Clinical Governance Unit, Sydney Children's Hospitals Network, Randwick, New South Wales, Australia
Population Child Health, School of Women's and Children's Health, Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia.
BMJ Open. 2021 Dec 6;11(12):e050973. doi: 10.1136/bmjopen-2021-050973.
Children and young people with intellectual disability represent one of the most vulnerable groups in healthcare, yet they remain under-represented in projects to design, develop and/or improve healthcare service delivery. Increasingly, healthcare services are using various codesign and coproduction methodologies to engage children and young people in service delivery improvements.
This study employs an inclusive approach to the study design and execution, including two co-researchers who are young people with intellectual disability on the project team. We will follow an adapted experience-based co-design methodology to enable children and young people with intellectual disability to participate fully in the co-design of a prototype tool for eliciting patient experience data from children and young people with intellectual disability in hospital.
This study was granted ethical approval on 1 February 2021 by the Sydney Children's Hospitals Network Human Research Ethics Committee, reference number 2020/ETH02898. Dissemination plan includes publications, doctoral thesis chapter, educational videos. A summary of findings will be shared with all participants and presented at the organisation quality and safety committee.
儿童和青年智障人士是医疗保健中最脆弱的群体之一,但在设计、开发和/或改进医疗服务提供的项目中,他们的代表性仍然不足。越来越多的医疗服务正在使用各种共同设计和共同生产方法来让儿童和青年参与服务提供的改进。
本研究采用包容性的研究设计和执行方法,包括项目团队中的两名共同研究人员,他们是智障青年。我们将采用经过改编的基于经验的共同设计方法,使智障儿童和青年能够充分参与共同设计一种原型工具,以从医院中的智障儿童和青年中收集患者体验数据。
本研究于 2021 年 2 月 1 日获得了悉尼儿童医院网络人类研究伦理委员会的伦理批准,参考号为 2020/ETH02898。传播计划包括出版物、博士论文章节、教育视频。研究结果摘要将与所有参与者分享,并在组织质量和安全委员会上展示。