Kolovson Samantha, Pratap Abhishek, Duffy Jaden, Allred Ryan, Munson Sean A, Areán Patricia A
Human Centered Design & Engineering, University of Washington.
Biomedical Informatics & Medical Education, University of Washington Sage Bionetworks.
Int Conf Pervasive Comput Technol Healthc. 2020 May;2020:347-362. doi: 10.1145/3421937.3422025.
Digital psychiatry is a rapidly growing area of research. Mobile assessment, including passive sensing, could improve research into human behavior and may afford opportunities for rapid treatment delivery. However, retention is poor in remote studies of depressed populations in which frequent assessment and passive monitoring are required. To improve engagement and understanding participant needs overall, we conducted semi-structured interviews with 20 people representative of a depressed population in a major metropolitan area. These interviews elicited feedback on strategies for long-term remote research engagement and attitudes towards passive data collection. Our results found participants were uncomfortable sharing vocal samples, need researchers to take a more active role in supporting their understanding of passive data collection, and wanted more transparency on how data were to be used in research. Despite these findings, participants trusted researchers with the collection of passive data. They further indicated that long term study retention could be improved with feedback and return of information based on the collected data. We suggest that researchers consider a more educational consent process, giving participants a choice about the types of data they share in the design of digital health apps, and consider supporting feedback in the design to improve engagement.
数字精神病学是一个快速发展的研究领域。包括被动传感在内的移动评估可以改善对人类行为的研究,并可能为快速提供治疗创造机会。然而,在对抑郁症患者进行的远程研究中,留存率很低,因为这类研究需要频繁评估和被动监测。为了提高参与度并全面了解参与者的需求,我们对大城市地区20名具有代表性的抑郁症患者进行了半结构化访谈。这些访谈收集了关于长期远程研究参与策略以及对被动数据收集态度的反馈。我们的结果发现,参与者对分享语音样本感到不舒服,需要研究人员在帮助他们理解被动数据收集方面发挥更积极的作用,并且希望在研究中使用数据的方式上有更多透明度。尽管有这些发现,参与者信任研究人员收集被动数据。他们进一步表示,通过基于收集到的数据提供反馈和信息返还,可以提高长期研究的留存率。我们建议研究人员考虑采用更具教育性的知情同意程序,让参与者在数字健康应用程序设计中选择他们分享的数据类型,并考虑在设计中支持反馈以提高参与度。