收集被动智能手机数据用于家庭护理人员和晚期癌症患者数字表型分析的可行性和可接受性。

IF 3.3 Q2 ONCOLOGY
JCO Clinical Cancer Informatics Pub Date : 2025-01-01 Epub Date: 2025-01-02 DOI:10.1200/CCI-24-00201
J Nicholas Odom, Kyungmi Lee, Erin R Currie, Kristen Allen-Watts, Erin R Harrell, Avery C Bechthold, Sally Engler, Kayleigh Curry, Arif H Kamal, Christine S Ritchie, George Demiris, Alexi A Wright, Marie A Bakitas, Andres Azuero
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引用次数: 0

摘要

目的:对被动收集的智能手机传感器数据(称为数字表型)进行建模,有可能发现家庭照顾者和晚期癌症患者的痛苦,并可能导致癌症护理的新型临床模型。本研究的目的是评估从患有晚期癌症的家庭照顾者及其照顾者收集24周以上被动智能手机数据的可行性和可接受性。方法:观察性可行性研究。通过诊所或社交媒体招募家庭护理人员和晚期癌症患者,并将数字表型应用程序(Beiwe)下载到他们的智能手机中,该应用程序在24周内被动收集传感器数据。通过量化入学人数和保留率以及获得的数据量来评估可行性。通过24周后的定性访谈评估可接受性。结果:在接触的178对护理人员和患者中,22.5%的护理人员(n = 40)和10.1%的患者(n = 18)都同意这项研究并成功下载了应用程序,其中大多数是通过社交媒体招募的(93%)。在24周(168天)中,收到数据的中位数天数为141天。访谈产生了三个主题:(1)尽管存在一些技术挑战,但研究过程的经验总体上是积极的;(2)安全和隐私问题最小,通过清晰的解释、对医疗保健系统的信任和隐私规范来缓解;(3)使用被动智能手机监测自动触发援助的临床模型可能是有益的,但要注意虚报。结论:这项收集被动智能手机数据的试点研究发现,可行性指标好坏参半,注册率不理想,特别是通过诊所,但注册者的留存率和数据收集率是积极的。参与者普遍对被动监控持积极态度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Feasibility and Acceptability of Collecting Passive Smartphone Data for Potential Use in Digital Phenotyping Among Family Caregivers and Patients With Advanced Cancer.

Purpose: Modeling passively collected smartphone sensor data (called digital phenotyping) has the potential to detect distress among family caregivers and patients with advanced cancer and could lead to novel clinical models of cancer care. The purpose of this study was to assess the feasibility and acceptability of collecting passive smartphone data from family caregivers and their care recipients with advanced cancer over 24 weeks.

Methods: This was an observational feasibility study. Family caregivers and patients with advanced cancer were recruited through clinic or via social media and downloaded a digital phenotyping application (Beiwe) to their smartphones that passively collected sensor data over 24 weeks. Feasibility was evaluated by quantifying enrollment and retention and the quantity of acquired data. Acceptability was assessed through post-24 week qualitative interviews.

Results: Of 178 caregiver and patient dyads approached, 22.5% of caregivers (n = 40) and 10.1% of patients (n = 18) both consented to the study and successfully downloaded the application, with most recruited through social media (93%). Of 24 weeks (168 days), the median number of days that data were received was 141 days. Interviews yielded three themes: (1) experiences with study procedures were generally positive despite some technical challenges; (2) security and privacy concerns were minimal, mitigated by clear explanations, trust in the health care system, and privacy norms; and (3) a clinical model that used passive smartphone monitoring to automatically trigger assistance could be beneficial but with concern about false alarms.

Conclusion: This pilot study of collecting passive smartphone data found mixed indicators of feasibility, with suboptimal enrollment rates, particularly via clinic, but positive retention and data collection rates for those who did enroll. Participants had generally positive views of passive monitoring.

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来源期刊
CiteScore
6.20
自引率
4.80%
发文量
190
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