Suppr超能文献

开发一种数字工具包以改善系统性红斑狼疮患者的生活质量。

Development of a digital toolkit to improve quality of life of patients with systemic lupus erythematosus.

作者信息

Leung Jerik, Kloos Laura, Kim Alfred Hj, Baker Elizabeth A

机构信息

Department of Behavioral Science and Health Education, College for Public Health and Social Justice, Saint Louis University, USA.

Transtria LLC, USA.

出版信息

Digit Health. 2021 Aug 10;7:20552076211033423. doi: 10.1177/20552076211033423. eCollection 2021 Jan-Dec.

Abstract

OBJECTIVE

The purpose of this manuscript is to detail development and initial usability testing of an e-toolkit designed to provide skills and knowledge around self-management behaviors for individuals living with systemic lupus erythematosus.

METHODS

Researchers worked with a steering committee of patients and providers to (1) develop a clickable prototype of an e-toolkit and (2) conduct alpha (individuals not affiliated with an academic clinic as patient or provider) and beta (individual patients with systemic lupus erythematosus as well as members of the clinic healthcare team and individuals who work in patient advocacy organizations) usability testing through semistructured interviews.

RESULTS

During the review of the e-toolkit, the feedback provided by participants in both alpha and beta groups centered on two overarching themes: (1) improving user interface and materials and (2) integration of information and supports between toolkit and clinical personnel.

CONCLUSION

Digital approaches that are tailored to individual symptom variation and integrated with a clinical system have the opportunity to enhance ongoing clinical care. These findings support movement toward integrated, team-based care models, tailored digital resources, and use of expanded virtual interaction options to ensure on-going engagement between healthcare providers and systemic lupus erythematosus patients.

摘要

目的

本手稿旨在详细介绍一个电子工具包的开发及初步可用性测试情况,该工具包旨在为系统性红斑狼疮患者提供有关自我管理行为的技能和知识。

方法

研究人员与患者和医疗服务提供者组成的指导委员会合作,(1)开发一个可点击的电子工具包原型,(2)通过半结构化访谈进行阿尔法测试(参与者为非学术诊所的患者或医疗服务提供者)和贝塔测试(参与者为系统性红斑狼疮患者个体、诊所医疗团队成员以及在患者权益倡导组织工作的人员)。

结果

在对电子工具包的审查过程中,阿尔法组和贝塔组参与者提供的反馈集中在两个总体主题上:(1)改进用户界面和材料,(2)工具包与临床人员之间的信息整合与支持。

结论

针对个体症状差异量身定制并与临床系统相结合的数字方法,有机会加强持续的临床护理。这些发现支持朝着综合的、基于团队的护理模式、量身定制的数字资源以及使用扩展的虚拟互动选项发展,以确保医疗服务提供者与系统性红斑狼疮患者之间的持续互动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f101/8365175/5c855105f971/10.1177_20552076211033423-fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验