Protocol for an umbrella review of the state-of-science on public and patient involvement in health and social care research with children, young people and families.

HRB open research Pub Date : 2025-07-14 eCollection Date: 2025-01-01 DOI:10.12688/hrbopenres.14142.1
Shauna Malone Gill, Orla Hayes, Yvonne Corcoran, Anna Gunning, Veronica Swallow, Emma Nicholson, Begonya Nafria Escalera, Amanda Drury, Edel Murphy, Arthur Templeman-Lilley, Veronica Lambert
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引用次数: 0

Abstract

Background: Public and Patient Involvement (PPI) refers to the active collaboration of patients and the public in health and social care research decision-making, enhancing research success, cost-effectiveness, and impact. Children, young people, and their families bring unique lived experiences to PPI in research, relating to others with similar experiences, while factors like age, cognitive maturation, and developmental stage create differences between researchers and patients or the public. Collaboration with children, young people, and their families should be guided by specific project context and a strong evidence base. However, existing systematic reviews reveal inconsistencies in reporting and a lack of standardised methods for these groups, limiting effective PPI implementation. This protocol details methods for an umbrella review to identify the current state-of-science and future priorities for collaborating with children, young people and families in health and social care research.

Methods: The protocol was developed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P) guidelines, which will also direct the reporting of findings. The Joanna Briggs Institute's methodology for conducting umbrella reviews will be adhered to throughout. MEDLINE, CINAHL, EMBASE, PsycINFO, Cochrane, DARE, JBI Evidence Synthesis, PROSPERO, grey literature databases, targeted international networks, and the Google search engine will be searched for systematic reviews on PPI with children, young people, and families in health and social care research. Two reviewers will independently conduct eligibility screening, data extraction, and quality appraisal.

Conclusions: This umbrella review will provide critical insights into the state-of-science of PPI with children, young people and families in health and social care research. The synthesis of findings could yield important information for researchers and other stakeholders conducting health and social care research in collaboration with children, young people and families by highlighting key patterns, gaps, and recommendations to guide future PPI practices, policies, and research.

Registration: This umbrella review was registered in PROSPERO, the International Prospective Register of Systematic Reviews (Prospero registration number: CRD42024608935, registered 14th of November 2024).

对公众和病人参与儿童、青年和家庭保健和社会护理研究的科学现状进行总括审查的议定书。
背景:公众和患者参与(PPI)是指患者和公众在卫生和社会保健研究决策中的积极合作,以提高研究的成功率、成本效益和影响。儿童、年轻人及其家庭为PPI研究带来了独特的生活经历,与其他有类似经历的人有关,而年龄、认知成熟度和发育阶段等因素则造成了研究人员与患者或公众之间的差异。与儿童、青年及其家庭的合作应以具体的项目背景和强有力的证据基础为指导。然而,现有的系统评价显示,这些群体的报告不一致,缺乏标准化的方法,限制了PPI的有效实施。本议定书详细说明了总括性审查的方法,以确定在卫生和社会保健研究中与儿童、青年和家庭合作的当前科学状况和未来优先事项。方法:该方案是根据系统评价和荟萃分析方案的首选报告项目(PRISMA-P)指南制定的,该指南也将指导研究结果的报告。乔安娜·布里格斯研究所进行总括性审查的方法将始终得到遵守。MEDLINE、CINAHL、EMBASE、PsycINFO、Cochrane、DARE、JBI Evidence Synthesis、PROSPERO、灰色文献数据库、有针对性的国际网络和谷歌搜索引擎将检索健康和社会保健研究中儿童、青少年和家庭PPI的系统综述。两名审稿人将独立进行资格筛选、数据提取和质量评估。结论:这项总括性的综述将为儿童、青少年和家庭在健康和社会保健研究中的PPI的科学现状提供重要的见解。研究结果的综合可以通过突出关键模式、差距和指导未来PPI实践、政策和研究的建议,为与儿童、年轻人和家庭合作开展卫生和社会保健研究的研究人员和其他利益攸关方提供重要信息。注册:本总结性综述已在普洛斯彼罗注册(普洛斯彼罗注册号:CRD42024608935,于2024年11月14日注册)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.40
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