Katrine Westergaard, Ritzel Signe Baattrup, Caroline Krogh, Marie Lynning, Olsgaard Bergien Sofie, Lasse Skovgaard
The Danish Multiple Sclerosis Society, Valby, Denmark.
Digit Health. 2021 Nov 26;7:20552076211055552. doi: 10.1177/20552076211055552. eCollection 2021 Jan-Dec.
Digital tools offer new ways of collecting outcome data in intervention research. Little is known about the potentials and barriers of using such tools for outcome measurement in multiple sclerosis trials. This study aimed to examine reporting adherence and barriers experienced by people with multiple sclerosis in an intervention study using three different digital tools for outcome measurement.
This was a mixed-methods study conducted in the context of a randomized controlled trial. Data collected during the randomized controlled trial were analysed to assess reporting adherence. Twenty-three semi-structured, in-depth interviews were conducted to investigate randomized controlled trial participants' experiences.
Reporting adherence was high for all three measurement tools, but lower in the control group. Four main barriers were defined: (1) the self-monitoring aspect and repeated tests imbedded in the digital tools affected participants' behavior during the randomized controlled trial. (2) Self-monitoring caused some participants to worry more about their health. (3) Passively collected data did not always correspond with participants' own experiences, which caused them to question the validity of the collected data. (4) Daily reporting using different digital tools placed a significant burden on participants.
The study indicates a high reporting adherence using digital tools among people with multiple sclerosis. However, future studies should carefully consider the overall burden imposed on participants when taking this approach. Measures should be taken to avoid the potential unintended effects of the self-monitoring and gamification aspects of using digital tools. These measures could include passive monitoring, reducing the frequency of reporting and blinding participants to their own data.
数字工具为干预研究中收集结果数据提供了新方法。对于在多发性硬化症试验中使用此类工具进行结果测量的潜力和障碍,人们了解甚少。本研究旨在调查在一项干预研究中,使用三种不同数字工具进行结果测量时,多发性硬化症患者的报告依从性及遇到的障碍。
这是一项在随机对照试验背景下进行的混合方法研究。对随机对照试验期间收集的数据进行分析,以评估报告依从性。进行了23次半结构化深入访谈,以调查随机对照试验参与者的体验。
所有三种测量工具的报告依从性都很高,但对照组的依从性较低。确定了四个主要障碍:(1)数字工具中嵌入的自我监测方面和重复测试影响了参与者在随机对照试验期间的行为。(2)自我监测使一些参与者更加担心自己的健康。(3)被动收集的数据并不总是与参与者自身的体验相符,这使他们对所收集数据的有效性产生质疑。(4)使用不同数字工具进行每日报告给参与者带来了沉重负担。
该研究表明,多发性硬化症患者使用数字工具时报告依从性较高。然而,未来的研究在采用这种方法时应仔细考虑给参与者带来的总体负担。应采取措施避免使用数字工具时自我监测和游戏化方面可能产生的意外影响。这些措施可包括被动监测、减少报告频率以及让参与者对自己的数据不知情。