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共同创建数字移动性结果的可视化:与患者的德尔菲式流程。

Cocreating the Visualization of Digital Mobility Outcomes: Delphi-Type Process With Patients.

作者信息

Lumsdon Jack, Wilson Cameron, Alcock Lisa, Becker Clemens, Benvenuti Francesco, Bonci Tecla, van den Brande Koen, Brittain Gavin, Brown Philip, Buckley Ellen, Caruso Marco, Caulfield Brian, Cereatti Andrea, Delgado-Ortiz Laura, Del Din Silvia, Evers Jordi, Garcia-Aymerich Judith, Gaßner Heiko, Gur Arieh Tova, Hansen Clint, Hausdorff Jeffrey M, Hiden Hugo, Hume Emily, Kirk Cameron, Maetzler Walter, Megaritis Dimitrios, Rochester Lynn, Scott Kirsty, Sharrack Basil, Sutton Norman, Vereijken Beatrix, Vogiatzis Ioannis, Yarnall Alison, Keogh Alison, Cantu Alma

机构信息

Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, United Kingdom.

School of Clinical Medicine, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.

出版信息

JMIR Form Res. 2025 May 9;9:e68782. doi: 10.2196/68782.

Abstract

BACKGROUND

Recent technological advances in wearable devices offer new potential for measuring mobility in real-world contexts. Mobilise-D has validated digital mobility outcomes to provide novel outcomes and end points in clinical research of 4 different long-term health conditions (Parkinson disease, multiple sclerosis, chronic obstructive pulmonary disease, and proximal femoral fracture). These outcomes also provide unique information that is important to patients; however, there is limited literature that explores the optimal methods to achieve this, such as the best way to visualize patients' data.

OBJECTIVE

This study aimed to identify meaningful outcomes for each condition and how to best visualize them from the perspective of end users.

METHODS

Using a Delphi-type protocol with patients as subject matter experts, we gathered iterative feedback on the cocreation of visualizations through 3 rounds of questionnaires. An open-ended questionnaire was used in round 1 to understand what aspects of mobility were most influenced by their health condition. These responses were mapped onto relevant digital mobility outcomes and walking experiences and then prioritized for visualization. Using patient responses, we worked alongside researchers, clinicians, and a patient advisory group to develop visualizations that depicted a week of mobility data. During rounds 2 and 3, participants rated usefulness and ease of understanding on a 5-point Likert scale and provided unstructured feedback in comment boxes for each visualization. Visualizations were refined using the feedback from round 2 before receiving further feedback in round 3.

RESULTS

Participation varied across rounds 1 to 3 (n=48, n=79, and n=78, respectively). Round 1 identified important outcomes and contexts for each health condition, such as walking speed and stride length for people with Parkinson disease or multiple sclerosis and number of steps for people with chronic obstructive pulmonary disease or proximal femoral fracture. The consensus was not reached for any visualization reviewed in round 2 or 3. Feedback was generally positive, and some participants reported that they were able to understand the visualization and interpret what the visualization represented.

CONCLUSIONS

Through the feedback provided and existing data visualization principles, we developed recommendations for future visualizations of mobility- and health-related data. Visualizations should be readable by ensuring that large and clear fonts are used and should be friendly for people with vision impairments, such as color blindness. Patients have a strong understanding of their own condition and its variability; hence, adding additional factors into visualizations is recommended to better reflect the nuances of a condition. Ensuring that outcomes and visualizations are meaningful requires close collaboration with patients throughout the development process.

摘要

背景

可穿戴设备的最新技术进展为在现实环境中测量活动能力提供了新的可能性。Mobilise-D已验证数字活动结果,以在4种不同的长期健康状况(帕金森病、多发性硬化症、慢性阻塞性肺疾病和股骨近端骨折)的临床研究中提供新的结果和终点。这些结果还提供了对患者很重要的独特信息;然而,探索实现这一目标的最佳方法(如可视化患者数据的最佳方式)的文献有限。

目的

本研究旨在从最终用户的角度确定每种状况的有意义的结果以及如何最好地对其进行可视化。

方法

采用以患者为主题专家的德尔菲式协议,我们通过三轮问卷调查收集了关于可视化共同创建的迭代反馈。第一轮使用开放式问卷来了解活动能力的哪些方面受其健康状况影响最大。这些回答被映射到相关的数字活动结果和步行体验上,然后确定优先进行可视化的内容。利用患者的回答,我们与研究人员、临床医生和一个患者咨询小组合作,开发出描绘一周活动数据的可视化。在第二轮和第三轮中,参与者用5点李克特量表对有用性和易理解性进行评分,并在每个可视化的评论框中提供非结构化反馈。在第二轮收到反馈后,根据反馈对可视化进行完善,然后在第三轮中接受进一步反馈。

结果

第一轮至第三轮的参与情况各不相同(分别为n = 48、n = 79和n = 78)。第一轮确定了每种健康状况的重要结果和背景,如帕金森病或多发性硬化症患者的步行速度和步幅,以及慢性阻塞性肺疾病或股骨近端骨折患者的步数。在第二轮或第三轮审查的任何可视化中都未达成共识。反馈总体上是积极的,一些参与者报告说他们能够理解可视化并解释其代表的内容。

结论

通过提供的反馈和现有的数据可视化原则,我们为未来与活动能力和健康相关的数据可视化制定了建议。可视化应确保使用大而清晰的字体以便于阅读,并且应对视力障碍者友好,如色盲患者。患者对自己的病情及其变异性有深刻的理解;因此,建议在可视化中加入其他因素以更好地反映病情的细微差别。确保结果和可视化有意义需要在整个开发过程中与患者密切合作。

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