centered on working with participants as co-designers and regular check-in phone calls to provide support over study participation. Overall retention, probability of staying in the study, and median adherence to study activities are reported.
    RESULTS: The median proportion of participants retained in the study across the 6 studies was 77.2% (IQR 72.6%-88%). The probability of staying in the study stayed above 80% for all studies during the first month of study participation and stayed above 50% for the entire active study period across all studies. Median adherence to study activities varied by study population. Severely ill cancer populations and postpartum mothers showed the lowest adherence to personal DHT research tasks, largely the result of physical, mental, and situational barriers. Except for the cancer and postpartum populations, median adherences for the Oura smart ring, Garmin, and Apple smartwatches were over 80% and 90%, respectively. Median adherence to the scheduled check-in calls was high across all but one cohort (50%, IQR 20%-75%: low-engagement cohort). Median adherence to study-related activities in this low-engagement cohort was lower than in all other included studies.
    CONCLUSIONS: Participant-centric engagement strategies aid in participant retention and maintain good adherence in some populations. Primary barriers to engagement were participant burden (task fatigue and inconvenience), physical, mental, and situational barriers (unable to complete tasks), and low perceived benefit (lack of understanding of the value of personal DHTs). More population-specific tailoring of personal DHT designs is needed so that these new tools can be perceived as personally valuable to the end user.
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  • 文章类型: Journal Article
    背景:COVID-19大流行引发了各种遏制策略,例如在家工作政策和减少的社会接触,这极大地改变了人们的睡眠习惯。虽然以前的研究强调了这些限制对睡眠的负面影响,他们往往缺乏综合考虑其他因素的综合观点,如季节性变化和体力活动(PA),这也会影响睡眠。
    目的:本研究旨在使用重复问卷和可穿戴传感器的高分辨率被动测量相结合,纵向检查COVID-19大流行期间工作成年人睡眠模式的详细变化。我们调查睡眠和5组变量之间的关联:(1)人口统计学;(2)睡眠相关习惯;(3)PA行为;和外部因素,包括(4)大流行特定的限制和(5)研究期间的季节性变化。
    方法:我们在COVID-19大流行后期进行了一项为期1年的研究(2021年6月至2022年6月)。我们从参与者佩戴的健身追踪器收集了多传感器数据,以及通过每月问卷调查与工作和睡眠相关的措施。此外,我们在不同时间点使用芬兰的严格性指数来估计研究期间与大流行相关的封锁限制的程度.我们应用线性混合模型来检查大流行后期睡眠模式的变化及其与5组变量的关联。
    结果:分析了112名在职成年人27,350晚的睡眠模式。更严格的大流行措施与总睡眠时间(TST)增加(β=.003,95%CI0.001-0.005;P<.001)和睡眠中期(MS)延迟(β=.02,95%CI0.02-0.03;P<.001)相关。倾向于贪睡的个体在TST(β=.15,95%CI0.05-0.27;P=.006)和MS(β=.17,95%CI0.03-0.31;P=.01)方面均表现出更大的变异性。观察到睡眠模式的职业差异,服务人员经历较长的TST(β=0.37,95%CI0.14-0.61;P=.004)和较低的TST变异性(β=-.15,95%CI-0.27至-0.05;P<.001)。当天晚些时候参与PA与更长的TST相关(β=.03,95%CI0.02-0.04;P<.001)和更小的TST变异性(β=-.01,95%CI-0.02至0.00;P=.02)。较高的静息活动节律与较短的TST相关(β=-0.26,95%CI-0.29至-0.23;P<.001),早期MS(β=-0.29,95%CI-0.33至-0.26;P<.001),TST变异性降低(β=-0.16,95%CI-0.23至-0.09;P<.001)。
    结论:我们的研究提供了在大流行后期影响睡眠模式的因素的综合观点。当我们在大流行后驾驭未来的工作时,了解如何安排工作,生活方式的选择,和睡眠质量互动对于优化员工的福祉和绩效至关重要。
    BACKGROUND: The COVID-19 pandemic prompted various containment strategies, such as work-from-home policies and reduced social contact, which significantly altered people\'s sleep routines. While previous studies have highlighted the negative impacts of these restrictions on sleep, they often lack a comprehensive perspective that considers other factors, such as seasonal variations and physical activity (PA), which can also influence sleep.
    OBJECTIVE: This study aims to longitudinally examine the detailed changes in sleep patterns among working adults during the COVID-19 pandemic using a combination of repeated questionnaires and high-resolution passive measurements from wearable sensors. We investigate the association between sleep and 5 sets of variables: (1) demographics; (2) sleep-related habits; (3) PA behaviors; and external factors, including (4) pandemic-specific constraints and (5) seasonal variations during the study period.
    METHODS: We recruited working adults in Finland for a 1-year study (June 2021-June 2022) conducted during the late stage of the COVID-19 pandemic. We collected multisensor data from fitness trackers worn by participants, as well as work and sleep-related measures through monthly questionnaires. Additionally, we used the Stringency Index for Finland at various points in time to estimate the degree of pandemic-related lockdown restrictions during the study period. We applied linear mixed models to examine changes in sleep patterns during this late stage of the pandemic and their association with the 5 sets of variables.
    RESULTS: The sleep patterns of 27,350 nights from 112 working adults were analyzed. Stricter pandemic measures were associated with an increase in total sleep time (TST) (β=.003, 95% CI 0.001-0.005; P<.001) and a delay in midsleep (MS) (β=.02, 95% CI 0.02-0.03; P<.001). Individuals who tend to snooze exhibited greater variability in both TST (β=.15, 95% CI 0.05-0.27; P=.006) and MS (β=.17, 95% CI 0.03-0.31; P=.01). Occupational differences in sleep pattern were observed, with service staff experiencing longer TST (β=.37, 95% CI 0.14-0.61; P=.004) and lower variability in TST (β=-.15, 95% CI -0.27 to -0.05; P<.001). Engaging in PA later in the day was associated with longer TST (β=.03, 95% CI 0.02-0.04; P<.001) and less variability in TST (β=-.01, 95% CI -0.02 to 0.00; P=.02). Higher intradaily variability in rest activity rhythm was associated with shorter TST (β=-.26, 95% CI -0.29 to -0.23; P<.001), earlier MS (β=-.29, 95% CI -0.33 to -0.26; P<.001), and reduced variability in TST (β=-.16, 95% CI -0.23 to -0.09; P<.001).
    CONCLUSIONS: Our study provided a comprehensive view of the factors affecting sleep patterns during the late stage of the pandemic. As we navigate the future of work after the pandemic, understanding how work arrangements, lifestyle choices, and sleep quality interact will be crucial for optimizing well-being and performance in the workforce.
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  • 文章类型: Journal Article
    土著人民的健康计划最有效,可接受,当土著观点被优先考虑时,也是可持续的。Cdesign建立在土著人民的创造力和倾向于尝试新技术的基础上,并确保以文化安全和尊重的方式设计和实施研究。有限的研究集中在老年人作为数字健康的合作伙伴。没有研究关注老年人使用可穿戴设备进行心脏健康监测的可接受性和可行性。这项研究提供了对居住在偏远地区的≥55岁土著人民使用可穿戴设备(手表和贴片)检测心房颤动(AF)和高血压的可接受性和可行性的见解。
    这项混合方法研究是与新南威尔士州偏远地区的当地原住民控制健康服务局共同设计和实施的,澳大利亚。它包括积极参与和与参与者的共同设计。这项研究中使用的设备包括WithingsScan手表和Biobeat贴片。
    尽管具有挑战性的条件(>36°C)和可变的互联网连接,11名土著老年人在偏远地区参加了为期五天的可穿戴设备计划。与会者指出,使用数字医疗设备对于老年土著用户来说是可以接受和可行的。他们描述了高水平的舒适度,使用可穿戴设备(补丁和手表)检测AF时的安全性和便利性。他们是共同设计该计划的积极参与者。
    澳大利亚老年人有动力使用可穿戴式健康设备。他们热衷于参与共同设计创新的健康技术计划,以确保新的健康技术为土著人民所接受,并在偏远地区可行。
    UNASSIGNED: Health programs for Indigenous people are most effective, acceptable, and sustainable when Indigenous perspectives are prioritized. Codesign builds on Indigenous people\'s creativity and propensity to experiment with new technologies and ensures research is designed and implemented in a culturally safe and respectful manner. Limited research has focused on older Indigenous people as partners in digital health. No research has focused on the acceptability and feasibility of older Indigenous people using wearables for heart health monitoring. This study provides insights into the acceptability and feasibility for ≥55-year-old Indigenous people living in remote locations to use wearables (watches and patches) to detect atrial fibrillation (AF) and high blood pressure.
    UNASSIGNED: This mixed methods study was codesigned and coimplemented with the local Aboriginal Controlled Health Service in a remote area of New South Wales, Australia. It included active involvement and codesign with the participants. The devices used in this study included a Withings Scan watch and a Biobeat patch.
    UNASSIGNED: Despite challenging conditions (>36°C) and variable internet connectivity, 11 Indigenous older adults participated in a five-day wearables program in a remote location. Participants indicated that using digital health devices was acceptable and feasible for older Indigenous users. They described high levels of comfort, safety and convenience when using wearables (patches and watches) to detect AF. They were active participants in codesigning the program.
    UNASSIGNED: Older Indigenous Australians are motivated to use wearable health devices. They are keen to participate in codesign innovative health tech programs to ensure new health technologies are acceptable to Indigenous people and feasible for remote locations.
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  • 文章类型: Journal Article
    背景:可穿戴活动跟踪器,包括健身带和智能手表,通过监测生理参数提供疾病检测的潜力。然而,它们作为特定疾病诊断工具的准确性仍然不确定。
    目的:本系统综述和荟萃分析旨在评估可穿戴活动跟踪器是否可用于检测疾病和医疗事件。
    方法:搜索了从开始到2023年4月1日发表的十个电子数据库。如果研究人员使用可穿戴活动跟踪器来诊断或检测医疗状况或事件(例如,跌倒)在成年人的自由生活条件下。进行荟萃分析以评估曲线下的总面积(%),准确度(%),灵敏度(%),特异性(%),和阳性预测值(%)。进行亚组分析以评估设备类型(Fitbit,Oura戒指,和混合)。使用JoannaBriggs研究所诊断测试准确性研究关键评估清单评估偏倚风险。
    结果:共纳入28项研究,共涉及1,226,801名参与者(年龄范围28.6-78.3)。总的来说,16项(57%)研究使用可穿戴设备诊断COVID-19,5项(18%)研究用于房颤,3(11%)心律失常或异常脉搏的研究,3(11%)的跌倒研究,和1(4%)的病毒症状研究。使用的设备是Fitbit(n=6),苹果手表(n=6),Oura环(n=3),设备的组合(n=7),EmpaticaE4(n=1),DynaportMoveMonitor(n=2),三星Galaxy手表(n=1),和其他或未指定(n=2)。对于COVID-19检测,荟萃分析显示,曲线下的合并面积为80.2%(95%CI71.0%-89.3%),准确率为87.5%(95%CI81.6%-93.5%),灵敏度为79.5%(95%CI67.7%-91.3%),特异性为76.8%(95%CI69.4%-84.1%)。对于心房颤动检测,合并阳性预测值为87.4%(95%CI75.7%-99.1%),灵敏度为94.2%(95%CI88.7%-99.7%),特异性为95.3%(95%CI91.8%-98.8%)。对于跌倒检测,合并敏感性为81.9%(95%CI75.1%-88.1%),特异性为62.5%(95%CI14.4%-100%).
    结论:可穿戴活动跟踪器在疾病检测中显示出希望,在识别心房颤动和COVID-19方面具有显著的准确性。虽然这些发现令人鼓舞,需要进一步的研究和改进,以提高其诊断精度和适用性。
    背景:ProsperoCRD42023407867;https://www.crd.约克。AC.uk/prospro/display_record.php?RecordID=407867。
    BACKGROUND: Wearable activity trackers, including fitness bands and smartwatches, offer the potential for disease detection by monitoring physiological parameters. However, their accuracy as specific disease diagnostic tools remains uncertain.
    OBJECTIVE: This systematic review and meta-analysis aims to evaluate whether wearable activity trackers can be used to detect disease and medical events.
    METHODS: Ten electronic databases were searched for studies published from inception to April 1, 2023. Studies were eligible if they used a wearable activity tracker to diagnose or detect a medical condition or event (eg, falls) in free-living conditions in adults. Meta-analyses were performed to assess the overall area under the curve (%), accuracy (%), sensitivity (%), specificity (%), and positive predictive value (%). Subgroup analyses were performed to assess device type (Fitbit, Oura ring, and mixed). The risk of bias was assessed using the Joanna Briggs Institute Critical Appraisal Checklist for Diagnostic Test Accuracy Studies.
    RESULTS: A total of 28 studies were included, involving a total of 1,226,801 participants (age range 28.6-78.3). In total, 16 (57%) studies used wearables for diagnosis of COVID-19, 5 (18%) studies for atrial fibrillation, 3 (11%) studies for arrhythmia or abnormal pulse, 3 (11%) studies for falls, and 1 (4%) study for viral symptoms. The devices used were Fitbit (n=6), Apple watch (n=6), Oura ring (n=3), a combination of devices (n=7), Empatica E4 (n=1), Dynaport MoveMonitor (n=2), Samsung Galaxy Watch (n=1), and other or not specified (n=2). For COVID-19 detection, meta-analyses showed a pooled area under the curve of 80.2% (95% CI 71.0%-89.3%), an accuracy of 87.5% (95% CI 81.6%-93.5%), a sensitivity of 79.5% (95% CI 67.7%-91.3%), and specificity of 76.8% (95% CI 69.4%-84.1%). For atrial fibrillation detection, pooled positive predictive value was 87.4% (95% CI 75.7%-99.1%), sensitivity was 94.2% (95% CI 88.7%-99.7%), and specificity was 95.3% (95% CI 91.8%-98.8%). For fall detection, pooled sensitivity was 81.9% (95% CI 75.1%-88.1%) and specificity was 62.5% (95% CI 14.4%-100%).
    CONCLUSIONS: Wearable activity trackers show promise in disease detection, with notable accuracy in identifying atrial fibrillation and COVID-19. While these findings are encouraging, further research and improvements are required to enhance their diagnostic precision and applicability.
    BACKGROUND: Prospero CRD42023407867; https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=407867.
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  • 文章类型: Journal Article
    2型糖尿病发病率的上升强调了技术创新的必要性,旨在通过帮助个人监测他们的饮食摄入量来加强糖尿病管理。这导致了能够跟踪个人进餐的时间和内容的技术的发展。然而,使用非侵入性可穿戴设备来估计或分类个体刚刚食用的食物中的碳水化合物含量的能力仍然是一个相对未探索的领域。本研究使用非侵入性可穿戴设备的餐后心率反应调查碳水化合物含量分类。我们设计并开发了timeStampr,一个iOS应用程序,用于收集数据标记和建立地面实况所必需的时间戳。然后,我们进行了一项对照试验研究,然而自然主义的设置。使用佩戴在上臂上的EmpaticaE4设备从23名参与者收集数据。而每个参与者都食用低碳水化合物或富含碳水化合物的食物。由于传感器的不规则性与暗肤色和不符合研究的健康标准,我们排除了3名参与者的数据.最后,我们配置并训练了用于碳水化合物含量分类的光梯度提升机(LGBM)模型。我们的分类器表现出强大的性能,碳水化合物含量分类模型始终达到至少84%的准确率,精度,召回,和AUCROC在60s窗口内。这项研究的结果证明了非侵入性可穿戴设备在碳水化合物含量分类中的餐后心率反应的潜力。
    The rising incidence of type 2 diabetes underscores the need for technological innovations aimed at enhancing diabetes management by aiding individuals in monitoring their dietary intake. This has resulted in the development of technologies capable of tracking the timing and content of an individual\'s meals. However, the ability to use non-invasive wearables to estimate or classify the carbohydrate content of the food an individual has just consumed remains a relatively unexplored area. This study investigates carbohydrate content classification using postprandial heart rate responses from non-invasive wearables. We designed and developed timeStampr, an iOS application for collecting timestamps essential for data labeling and establishing ground truth. We then conducted a pilot study in controlled, yet naturalistic settings. Data were collected from 23 participants using an Empatica E4 device worn on the upper arm, while each participant consumed either low-carbohydrate or carbohydrate-rich foods. Due to sensor irregularities with dark skin tones and non-compliance with the study\'s health criteria, we excluded data from three participants. Finally, we configured and trained a Light Gradient Boosting Machine (LGBM) model for carbohydrate content classification. Our classifiers demonstrated robust performance, with the carbohydrate content classification model consistently achieving at least 84% in accuracy, precision, recall, and AUCROC within a 60 s window. The results of this study demonstrate the potential of postprandial heart rate responses from non-invasive wearables in carbohydrate content classification.
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  • 文章类型: Journal Article
    背景:生命体征的纵向监测提供了一种识别个体总体健康状况变化的方法,尤其是老年人。夜间睡眠期提供了评估生命体征的便利机会。可以嵌入到卧室环境中的非接触式技术是非侵入性和无负担的,并且有可能实现生命体征的无缝监测。为了实现这种潜力,这些技术需要根据黄金标准措施和相关人群进行评估。
    目的:我们旨在评估3种非接触式技术(2种床下跟踪器,Withings睡眠分析仪[WSA]和EmfitQS[Emfit];以及床边雷达,Somnofy)在睡眠实验室环境中,并评估其在现实世界中捕获生命体征的潜力。
    方法:在睡眠实验室进行的1晚临床多导睡眠图(PSG)测试中,收集了35名社区居住的65至83岁(平均70.8,SD4.9)岁的老年人(男性:n=21,60%)的数据。之前是在家收集7到14天的数据。一些参与者(20/35,57%)有健康状况,包括2型糖尿病,高血压,肥胖,和关节炎,49%(17)患有中度至重度睡眠呼吸暂停,29%(n=10)有周期性腿部运动障碍。床垫下跟踪器提供了心率和呼吸率的估计值,而床边雷达只提供呼吸频率。将设备估计的心率和呼吸频率的准确性与PSG心电图得出的心率(每分钟心跳数)和呼吸电感体积描记术得出的呼吸频率(每分钟循环数)进行比较,分别。我们还评估了打鼾的呼吸干扰指数和呼吸暂停低通气指数。可从WSA获得。
    结果:所有3种非接触式技术在1分钟分辨率下估计心率(平均绝对误差<每分钟2.12次,平均绝对百分比误差<5%)和呼吸率(平均绝对误差≤每分钟1.6个周期,平均绝对百分比误差<12%)方面均提供了可接受的准确性。所有3种非接触式技术都能够捕获整个睡眠期间心率和呼吸频率的变化。与PSG估计相比,WSA打鼾和呼吸干扰估计也是准确的(WSA打鼾:r2=0.76;P<.001;WSA呼吸暂停低通气指数:r2=0.59;P<.001)。
    结论:非接触式技术提供了传统可穿戴技术的非侵入性替代方案,用于可靠地监测心率,呼吸频率,社区居住老年人的睡眠呼吸暂停。它们能够评估这些生命体征的夜间变化,这可以识别健康的急性变化,和纵向监测,这可以提供对健康轨迹的洞察。
    RR2-10.3390/clockssssleep6010010.
    BACKGROUND: Longitudinal monitoring of vital signs provides a method for identifying changes to general health in an individual, particularly in older adults. The nocturnal sleep period provides a convenient opportunity to assess vital signs. Contactless technologies that can be embedded into the bedroom environment are unintrusive and burdenless and have the potential to enable seamless monitoring of vital signs. To realize this potential, these technologies need to be evaluated against gold standard measures and in relevant populations.
    OBJECTIVE: We aimed to evaluate the accuracy of heart rate and breathing rate measurements of 3 contactless technologies (2 undermattress trackers, Withings Sleep Analyzer [WSA] and Emfit QS [Emfit]; and a bedside radar, Somnofy) in a sleep laboratory environment and assess their potential to capture vital signs in a real-world setting.
    METHODS: Data were collected from 35 community-dwelling older adults aged between 65 and 83 (mean 70.8, SD 4.9) years (men: n=21, 60%) during a 1-night clinical polysomnography (PSG) test in a sleep laboratory, preceded by 7 to 14 days of data collection at home. Several of the participants (20/35, 57%) had health conditions, including type 2 diabetes, hypertension, obesity, and arthritis, and 49% (17) had moderate to severe sleep apnea, while 29% (n=10) had periodic leg movement disorder. The undermattress trackers provided estimates of both heart rate and breathing rate, while the bedside radar provided only the breathing rate. The accuracy of the heart rate and breathing rate estimated by the devices was compared with PSG electrocardiogram-derived heart rate (beats per minute) and respiratory inductance plethysmography thorax-derived breathing rate (cycles per minute), respectively. We also evaluated breathing disturbance indexes of snoring and the apnea-hypopnea index, available from the WSA.
    RESULTS: All 3 contactless technologies provided acceptable accuracy in estimating heart rate (mean absolute error <2.12 beats per minute and mean absolute percentage error <5%) and breathing rate (mean absolute error ≤1.6 cycles per minute and mean absolute percentage error <12%) at 1-minute resolution. All 3 contactless technologies were able to capture changes in heart rate and breathing rate across the sleep period. The WSA snoring and breathing disturbance estimates were also accurate compared with PSG estimates (WSA snore: r2=0.76; P<.001; WSA apnea-hypopnea index: r2=0.59; P<.001).
    CONCLUSIONS: Contactless technologies offer an unintrusive alternative to conventional wearable technologies for reliable monitoring of heart rate, breathing rate, and sleep apnea in community-dwelling older adults at scale. They enable the assessment of night-to-night variation in these vital signs, which may allow the identification of acute changes in health, and longitudinal monitoring, which may provide insight into health trajectories.
    UNASSIGNED: RR2-10.3390/clockssleep6010010.
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  • 文章类型: Journal Article
    由于其固有的合规性,软机器人技术的最新进展已成为工程中令人兴奋的范例,安全的人类互动,和易于适应可穿戴电子产品。软机器人设备有可能提供创新的解决方案,并通过使机器人更接近自然生物来扩大生物医学应用的可能性。在这次审查中,我们调查了几种有前途的软机器人技术,包括柔性流体致动器,形状记忆合金,电缆驱动机构,磁力驱动机构,软传感器。讨论了软机器人设备作为医疗设备的选定应用,比如手术干预,软植入物,康复和辅助设备,软机器人机械护甲,和假肢。我们专注于软机器人如何提高效率,每个用例的安全性和患者体验,并强调当前的研究和临床挑战,如生物相容性,长期稳定,和耐用性。最后,我们讨论了解决这些挑战的潜在方向和方法,为未来的软机器人设备走向真正的临床翻译。
    Recent advancements in soft robotics have been emerging as an exciting paradigm in engineering due to their inherent compliance, safe human interaction, and ease of adaptation with wearable electronics. Soft robotic devices have the potential to provide innovative solutions and expand the horizons of possibilities for biomedical applications by bringing robots closer to natural creatures. In this review, we survey several promising soft robot technologies, including flexible fluidic actuators, shape memory alloys, cable-driven mechanisms, magnetically driven mechanisms, and soft sensors. Selected applications of soft robotic devices as medical devices are discussed, such as surgical intervention, soft implants, rehabilitation and assistive devices, soft robotic exosuits, and prosthetics. We focus on how soft robotics can improve the effectiveness, safety and patient experience for each use case, and highlight current research and clinical challenges, such as biocompatibility, long-term stability, and durability. Finally, we discuss potential directions and approaches to address these challenges for soft robotic devices to move toward real clinical translations in the future.
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