Validation of a Wearable Sensor Prototype for Measuring Heart Rate to Prescribe Physical Activity: Cross-Sectional Exploratory Study.

Fernanda Laís Loro, Riane Martins, Janaína Barcellos Ferreira, Cintia Laura Pereira de Araujo, Lucio Rene Prade, Cristiano Bonato Both, Jéferson Campos Nobre Nobre, Mariane Borba Monteiro, Pedro Dal Lago
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Abstract

Background: Wearable sensors are rapidly evolving, particularly in health care, due to their ability to facilitate continuous or on-demand physiological monitoring.

Objective: This study aimed to design and validate a wearable sensor prototype incorporating photoplethysmography (PPG) and long-range wide area network technology for heart rate (HR) measurement during a functional test.

Methods: We conducted a transversal exploratory study involving 20 healthy participants aged between 20 and 30 years without contraindications for physical exercise. Initially, our laboratory developed a pulse wearable sensor prototype for HR monitoring. Following this, the participants were instructed to perform the Incremental Shuttle Walk Test while wearing the Polar H10 HR chest strap sensor (the reference for HR measurement) and the wearable sensor. This test allowed for real-time comparison of HR responses between the 2 devices. Agreement between these measurements was determined using the intraclass correlation coefficient (ICC3.1) and Lin concordance correlation coefficient. The mean absolute percentage error was calculated to evaluate reliability or validity. Cohen d was used to calculate the agreement's effect size.

Results: The mean differences between the Polar H10 and the wearable sensor during the test were -2.6 (95% CI -3.5 to -1.8) for rest HR, -4.1 (95% CI -5.3 to -3) for maximum HR, -2.4 (95% CI -3.5 to -1.4) for mean test HR, and -2.5 (95% CI -3.6 to -1.5) for mean recovery HR. The mean absolute percentage errors were -3% for rest HR, -2.2% for maximum HR, -1.8% for mean test HR, and -1.6% for recovery HR. Excellent agreement was observed between the Polar H10 and the wearable sensor for rest HR (ICC3.1=0.96), mean test HR (ICC3.1=0.92), and mean recovery HR (ICC3.1=0.96). The agreement for maximum HR (ICC3.1=0.78) was considered good. By the Lin concordance correlation coefficient, the agreement was found to be substantial for rest HR (rc=0.96) and recovery HR (rc=0.96), moderate for mean test HR (rc=0.92), and poor for maximum HR (rc=0.78). The power of agreement between the Polar H10 and the wearable sensor prototype was large for baseline HR (Cohen d=0.97), maximum HR (Cohen d=1.18), and mean recovery HR (Cohen d=0.8) and medium for mean test HR (Cohen d= 0.76).

Conclusions: The pulse-wearable sensor prototype tested in this study proves to be a valid tool for monitoring HR at rest, during functional tests, and during recovery compared with the Polar H10 reference device used in the laboratory setting.

用于测量心率以规定体力活动的可穿戴传感器原型的验证:横断面探索性研究。
背景:可穿戴传感器正在迅速发展,特别是在医疗保健领域,因为它们能够促进连续或按需生理监测。目的:本研究旨在设计并验证一种结合光电容积脉搏波(PPG)和远程广域网技术的可穿戴传感器原型,用于在功能测试中测量心率(HR)。方法:我们进行了一项横向探索性研究,涉及20名年龄在20至30岁之间无体育锻炼禁忌症的健康参与者。最初,我们的实验室开发了一个脉搏可穿戴传感器原型用于HR监测。在此之后,参与者被指示在佩戴Polar H10 HR胸带传感器(HR测量参考)和可穿戴传感器的情况下进行增量穿梭行走测试。该测试允许实时比较两个设备之间的HR响应。使用类内相关系数(ICC3.1)和Lin一致性相关系数来确定这些测量之间的一致性。计算平均绝对误差百分比以评估信度或效度。Cohen被用来计算协议的效应大小。结果:Polar H10和可穿戴传感器在测试期间的平均差异为休息HR -2.6 (95% CI -3.5至-1.8),最大HR -4.1 (95% CI -5.3至-3),平均测试HR -2.4 (95% CI -3.5至-1.4),平均恢复HR -2.5 (95% CI -3.6至-1.5)。休息HR的平均绝对百分比误差为-3%,最大HR为-2.2%,平均测试HR为-1.8%,恢复HR为-1.6%。Polar H10与可穿戴传感器在休息心率(ICC3.1=0.96)、平均测试心率(ICC3.1=0.92)和平均恢复心率(ICC3.1=0.96)方面表现出极好的一致性。最大HR (ICC3.1=0.78)一致性较好。通过Lin一致性相关系数,发现休息HR (rc=0.96)和恢复HR (rc=0.96)的一致性较高,平均检验HR (rc=0.92)的一致性中等,最大HR (rc=0.78)的一致性较差。Polar H10与可穿戴传感器样机的基线HR (Cohen d=0.97)、最大HR (Cohen d=1.18)和平均恢复HR (Cohen d=0.8)的一致性较大,平均测试HR (Cohen d= 0.76)的一致性中等。结论:与实验室中使用的Polar H10参考设备相比,本研究中测试的脉冲可穿戴传感器原型被证明是静止、功能测试和恢复期间监测HR的有效工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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