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成骨不全症青少年电子健康项目的设计、开发与可用性测试:一项两阶段以用户为中心的混合方法研究方案

The Design, Development, and Usability Testing of an eHealth Program for Youths With Osteogenesis Imperfecta: Protocol for a 2-Phase User-Centered Mixed Methods Study.

作者信息

Tsimicalis Argerie, Stinson Jennifer, Thorstad Kelly, Rauch Frank, Hamdy Reggie, Chougui Khadidja, Addab Sofia, Palomo Telma, Bernstein Mitchell, Dahan-Oliel Noemi, Veilleux Louis-Nicolas, Massochin Nunes Pinto Laura, Passos Dos Santos Raissa

机构信息

Shriners Hospitals for Children-Canada, Montreal, QC, Canada.

The Hospital for Sick Children, Toronto, ON, Canada.

出版信息

JMIR Res Protoc. 2023 Jun 23;12:e47524. doi: 10.2196/47524.

Abstract

BACKGROUND

Innovative approaches are needed to address the self-management needs of youths with osteogenesis imperfecta (OI) transitioning into adult-oriented health care systems. Using a sequentially phased research approach, the goal is to design, develop, and test the usability of an innovative eHealth program called "Teens Taking Charge: Managing OI Online," hereafter named "Teens OI." This program seeks to optimize self-management, facilitate a successful transition to adult care, and address a critical gap in the quality of care for youths with OI.

OBJECTIVE

The study objectives are to (1) design and develop an English and French version of the Teens OI and (2) test the usability of the Teens OI in terms of efficiency, effectiveness, and satisfaction from the perspectives of youths with OI and their parents.

METHODS

A user-centered design is presently in progress to design and develop Teens OI. A "Website Design and Development Council" (ie, Council) has been convened, with 20 youths and parent dyads recruited and global experts surveyed at an international meeting. With unanimous support from the Council, usability testing of the Teens OI will ensue in 4 iterative cycles with 32 youth-parent dyads. All sociodemographic and usability metrics will be descriptively analyzed. All recorded interview and focus group data are analyzed using content analysis techniques involving an iterative process of data reduction, data display, conclusion drawing, and verification.

RESULTS

As of December 2022, an 8-person, interdisciplinary Teens OI council, comprising 4 health care professionals, 3 youths and young adults with OI, and 1 parent, has been convened to oversee the design and development of Teens OI. Two cycles of interviews have been conducted with 10 youths with OI with or without their parents (n=6) from December 2021 to September 2022. Data analysis has been in progress since April 2022. Aim 2 is ethically approved and will commence following the completion of content development, expected by late July 2023. Preliminary analysis indicates that the following topics need to be prioritized for the youths: mental health, pain, accessibility, medical care, education, community, and parental care.

CONCLUSIONS

The proposed study will design and develop a self-management and transitional care program for youths with OI in partnership with patients, caregivers, and health care professionals. This study leverages youths' openness to adopt eHealth technologies to meet their needs and has the potential to actively engage them to autonomously manage their lifelong conditions, and facilitate a successful transition to adult health care. Finally, the proposed study will also address a critical gap in the quality of care and the growing concern that the OI population transitioning from pediatric to adult care is at risk of various adverse events associated with the transition.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/47524.

摘要

背景

需要创新方法来满足成骨不全症(OI)青少年向成人医疗保健系统过渡时的自我管理需求。采用分阶段的研究方法,目标是设计、开发并测试一个名为“青少年自主管理:在线管理OI”(以下简称“青少年OI”)的创新型电子健康项目的可用性。该项目旨在优化自我管理,促进向成人护理的顺利过渡,并解决OI青少年护理质量方面的关键差距。

目的

研究目标是(1)设计并开发青少年OI的英文和法文版本,以及(2)从OI青少年及其父母的角度,测试青少年OI在效率、有效性和满意度方面的可用性。

方法

目前正在进行以用户为中心的设计,以设计和开发青少年OI。已召集了一个“网站设计与开发委员会”(即委员会),招募了20对青少年和父母,并在一次国际会议上对全球专家进行了调查。在委员会的一致支持下,将对青少年OI进行4个迭代周期的可用性测试,涉及32对青少年-父母。将对所有社会人口统计学和可用性指标进行描述性分析。所有记录的访谈和焦点小组数据都使用内容分析技术进行分析,该技术涉及数据简化、数据展示、得出结论和验证的迭代过程。

结果

截至2022年12月,已召集了一个由8人组成的跨学科青少年OI委员会,其中包括4名医疗保健专业人员、3名患有OI的青少年和青年以及1名家长,以监督青少年OI的设计和开发。从2021年12月到2022年9月,已对10名患有或未患有OI的青少年(n = 6)及其父母进行了两轮访谈。自2022年4月以来一直在进行数据分析。目标2已获得伦理批准,并将在内容开发完成后开始,预计在2023年7月下旬完成。初步分析表明,对于青少年来说,以下主题需要优先考虑:心理健康、疼痛、可及性、医疗护理、教育、社区和父母照顾。

结论

拟议的研究将与患者、护理人员和医疗保健专业人员合作,为OI青少年设计并开发一个自我管理和过渡性护理项目。本研究利用青少年对采用电子健康技术的开放态度来满足他们的需求,并有可能积极促使他们自主管理自己的终身疾病,促进向成人医疗保健的顺利过渡。最后,拟议的研究还将解决护理质量方面的关键差距,以及越来越多的担忧,即从儿科护理过渡到成人护理的OI患者群体面临与过渡相关的各种不良事件的风险。

国际注册报告识别号(IRRID):DERR1-10.2196/47524。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/122a/10337436/3e1df2ec2063/resprot_v12i1e47524_fig1.jpg

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