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患者和公众参与开发数字工具 MyBoT,以支持慢性病青少年与护理提供者之间的沟通。

Patient and public involvement in the development of the digital tool MyBoT to support communication between young people with a chronic condition and care providers.

机构信息

Department Perspective of Patients and Clients in Healthcare, Nivel, The Netherlands Institute for Health Services Research, Utrecht, The Netherlands.

JongPIT, Amsterdam, The Netherlands.

出版信息

Health Expect. 2024 Apr;27(2):e14003. doi: 10.1111/hex.14003.

Abstract

INTRODUCTION

To guide good practices in patient and public involvement (PPI), several calls have been made to share detailed accounts of practical experiences. We describe our collaboration with young people with a chronic condition (YPCC) in the development, testing and implementation of the digital communication tool MyBoT (Map your Burden of Treatment).

METHODS

MyBoT was developed by a team of academic researchers, some of whom were practising care providers, YPCC and designers. In addition to the two co-researchers in the research team, various groups of YPCC were involved in decision-making through participation in a design session, workshops and a dialogue session. The Involvement Matrix was used to reflect on the PPI of all YPCC.

RESULTS

Initially, the two co-researchers were involved in the roles of informer and co-thinker, but their decision-making power within the study increased over time. In the final stages of the study, the co-researchers and researchers became partners. The other YPCC who participated in the different sessions and workshops were co-thinkers in all stages of the study.

CONCLUSION

The PPI of two YPCCs as co-researchers within the research team ensured continuous involvement, whereas the PPI of various groups of YPCCs guaranteed a representative and inclusive approach. Researchers play an essential role in bringing all perspectives together, integrating them within the technical and financial constraints and ultimately building a tool that is tailored to its users' needs.

PATIENT OR PUBLIC CONTRIBUTION

YPCC played a significant role in the present study. Two YPCC-who are also co-authors of this paper-were involved in all stages of this project as members of the research team. In addition, various YPCCs were involved in the development, testing and implementation stage of MyBoT by organizing design sessions, workshops and a dialogue session.

摘要

简介

为了指导患者和公众参与(PPI)的良好实践,已经多次呼吁分享实践经验的详细说明。我们描述了我们与患有慢性疾病的年轻人(YPCC)在开发、测试和实施数字通信工具 MyBoT(Map your Burden of Treatment)方面的合作。

方法

MyBoT 由一个学术研究团队开发,其中一些成员是执业护理提供者、YPCC 和设计师。除了研究团队中的两位共同研究员外,还通过参与设计会议、研讨会和对话会议,让不同群体的 YPCC 参与决策。利用参与矩阵来反思所有 YPCC 的 PPI。

结果

最初,两位共同研究员担任信息提供者和共同思考者的角色,但随着时间的推移,他们在研究中的决策权力增加。在研究的最后阶段,共同研究员和研究人员成为合作伙伴。在不同会议和研讨会上参与的其他 YPCC 是研究各个阶段的共同思考者。

结论

研究团队中两名 YPCC 作为共同研究员的 PPI 确保了持续参与,而不同群体的 YPCC 的 PPI 则保证了代表性和包容性方法。研究人员在将所有观点汇集在一起、在技术和财务限制范围内整合它们以及最终构建适合用户需求的工具方面发挥着至关重要的作用。

患者或公众的贡献

YPCC 在本研究中发挥了重要作用。两名 YPCC-也是本文的共同作者-作为研究团队的成员参与了该项目的所有阶段。此外,通过组织设计会议、研讨会和对话会议,各种 YPCC 参与了 MyBoT 的开发、测试和实施阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3c3/10915502/5d2743ddf6d9/HEX-27-e14003-g002.jpg

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