开展患者和临床医生参与式设计会议,为成人哮喘患者开发以用户为中心的移动应用程序

Amanda Miao, Doreen Khakshour, Emine Cosar, Brian C. Hsia, Kai Zheng, Savneet Kaur, A. Singh, Obumneme Njeze, Jonathan Feldman, Marina Reznik, S. Jariwala
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摘要

目的:ASTHMAXcel是一个面向患者的移动健康自我管理应用程序,与改善哮喘知识和临床结果相关。本研究的目的是获得成人患者和初级保健临床医生对哮喘患者的ASTHMAXcel移动应用程序的反馈。材料和方法:我们进行了两次参与式设计会议;一个是服务不足的成年患者,另一个是门诊初级保健临床医生。评估了参与者对当前哮喘护理差距、哮喘应用程序的有用性和应用程序的期望功能的态度。使用专题地图对数据进行定性分析,并使用关联图进行结构化。结果:9名患者(67%,平均年龄48.0)和7名临床医生(71%,平均年龄54.6)参与了研究。两组的定性分析表明哮喘患者的教育、自我跟踪、同伴支持和激励内容都有所改善。所有参与者都承认,患者错过了哮喘恶化的迹象,缺乏适当的自我管理知识。患者和临床医生都建议增加具体的教育内容,包括药物副作用和呼吸练习。他们希望能够追踪整个医院系统的症状、药物和就诊情况。患者建议社会参与是减少与哮喘相关的污名化的一种方式。结论:参与式设计会议使受试者反馈能够指导哮喘maxcel的改进,并促进了哮喘maxcel PRO的开发,这是一个包含许多讨论功能的更新应用程序。主要的更新包括自我跟踪患者报告的结果(PROs),量身定制的药物提醒,以及鼓励收集PROs的用户排行榜。
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Conducting Patient and Clinician Participatory Design Sessions to Create a User-Centered Mobile Application for Adults with Asthma
Objective: ASTHMAXcel is a patient-facing mobile health self-management application associated with improvements in asthma knowledge and clinical outcomes. The goal of this study was to gain feedback from adult patients and primary care clinicians regarding the ASTHMAXcel mobile app for asthma patients. Materials and Methods: We conducted two participatory design sessions; one with underserved adult patients and one with outpatient primary care clinicians. Participant attitudes were assessed regarding current asthma care gaps, the usefulness of asthma apps, and desired features of an app. Thematic maps were used to qualitatively analyze the data and structured using affinity diagrams. Results: Nine patients (67% F, mean age 48.0) and seven clinicians (71% F, mean age 54.6) participated in the study. Qualitative analyses of both groups suggested the improvement in education of patients with asthma, self-tracking, peer support, and motivational content. All participants acknowledged that patients miss signs of asthma exacerbations and lack the knowledge for appropriate self-management. Both patients and clinicians recommended adding specific educational content including medication side effects and breathing exercises. They sought the ability to track symptoms, medications, and visits across hospital systems. Patients suggested social engagement as a way of reducing stigmatization related to asthma. Conclusion: Participatory design sessions enabled subject feedback to guide the refinement of ASTHMAXcel and facilitated the development of ASTHMAXcel PRO, an updated app encompassing many of the discussed features. Main updates include self-tracking patient-reported outcomes (PROs), tailored medication reminders, and a user leaderboard to encourage the collection of PROs.
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