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Severity Classification Using Dynamic Time Warping-Based Voice Biomarkers for COVID-19 Infected Patients: A Feasibility Study (Preprint) 基于动态时间扭曲的语音生物标志物对COVID-19感染患者进行严重程度分类的可行性研究(预印本)
Pub Date : 2023-11-06 DOI: 10.2196/50924
Teruhisa Watase, Yasuhiro Omiya, Shinichi Tokuno
Background In Japan, individuals with mild COVID-19 illness previously required to be monitored in designated areas and were hospitalized only if their condition worsened to moderate illness or worse. Daily monitoring using a pulse oximeter was a crucial indicator for hospitalization. However, a drastic increase in the number of patients resulted in a shortage of pulse oximeters for monitoring. Therefore, an alternative and cost-effective method for monitoring patients with mild illness was required. Previous studies have shown that voice biomarkers for Parkinson disease or Alzheimer disease are useful for classifying or monitoring symptoms; thus, we tried to adapt voice biomarkers for classifying the severity of COVID-19 using a dynamic time warping (DTW) algorithm where voice wavelets can be treated as 2D features; the differences between wavelet features are calculated as scores. Objective This feasibility study aimed to test whether DTW-based indices can generate voice biomarkers for a binary classification model using COVID-19 patients’ voices to distinguish moderate illness from mild illness at a significant level. Methods We conducted a cross-sectional study using voice samples of COVID-19 patients. Three kinds of long vowels were processed into 10-cycle waveforms with standardized power and time axes. The DTW-based indices were generated by all pairs of waveforms and tested with the Mann-Whitney U test (α<.01) and verified with a linear discrimination analysis and confusion matrix to determine which indices were better for binary classification of disease severity. A binary classification model was generated based on a generalized linear model (GLM) using the most promising indices as predictors. The receiver operating characteristic curve/area under the curve (ROC/AUC) validated the model performance, and the confusion matrix calculated the model accuracy. Results Participants in this study (n=295) were infected with COVID-19 between June 2021 and March 2022, were aged 20 years or older, and recuperated in Kanagawa prefecture. Voice samples (n=110) were selected from the participants’ attribution matrix based on age group, sex, time of infection, and whether they had mild illness (n=61) or moderate illness (n=49). The DTW-based variance indices were found to be significant (P<.001, except for 1 of 6 indices), with a balanced accuracy in the range between 79% and 88.6% for the /a/, /e/, and /u/ vowel sounds. The GLM achieved a high balance accuracy of 86.3% (for /a/), 80.2% (for /e/), and 88% (for /u/) and ROC/AUC of 94.8% (95% CI 90.6%-94.8%) for /a/, 86.5% (95% CI 79.8%-86.5%) for /e/, and 95.6% (95% CI 92.1%-95.6%) for /u/. Conclusions The proposed model can be a voice biomarker for an alternative and cost-effective method of monitoring the progress of COVID-19 patients in care.
在日本,患有COVID-19轻度疾病的个人以前需要在指定区域进行监测,只有当病情恶化到中度或更严重时才需要住院治疗。脉搏血氧仪的日常监测是住院治疗的关键指标。然而,患者数量的急剧增加导致用于监测的脉搏血氧仪短缺。因此,需要一种具有成本效益的替代方法来监测轻度疾病患者。先前的研究表明,帕金森病或阿尔茨海默病的语音生物标志物有助于分类或监测症状;因此,我们尝试使用动态时间规整(DTW)算法调整语音生物标记物来分类COVID-19的严重程度,其中语音小波可以被视为2D特征;小波特征之间的差异被计算为分数。目的本可行性研究旨在检验基于dtw的指标能否生成语音生物标志物,用于基于COVID-19患者声音的二元分类模型,在显著水平上区分中度疾病和轻度疾病。方法采用新冠肺炎患者语音样本进行横断面研究。将三种长元音加工成具有标准化功率轴和时间轴的10周波形。基于dtw的指标由所有对波形生成,采用Mann-Whitney U检验(α<.01)进行检验,并采用线性判别分析和混淆矩阵进行验证,以确定哪些指标更适合疾病严重程度的二元分类。在广义线性模型(GLM)的基础上,以最有希望的指标作为预测因子,建立了二元分类模型。受试者工作特征曲线/曲线下面积(ROC/AUC)验证模型性能,混淆矩阵计算模型精度。结果本研究的参与者(n=295)于2021年6月至2022年3月期间感染COVID-19,年龄在20岁及以上,在神奈川县休养。根据参与者的年龄、性别、感染时间以及是否患有轻度疾病(n=61)或中度疾病(n=49),从他们的归因矩阵中选择语音样本(n=110)。基于dtw的方差指标显著(P<001, 6个指标中的1个除外),对于/a/, /e/和/u/元音的平衡准确率在79%到88.6%之间。GLM的平衡准确度为86.3% (/a/), 80.2% (/e/)和88% (/u/), /a/的ROC/AUC为94.8% (95% CI 90.6%-94.8%), /e/的86.5% (95% CI 79.8%-86.5%), /u/的95.6% (95% CI 92.1%-95.6%)。结论该模型可作为一种语音生物标志物,为监测COVID-19患者在护理中的进展提供一种替代且具有成本效益的方法。
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引用次数: 0
Continuous Critical Respiratory Parameter Measurements Using a Single Low-Cost Relative Humidity Sensor: Evaluation Study 使用单一低成本相对湿度传感器的连续关键呼吸参数测量:评估研究
Pub Date : 2023-10-25 DOI: 10.2196/47146
Fabrice Vaussenat, Abhiroop Bhattacharya, Julie Payette, Jaime A Benavides-Guerrero, Alexandre Perrotton, Luis Felipe Gerlein, Sylvain G Cloutier
Background Accurate and portable respiratory parameter measurements are critical for properly managing chronic obstructive pulmonary diseases (COPDs) such as asthma or sleep apnea, as well as controlling ventilation for patients in intensive care units, during surgical procedures, or when using a positive airway pressure device for sleep apnea. Objective The purpose of this research is to develop a new nonprescription portable measurement device that utilizes relative humidity sensors (RHS) to accurately measure key respiratory parameters at a cost that is approximately 10 times less than the industry standard. Methods We present the development, implementation, and assessment of a wearable respiratory measurement device using the commercial Bosch BME280 RHS. In the initial stage, the RHS was connected to the pneumotach (PNT) gold standard device via its external connector to gather breathing metrics. Data collection was facilitated using the Arduino platform with a Bluetooth Low Energy connection, and all measurements were taken in real time without any additional data processing. The device’s efficacy was tested with 7 participants (5 men and 2 women), all in good health. In the subsequent phase, we specifically focused on comparing breathing cycle and respiratory rate measurements and determining the tidal volume by calculating the region between inhalation and exhalation peaks. Each participant's data were recorded over a span of 15 minutes. After the experiment, detailed statistical analysis was conducted using ANOVA and Bland-Altman to examine the accuracy and efficiency of our wearable device compared with the traditional methods. Results The perfused air measured with the respiratory monitor enables clinicians to evaluate the absolute value of the tidal volume during ventilation of a patient. In contrast, directly connecting our RHS device to the surgical mask facilitates continuous lung volume monitoring. The results of the 1-way ANOVA showed high P values of .68 for respiratory volume and .89 for respiratory rate, which indicate that the group averages with the PNT standard are equivalent to those with our RHS platform, within the error margins of a typical instrument. Furthermore, analysis utilizing the Bland-Altman statistical method revealed a small bias of 0.03 with limits of agreement (LoAs) of –0.25 and 0.33. The RR bias was 0.018, and the LoAs were –1.89 and 1.89. Conclusions Based on the encouraging results, we conclude that our proposed design can be a viable, low-cost wearable medical device for pulmonary parametric measurement to prevent and predict the progression of pulmonary diseases. We believe that this will encourage the research community to investigate the application of RHS for monitoring the pulmonary health of individuals.
准确和便携式的呼吸参数测量对于正确管理慢性阻塞性肺疾病(COPDs),如哮喘或睡眠呼吸暂停,以及在重症监护病房、外科手术期间或在使用气道正压装置治疗睡眠呼吸暂停时控制通气至关重要。目的研制一种新型非处方便携式测量装置,该装置利用相对湿度传感器(RHS)精确测量关键呼吸参数,成本比行业标准低约10倍。我们提出了一种使用商用博世BME280 RHS的可穿戴呼吸测量设备的开发、实施和评估。在初始阶段,RHS通过外部连接器连接到呼吸机(PNT)金标准设备,以收集呼吸指标。数据收集使用Arduino平台与蓝牙低功耗连接,所有测量都是实时进行的,无需任何额外的数据处理。7名参与者(5名男性和2名女性)对该装置的功效进行了测试,他们都身体健康。在随后的阶段,我们特别关注呼吸周期和呼吸频率测量的比较,并通过计算吸入和呼出峰值之间的区域来确定潮气量。每个参与者的数据在15分钟内被记录下来。实验结束后,采用方差分析和Bland-Altman进行详细的统计分析,对比传统方法检验我们的可穿戴设备的准确性和效率。结果用呼吸监测仪测量的灌注空气使临床医生能够评估患者通气时潮气量的绝对值。相反,将我们的RHS设备直接连接到外科口罩上,便于连续监测肺容量。单因素方差分析的结果显示呼吸量的P值为0.68,呼吸频率的P值为0.89,这表明使用PNT标准的组平均值与使用RHS平台的组平均值相当,在典型仪器的误差范围内。此外,利用Bland-Altman统计方法进行的分析显示,偏差较小,为0.03,一致性限(LoAs)为-0.25和0.33。RR偏倚为0.018,loa分别为-1.89和1.89。基于这些令人鼓舞的结果,我们得出结论,我们提出的设计可以成为一种可行的,低成本的可穿戴医疗设备,用于肺部参数测量,以预防和预测肺部疾病的进展。我们相信,这将鼓励研究界研究RHS在监测个人肺部健康方面的应用。
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引用次数: 0
A Wearable Vibratory Device (The Emma Watch) to Address Action Tremor in Parkinson Disease: Pilot Feasibility Study. 一种可穿戴振动装置治疗帕金森氏症动作震颤的初步可行性研究(预印本)
Pub Date : 2023-10-23 DOI: 10.2196/40433
Alissa Pacheco, Tempest A van Schaik, Nadzeya Paleyes, Miguel Blacutt, Julio Vega, Abigail R Schreier, Haiyan Zhang, Chelsea Macpherson, Radhika Desai, Gavin Jancke, Lori Quinn

Background: Parkinson disease (PD) is a neurodegenerative disease that has a wide range of motor symptoms, such as tremor. Tremors are involuntary movements that occur in rhythmic oscillations and are typically categorized into rest tremor or action tremor. Action tremor occurs during voluntary movements and is a debilitating symptom of PD. As noninvasive interventions are limited, there is an ever-increasing need for an effective intervention for individuals experiencing action tremors. The Microsoft Emma Watch, a wristband with 5 vibrating motors, is a noninvasive, nonpharmaceutical intervention for tremor attenuation.

Objective: This pilot study investigated the use of the Emma Watch device to attenuate action tremor in people with PD.

Methods: The sample included 9 people with PD who were assessed on handwriting and hand function tasks performed on a digitized tablet. Tasks included drawing horizontal or vertical lines, tracing a star, spiral, writing "elelelel" in cursive, and printing a standardized sentence. Each task was completed 3 times with the Emma Watch programmed at different vibration intensities, which were counterbalanced: high intensity, low intensity (sham), and no vibration. Digital analysis from the tablet captured kinematic, dynamic, and spatial attributes of drawing and writing samples to calculate mathematical indices that quantify upper limb motor function. APDM Opal sensors (APDM Wearable Technologies) placed on both wrists were used to calculate metrics of acceleration and jerk. A questionnaire was provided to each participant after using the Emma Watch to gain a better understanding of their perspectives of using the device. In addition, drawings were compared to determine whether there were any visual differences between intensities.

Results: In total, 9 people with PD were tested: 4 males and 5 females with a mean age of 67 (SD 9.4) years. There were no differences between conditions in the outcomes of interest measured with the tablet (duration, mean velocity, number of peaks, pause time, and number of pauses). Visual differences were observed within a small subset of participants, some of whom reported perceived improvement. The majority of participants (8/9) reported the Emma Watch was comfortable, and no problems with the device were reported.

Conclusions: There were visually depicted and subjectively reported improvements in handwriting for a small subset of individuals. This pilot study was limited by a small sample size, and this should be taken into consideration with the interpretation of the quantitative results. Combining vibratory devices, such as the Emma Watch, with task specific training, or personalizing the frequency to one's individual tremor may be important steps to consider when evaluating the effect of vibratory devices on hand function or writing ability in future studies. While the E

背景:帕金森病(PD)是一种神经退行性疾病,具有广泛的运动症状,如震颤。震颤是一种不自主的运动,呈节律性振荡,通常分为静止性震颤和运动性震颤。动作性震颤发生在自主运动时,是一种使人衰弱的帕金森病症状。由于非侵入性干预措施有限,人们越来越需要为出现动作性震颤的患者提供有效的干预措施。微软Emma Watch是一款带有5个振动马达的腕带,是一种非侵入性、非药物性的震颤缓解干预措施:本试验研究调查了使用 Emma Watch 设备来减轻帕金森氏症患者动作性震颤的情况:样本包括 9 名患有帕金森氏症的患者,他们在数字化平板电脑上进行了手写和手部功能任务评估。任务包括画水平线或垂直线、描星、螺旋线、草书 "elelelel "和打印标准句子。每项任务均由 Emma Watch 在不同振动强度下编程完成 3 次,并进行平衡:高强度、低强度(假振动)和无振动。平板电脑的数字分析捕捉了绘画和书写样本的运动、动态和空间属性,从而计算出量化上肢运动功能的数学指数。放置在双手手腕上的 APDM Opal 传感器(APDM 可穿戴技术公司)用于计算加速度和挺举度指标。每位参与者在使用 Emma Watch 后都会收到一份调查问卷,以更好地了解他们对使用该设备的看法。此外,还对图画进行了比较,以确定不同强度之间是否存在视觉差异:共有 9 名帕金森氏症患者接受了测试,其中男性 4 人,女性 5 人,平均年龄 67 岁(标准差 9.4)。使用平板电脑测量的结果(持续时间、平均速度、峰值数量、暂停时间和暂停数量)在不同条件下没有差异。在一小部分参与者中观察到了视觉差异,其中一些人表示感觉到了改善。大多数参与者(8/9)表示 Emma Watch 佩戴舒适,没有人报告设备出现问题:结论:一小部分人的手写能力有了直观的改善,并有主观报告。这项试点研究由于样本量较小而受到限制,在解释定量结果时应考虑到这一点。在未来的研究中,评估振动设备对手部功能或书写能力的影响时,将 Emma Watch 等振动设备与特定任务训练相结合,或根据个人震颤情况个性化调节频率,可能是需要考虑的重要步骤。虽然 Emma Watch 有助于减轻动作性震颤,但作为一种独立的工具,它在改善精细动作或书写技能方面的功效仍有待证实。
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引用次数: 0
Development and Testing of a Data Capture Device for Use With Clinical Incentive Spirometers: Testing and Usability Study. 激励肺活量计:创建和测试用于临床激励肺活计的数据采集设备。(预印本)
Pub Date : 2023-09-07 DOI: 10.2196/46653
Michael L Burns, Anik Sinha, Alexander Hoffmann, Zewen Wu, Tomas Medina Inchauste, Aaron Retsky, David Chesney, Sachin Kheterpal, Nirav Shah

Background: The incentive spirometer is a basic and common medical device from which electronic health care data cannot be directly collected. As a result, despite numerous studies investigating clinical use, there remains little consensus on optimal device use and sparse evidence supporting its intended benefits such as prevention of postoperative respiratory complications.

Objective: The aim of the study is to develop and test an add-on hardware device for data capture of the incentive spirometer.

Methods: An add-on device was designed, built, and tested using reflective optical sensors to identify the real-time location of the volume piston and flow bobbin of a common incentive spirometer. Investigators manually tested sensor level accuracies and triggering range calibrations using a digital flowmeter. A valid breath classification algorithm was created and tested to determine valid from invalid breath attempts. To assess real-time use, a video game was developed using the incentive spirometer and add-on device as a controller using the Apple iPad.

Results: In user testing, sensor locations were captured at an accuracy of 99% (SD 1.4%) for volume and 100% accuracy for flow. Median and average volumes were within 7.5% (SD 6%) of target volume sensor levels, and maximum sensor triggering values seldom exceeded intended sensor levels, showing a good correlation to placement on 2 similar but distinct incentive spirometer designs. The breath classification algorithm displayed a 100% sensitivity and a 99% specificity on user testing, and the device operated as a video game controller in real time without noticeable interference or delay.

Conclusions: An effective and reusable add-on device for the incentive spirometer was created to allow the collection of previously inaccessible incentive spirometer data and demonstrate Internet-of-Things use on a common hospital device. This design showed high sensor accuracies and the ability to use data in real-time applications, showing promise in the ability to capture currently inaccessible clinical data. Further use of this device could facilitate improved research into the incentive spirometer to improve adoption, incentivize adherence, and investigate the clinical effectiveness to help guide clinical care.

背景:激励肺活量计是一种基本且常见的医疗设备,无法直接收集电子医疗数据。因此,尽管有许多研究调查了该设备的临床使用情况,但对其最佳使用方法仍未达成共识,而且支持其预期益处(如预防术后呼吸系统并发症)的证据也很少:本研究的目的是开发和测试一种附加硬件设备,用于采集激励式肺活量计的数据:方法: 使用反射式光学传感器设计、制造和测试了一种附加装置,用于识别普通激励式肺活量计的体积活塞和流量线圈的实时位置。研究人员使用数字流量计手动测试了传感器水平精度和触发范围校准。创建并测试了有效呼吸分类算法,以确定有效和无效的呼吸尝试。为了评估实时使用情况,研究人员使用激励式肺活量计和附加装置开发了一款视频游戏,并将其作为使用苹果 iPad 的控制器:结果:在用户测试中,传感器位置捕捉的准确率为 99%(SD 1.4%),流量捕捉的准确率为 100%。中位数和平均体积在目标体积传感器水平的 7.5%(标准差 6%)以内,最大传感器触发值很少超过预期传感器水平,显示出与两个相似但不同的激励式肺活量计的位置有很好的相关性。在用户测试中,呼吸分类算法的灵敏度为 100%,特异性为 99%,该设备可以像视频游戏控制器一样实时运行,没有明显的干扰或延迟:我们为激励式肺活量计设计了一种有效且可重复使用的附加设备,以便收集以前无法获得的激励式肺活量计数据,并展示了在普通医院设备上使用物联网的情况。该设计显示了传感器的高精确度和在实时应用中使用数据的能力,显示了采集目前无法获取的临床数据的能力。该设备的进一步使用可促进对激励式肺活量计的研究,从而提高其采用率,激励人们坚持使用,并调查其临床效果,以帮助指导临床护理。
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引用次数: 0
Radar-Based Opioid Overdose Detection Device for Public Restrooms: Design, Development, and Evaluation (Preprint) 基于雷达的公共厕所阿片类药物过量检测装置:设计、开发和评估(预印本)
Pub Date : 2023-08-11 DOI: 10.2196/51754
Jessica Oreskovic, Jaycee Kaufman, Anirudh Thommandram, Yan Fossat
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引用次数: 0
The Variability of Lumbar Sequential Motion Patterns: Observational Study. 腰椎顺序运动模式的变异性:观察研究
Pub Date : 2023-06-20 DOI: 10.2196/41906
Inge Caelers, Toon Boselie, Wouter van Hemert, Kim Rijkers, Rob De Bie, Henk van Santbrink

Background: Physiological motion of the lumbar spine is a topic of interest for musculoskeletal health care professionals since abnormal motion is believed to be related to lumbar complaints. Many researchers have described ranges of motion for the lumbar spine, but only few have mentioned specific motion patterns of each individual segment during flexion and extension, mostly comprising the sequence of segmental initiation in sagittal rotation. However, an adequate definition of physiological motion is still lacking. For the lower cervical spine, a consistent pattern of segmental contributions in a flexion-extension movement in young healthy individuals was described, resulting in a definition of physiological motion of the cervical spine.

Objective: This study aimed to define the lumbar spines' physiological motion pattern by determining the sequence of segmental contribution in sagittal rotation of each vertebra during maximum flexion and extension in healthy male participants.

Methods: Cinematographic recordings were performed twice in 11 healthy male participants, aged 18-25 years, without a history of spine problems, with a 2-week interval (time point T1 and T2). Image recognition software was used to identify specific patterns in the sequence of segmental contributions per individual by plotting segmental rotation of each individual segment against the cumulative rotation of segments L1 to S1. Intraindividual variability was determined by testing T1 against T2. Intraclass correlation coefficients were tested by reevaluation of 30 intervertebral sequences by a second researcher.

Results: No consistent pattern was found when studying the graphs of the cinematographic recordings during flexion. A much more consistent pattern was found during extension, especially in the last phase. It consisted of a peak in rotation in L3L4, followed by a peak in L2L3, and finally, in L1L2. This pattern was present in 71% (15/21) of all recordings; 64% (7/11) of the participants had a consistent pattern at both time points. Sequence of segmental contribution was less consistent in the lumbar spine than the cervical spine, possibly caused by differences in facet orientation, intervertebral discs, overprojection of the pelvis, and muscle recruitment.

Conclusions: In 64% (7/11) of the recordings, a consistent motion pattern was found in the upper lumbar spine during the last phase of extension in asymptomatic young male participants. Physiological motion of the lumbar spine is a broad concept, influenced by multiple factors, which cannot be captured in a firm definition yet.

Trial registration: ClinicalTrials.gov NCT03737227; https://clinicaltrials.gov/ct2/show/NCT03737227.

International registered report identifier (irrid): RR2-10.2196/14741.

腰椎的生理运动是肌肉骨骼保健专业人员感兴趣的话题,因为异常运动被认为与腰椎疾病有关。许多研究人员描述了腰椎的运动范围,但很少有人提到屈曲和伸展过程中每个节段的具体运动模式,主要包括矢状旋转中节段起始的顺序。然而,对生理运动仍然缺乏足够的定义。对于下颈椎,描述了年轻健康个体屈伸运动中节段贡献的一致模式,从而定义了颈椎的生理运动。本研究旨在通过确定健康男性参与者在最大屈伸过程中每个椎骨矢状旋转的节段贡献顺序来确定腰椎的生理运动模式。对11名18-25岁的健康男性参与者进行了两次电影记录,他们没有脊椎问题史,间隔2周(时间点T1和T2)。图像识别软件用于通过绘制每个单独片段的片段旋转相对于片段L1至S1的累积旋转来识别每个个体的片段贡献序列中的特定模式。通过测试T1与T2来确定个体内变异性。第二位研究人员通过重新评估30个椎间盘序列来测试组内相关系数。在研究屈曲过程中的电影摄影记录图时,没有发现一致的模式。在扩展过程中发现了更加一致的模式,尤其是在最后一个阶段。它包括L3L4中的旋转峰值,然后是L2L3中的峰值,最后是L1L2中的峰值。这种模式出现在71%(15/21)的所有记录中;64%(7/11)的参与者在两个时间点都有一致的模式。腰椎节段贡献的顺序不如颈椎一致,这可能是由于小关节方向、椎间盘、骨盆过度投射和肌肉募集的差异造成的。在64%(7/11)的记录中,在无症状的年轻男性参与者的最后一个伸展阶段,在上腰椎发现了一致的运动模式。腰椎的生理运动是一个广泛的概念,受到多种因素的影响,目前还不能确定其定义。ClinicalTrials.gov NCT03737227;https://clinicaltrials.gov/ct2/show/NCT03737227RR2-10.2196/14471
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引用次数: 0
Mixed Reality Platforms in Telehealth Delivery: Scoping Review. 远程医疗服务中的混合现实平台:范围审查(预印本)
Pub Date : 2023-03-24 DOI: 10.2196/42709
Hemendra Worlikar, Sean Coleman, Jack Kelly, Sadhbh O'Connor, Aoife Murray, Terri McVeigh, Jennifer Doran, Ian McCabe, Derek O'Keeffe
<p><strong>Background: </strong>The distinctive features of the digital reality platforms, namely augmented reality (AR), virtual reality (VR), and mixed reality (MR) have extended to medical education, training, simulation, and patient care. Furthermore, this digital reality technology seamlessly merges with information and communication technology creating an enriched telehealth ecosystem. This review provides a composite overview of the prospects of telehealth delivered using the MR platform in clinical settings.</p><p><strong>Objective: </strong>This review identifies various clinical applications of high-fidelity digital display technology, namely AR, VR, and MR, delivered using telehealth capabilities. Next, the review focuses on the technical characteristics, hardware, and software technologies used in the composition of AR, VR, and MR in telehealth.</p><p><strong>Methods: </strong>We conducted a scoping review using the methodological framework and reporting design using the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses Extension for Scoping Reviews) guidelines. Full-length articles in English were obtained from the Embase, PubMed, and Web of Science databases. The search protocol was based on the following keywords and Medical Subject Headings to obtain relevant results: "augmented reality," "virtual reality," "mixed-reality," "telemedicine," "telehealth," and "digital health." A predefined inclusion-exclusion criterion was developed in filtering the obtained results and the final selection of the articles, followed by data extraction and construction of the review.</p><p><strong>Results: </strong>We identified 4407 articles, of which 320 were eligible for full-text screening. A total of 134 full-text articles were included in the review. Telerehabilitation, telementoring, teleconsultation, telemonitoring, telepsychiatry, telesurgery, and telediagnosis were the segments of the telehealth division that explored the use of AR, VR, and MR platforms. Telerehabilitation using VR was the most commonly recurring segment in the included studies. AR and MR has been mainly used for telementoring and teleconsultation. The most important technical features of digital reality technology to emerge with telehealth were virtual environment, exergaming, 3D avatars, telepresence, anchoring annotations, and first-person viewpoint. Different arrangements of technology-3D modeling and viewing tools, communication and streaming platforms, file transfer and sharing platforms, sensors, high-fidelity displays, and controllers-formed the basis of most systems.</p><p><strong>Conclusions: </strong>This review constitutes a recent overview of the evolving digital AR and VR in various clinical applications using the telehealth setup. This combination of telehealth with AR, VR, and MR allows for remote facilitation of clinical expertise and further development of home-based treatment. This review explores the rapidly growing suite of t
背景:数字现实平台的鲜明特征,即增强现实(AR)、虚拟现实(VR)
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引用次数: 0
An Algorithm to Classify Real-World Ambulatory Status From a Wearable Device Using Multimodal and Demographically Diverse Data: Validation Study. 使用多模式和人口学多样性数据对可穿戴设备的真实世界动态状态进行分类的算法的验证研究(预印本)
Pub Date : 2023-03-07 DOI: 10.2196/43726
Sara Popham, Maximilien Burq, Erin E Rainaldi, Sooyoon Shin, Jessilyn Dunn, Ritu Kapur

Background: Measuring the amount of physical activity and its patterns using wearable sensor technology in real-world settings can provide critical insights into health status.

Objective: This study's aim was to develop and evaluate the analytical validity and transdemographic generalizability of an algorithm that classifies binary ambulatory status (yes or no) on the accelerometer signal from wrist-worn biometric monitoring technology.

Methods: Biometric monitoring technology algorithm validation traditionally relies on large numbers of self-reported labels or on periods of high-resolution monitoring with reference devices. We used both methods on data collected from 2 distinct studies for algorithm training and testing, one with precise ground-truth labels from a reference device (n=75) and the second with participant-reported ground-truth labels from a more diverse, larger sample (n=1691); in total, we collected data from 16.7 million 10-second epochs. We trained a neural network on a combined data set and measured performance in multiple held-out testing data sets, overall and in demographically stratified subgroups.

Results: The algorithm was accurate at classifying ambulatory status in 10-second epochs (area under the curve 0.938; 95% CI 0.921-0.958) and on daily aggregate metrics (daily mean absolute percentage error 18%; 95% CI 15%-20%) without significant performance differences across subgroups.

Conclusions: Our algorithm can accurately classify ambulatory status with a wrist-worn device in real-world settings with generalizability across demographic subgroups. The validated algorithm can effectively quantify users' walking activity and help researchers gain insights on users' health status.

背景:利用可穿戴传感技术测量现实世界中的运动量及其模式,可以为了解健康状况提供重要依据:本研究旨在开发和评估一种算法的分析有效性和跨人口统计学的可推广性,该算法可根据腕戴式生物计量监测技术的加速度计信号对二元活动状态(是或否)进行分类:生物统计监测技术算法的验证传统上依赖于大量的自我报告标签或参考设备的高分辨率监测期。我们在两项不同研究中收集的数据上使用了这两种方法进行算法训练和测试,其中一项研究使用了来自参考设备的精确地面实况标签(n=75),另一项研究使用了来自更多样化、更大样本的参与者报告的地面实况标签(n=1691);我们总共收集了 1670 万个 10 秒历时的数据。我们在综合数据集上训练了一个神经网络,并在多个保留测试数据集上测量了整体和人口分层分组的性能:该算法能在 10 秒历时内准确地对非卧床状态进行分类(曲线下面积为 0.938;95% CI 为 0.921-0.958),在每日综合指标上也是如此(每日平均绝对百分比误差为 18%;95% CI 为 15%-20%),不同亚群之间没有明显的性能差异:我们的算法可以在真实世界环境中使用腕戴式设备准确地对非卧床状态进行分类,并具有跨人口亚群的普适性。经过验证的算法可以有效量化用户的步行活动,帮助研究人员深入了解用户的健康状况。
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引用次数: 0
Detection of Suicide Risk Using Vocal Characteristics: Systematic Review. 利用声音特征检测自杀风险:系统综述(预印本)
Pub Date : 2022-12-22 DOI: 10.2196/42386
Ravi Iyer, Denny Meyer

Background: In an age when telehealth services are increasingly being used for forward triage, there is a need for accurate suicide risk detection. Vocal characteristics analyzed using artificial intelligence are now proving capable of detecting suicide risk with accuracies superior to traditional survey-based approaches, suggesting an efficient and economical approach to ensuring ongoing patient safety.

Objective: This systematic review aimed to identify which vocal characteristics perform best at differentiating between patients with an elevated risk of suicide in comparison with other cohorts and identify the methodological specifications of the systems used to derive each feature and the accuracies of classification that result.

Methods: A search of MEDLINE via Ovid, Scopus, Computers and Applied Science Complete, CADTH, Web of Science, ProQuest Dissertations and Theses A&I, Australian Policy Online, and Mednar was conducted between 1995 and 2020 and updated in 2021. The inclusion criteria were human participants with no language, age, or setting restrictions applied; randomized controlled studies, observational cohort studies, and theses; studies that used some measure of vocal quality; and individuals assessed as being at high risk of suicide compared with other individuals at lower risk using a validated measure of suicide risk. Risk of bias was assessed using the Risk of Bias in Non-randomized Studies tool. A random-effects model meta-analysis was used wherever mean measures of vocal quality were reported.

Results: The search yielded 1074 unique citations, of which 30 (2.79%) were screened via full text. A total of 21 studies involving 1734 participants met all inclusion criteria. Most studies (15/21, 71%) sourced participants via either the Vanderbilt II database of recordings (8/21, 38%) or the Silverman and Silverman perceptual study recording database (7/21, 33%). Candidate vocal characteristics that performed best at differentiating between high risk of suicide and comparison cohorts included timing patterns of speech (median accuracy 95%), power spectral density sub-bands (median accuracy 90.3%), and mel-frequency cepstral coefficients (median accuracy 80%). A random-effects meta-analysis was used to compare 22 characteristics nested within 14% (3/21) of the studies, which demonstrated significant standardized mean differences for frequencies within the first and second formants (standardized mean difference ranged between -1.07 and -2.56) and jitter values (standardized mean difference=1.47). In 43% (9/21) of the studies, risk of bias was assessed as moderate, whereas in the remaining studies (12/21, 57%), the risk of bias was assessed as high.

Conclusions: Although several key methodological issues prevailed among the studies reviewed, there is promise in the use of vocal characteristics to detect elevations in suicide r

背景:在远程医疗服务越来越多地被用于前方分诊的时代,需要准确的自杀风险检测。使用人工智能分析的声音特征现在已被证明能够检测自杀风险,其准确性优于传统的基于调查的方法,这表明这是一种高效、经济的方法,可确保患者的持续安全:本系统综述旨在确定哪些声音特征在区分自杀风险较高的患者与其他人群方面表现最佳,并确定用于得出每个特征的系统的方法规范以及由此产生的分类准确性:1995年至2020年期间,通过Ovid、Scopus、Computers and Applied Science Complete、CADTH、Web of Science、ProQuest Dissertations and Theses A&I、Australian Policy Online和Mednar对MEDLINE进行了检索,并于2021年进行了更新。纳入标准包括:无语言、年龄或环境限制的人类参与者;随机对照研究、观察性队列研究和论文;使用某种声音质量测量方法的研究;使用有效的自杀风险测量方法将被评估为自杀风险较高的个体与自杀风险较低的其他个体进行比较。偏倚风险采用非随机研究中的偏倚风险工具进行评估。在报告声乐质量平均测量值的情况下,采用随机效应模型进行荟萃分析:搜索共获得 1074 条引文,其中 30 条(2.79%)通过全文筛选。共有 21 项研究(涉及 1734 名参与者)符合所有纳入标准。大多数研究(15/21,71%)通过范德比尔特 II 录音数据库(8/21,38%)或西尔弗曼和西尔弗曼知觉研究录音数据库(7/21,33%)寻找参与者。在区分自杀高危人群和对比人群方面表现最佳的候选声乐特征包括语音计时模式(中位数准确率为 95%)、功率谱密度子带(中位数准确率为 90.3%)和融频倒频系数(中位数准确率为 80%)。随机效应荟萃分析用于比较嵌套在 14% 的研究(3/21)中的 22 个特征,结果表明第一和第二前元音内的频率(标准化均值差异在-1.07 和-2.56 之间)和抖动值(标准化均值差异=1.47)具有显著的标准化均值差异。43%的研究(9/21)被评估为中度偏倚风险,而其余的研究(12/21,57%)被评估为高度偏倚风险:尽管所审查的研究普遍存在几个关键的方法问题,但使用声音特征检测自杀风险的升高是有希望的,尤其是在远程医疗或对话代理等新环境中:PROSPERO 国际前瞻性系统综述注册中心 CRD420200167413;https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42020167413。
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引用次数: 0
Detection of Mental Fatigue in the General Population: Feasibility Study of Keystroke Dynamics as a Real-world Biomarker. 普通人群精神疲劳的检测:击键动力学作为真实世界生物标志物的可行性研究
Pub Date : 2022-11-21 DOI: 10.2196/41003
Alejandro Acien, Aythami Morales, Ruben Vera-Rodriguez, Julian Fierrez, Ijah Mondesire-Crump, Teresa Arroyo-Gallego

Background: Mental fatigue is a common and potentially debilitating state that can affect individuals' health and quality of life. In some cases, its manifestation can precede or mask early signs of other serious mental or physiological conditions. Detecting and assessing mental fatigue can be challenging nowadays as it relies on self-evaluation and rating questionnaires, which are highly influenced by subjective bias. Introducing more objective, quantitative, and sensitive methods to characterize mental fatigue could be critical to improve its management and the understanding of its connection to other clinical conditions.

Objective: This paper aimed to study the feasibility of using keystroke biometrics for mental fatigue detection during natural typing. As typing involves multiple motor and cognitive processes that are affected by mental fatigue, our hypothesis was that the information captured in keystroke dynamics can offer an interesting mean to characterize users' mental fatigue in a real-world setting.

Methods: We apply domain transformation techniques to adapt and transform TypeNet, a state-of-the-art deep neural network, originally intended for user authentication, to generate a network optimized for the fatigue detection task. All experiments were conducted using 3 keystroke databases that comprise different contexts and data collection protocols.

Results: Our preliminary results showed area under the curve performances ranging between 72.2% and 80% for fatigue versus rested sample classification, which is aligned with previously published models on daily alertness and circadian cycles. This demonstrates the potential of our proposed system to characterize mental fatigue fluctuations via natural typing patterns. Finally, we studied the performance of an active detection approach that leverages the continuous nature of keystroke biometric patterns for the assessment of users' fatigue in real time.

Conclusions: Our results suggest that the psychomotor patterns that characterize mental fatigue manifest during natural typing, which can be quantified via automated analysis of users' daily interaction with their device. These findings represent a step towards the development of a more objective, accessible, and transparent solution to monitor mental fatigue in a real-world environment.

精神疲劳是一种常见的、可能使人衰弱的状态,会影响个人的健康和生活质量。在某些情况下,其表现可能先于或掩盖其他严重精神或生理状况的早期迹象。如今,检测和评估心理疲劳可能具有挑战性,因为它依赖于自我评价和评分问卷,而这些问卷深受主观偏见的影响。引入更客观、定量和敏感的方法来表征精神疲劳,对于改善其管理和理解其与其他临床状况的联系至关重要。本文旨在研究在自然打字过程中使用击键生物识别技术进行心理疲劳检测的可行性。由于打字涉及受心理疲劳影响的多个运动和认知过程,我们的假设是,在击键动力学中捕获的信息可以提供一种有趣的方法来描述用户在现实世界中的心理疲劳。我们应用域转换技术来调整和转换TypeNet,这是一种最先进的深度神经网络,最初用于用户身份验证,以生成一个针对疲劳检测任务优化的网络。所有实验都是使用3个击键数据库进行的,这些数据库包括不同的上下文和数据收集协议。我们的初步结果显示,疲劳与休息样本分类的曲线下面积表现在72.2%至80%之间,这与之前发表的每日警觉性和昼夜节律模型一致。这证明了我们提出的系统通过自然打字模式来表征精神疲劳波动的潜力。最后,我们研究了一种主动检测方法的性能,该方法利用击键生物特征模式的连续性来实时评估用户的疲劳程度。我们的研究结果表明,表征精神疲劳的心理运动模式在自然打字过程中表现出来,可以通过对用户与设备的日常互动进行自动分析来量化。这些发现代表着朝着开发一种更客观、可访问和透明的解决方案迈出了一步,该解决方案可在现实世界环境中监测心理疲劳。
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引用次数: 0
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