McClaine Sean, Fedor Jennifer, Bartel Christianna, Chen Leeann, Durica Krina C, Low Carissa A
University of Pittsburgh, Pittsburgh, PA, United States.
JMIR Cancer. 2024 Dec 10;10:e57347. doi: 10.2196/57347.
Chemotherapy can cause symptoms that impair quality of life and functioning. Remote monitoring of daily symptoms and activity during outpatient treatment may enable earlier detection and management of emerging toxicities but requires patients, including older and acutely ill patients, to engage with technology to report symptoms through smartphones and to charge and wear mobile devices.
This study aimed to identify factors associated with participant engagement with collecting 3 data streams (ie, daily patient-reported symptom surveys, passive smartphone sensing, and a wearable Fitbit device [Google]) during chemotherapy.
We enrolled 162 patients receiving outpatient chemotherapy into a 90-day prospective study. Patients were asked to install apps on their smartphones to rate daily symptoms and to collect passive sensor data and to wear a Fitbit device for the duration of the study. Participants completed baseline demographic and quality of life questionnaires, and clinical information was extracted from the electronic medical record. We fit a series of logistic generalized estimating equations to evaluate the association between demographic and clinical factors and daily engagement with each data stream.
Participants completed daily surveys on 61% (SD 27%) of days and collected sufficient smartphone data and wearable sensor data on 73% (SD 35%) and 70% (SD 33%) of enrolled days, respectively, on average. Relative to White participants, non-White patients demonstrated lower odds of engagement with both symptom surveys (odds ratio [OR] 0.49, 95% CI 0.29-0.81; P=.006) and wearable data collection (OR 0.35, 95% CI 0.17-0.73; P=.005). Patients with stage 4 cancer also exhibited lower odds of engagement with symptom reporting than those with earlier stage disease (OR 0.69, 95% CI 0.48-1.00; P=.048), and patients were less likely to complete symptom ratings on the weekend (OR 0.90, 95% CI 0.83-0.97; P=.008). Older patients (OR 1.03, 95% CI 1.01-1.06; P=.01) and those who reported better cognitive functioning at study entry (OR 1.18, 95% CI 1.03-1.34; P=.02) were more likely to engage with Fitbit data collection, and patients who reported higher levels of depressive symptoms were less likely to engage with smartphone data collection (OR 1.18, 95% CI 1.03-1.36; P=.02).
Remote patient monitoring during chemotherapy has the potential to improve clinical management, but only if patients engage with these systems. Our results suggest significant associations between demographic and clinical factors and long-term engagement with smartphone and wearable device assessments during chemotherapy. Non-White participants, those with metastatic cancer, or those with existing cognitive impairment may benefit from additional resources to optimize engagement. Contrary to hypotheses, older adults were more likely than younger adults to engage consistently with wearable device assessments.
化疗可引发一些症状,这些症状会损害生活质量和身体机能。在门诊治疗期间对日常症状和活动进行远程监测,或许能够更早地发现并处理新出现的毒性反应,但这要求患者,包括老年患者和急重症患者,使用技术手段通过智能手机报告症状,并为移动设备充电及佩戴。
本研究旨在确定与化疗期间参与者参与收集3种数据流(即每日患者报告症状调查、智能手机被动感应以及可穿戴式Fitbit设备[谷歌公司产品])相关的因素。
我们招募了162名接受门诊化疗的患者参与一项为期90天的前瞻性研究。要求患者在其智能手机上安装应用程序,以对每日症状进行评分、收集被动传感器数据,并在研究期间佩戴Fitbit设备。参与者完成了基线人口统计学和生活质量调查问卷,并从电子病历中提取了临床信息。我们拟合了一系列逻辑广义估计方程,以评估人口统计学和临床因素与各数据流每日参与度之间的关联。
参与者平均在61%(标准差27%)的天数完成了每日调查,分别在73%(标准差35%)和70%(标准差33%)的入组天数收集了足够的智能手机数据和可穿戴传感器数据。与白人参与者相比,非白人患者参与症状调查(比值比[OR]0.49,95%置信区间0.29 - 0.81;P = 0.006)和可穿戴数据收集(OR 0.35,95%置信区间0.17 - 0.73;P = 0.005)的可能性较低。与疾病分期较早的患者相比,4期癌症患者参与症状报告的可能性也较低(OR 0.69,95%置信区间0.48 - 1.00;P = 0.048),且患者在周末完成症状评分的可能性较小(OR 0.90,95%置信区间0.83 - 0.97;P = 0.008)。老年患者(OR 1.03,95%置信区间1.01 - 1.06;P = 0.01)以及在研究开始时报告认知功能较好的患者(OR 1.18,95%置信区间1.03 - 1.34;P = 0.02)更有可能参与Fitbit数据收集,而报告抑郁症状水平较高的患者参与智能手机数据收集的可能性较小(OR 1.18,95%置信区间1.03 - 1.36;P = 0.02)。
化疗期间的远程患者监测有改善临床管理的潜力,但前提是患者要参与这些系统。我们的结果表明,人口统计学和临床因素与化疗期间对智能手机和可穿戴设备评估的长期参与之间存在显著关联。非白人参与者、转移性癌症患者或存在认知障碍的患者可能需要额外资源来优化参与度。与假设相反,老年人比年轻人更有可能持续参与可穿戴设备评估。