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<p>Rare diseases predominantly affect children and young people (CYP). Current research involving CYP often fails to adequately represent those from lower socioeconomic backgrounds, contributing to widening health and research inequalities. This concise report proposes a framework to build on successful methods that were able to engage with underrepresented CYP. This was achieved through partnership with social enterprise organisations and utilised connections in the community to provide positive knowledge exchange of local services that may enhance their socioeconomic situation, in turn for engaging on how to improve services or advance research. These insights, together with information from scoping the field, were used to develop a practical framework for inclusive Patient and Public Involvement and Engagement (PPIE) with CYP. This framework has been initially designed to be evaluated in CYP with rare kidney diseases, as an exemplar long term health condition. The model of ‘PPIE through collaborative empowerment’ leverages existing community trust to reduce barriers to participation, hopefully opening the door to more representative views from children residing in regions of low socioeconomic status. The framework has potential to be adapted to address other inequalities or adaptation for different diseases, hopefully offering a replicable approach to representative research design. The next stages of this research are to implement the framework and formally evaluate its success.</p>

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A framework to amplify the voices of underrepresented children and young people in rare disease research

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年3月31日

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  • L. Thomas,
  • J. Preston,
  • H. Hardwick,
  • J.D. Peipert,
  • L. Oni

摘要

Rare diseases predominantly affect children and young people (CYP). Current research involving CYP often fails to adequately represent those from lower socioeconomic backgrounds, contributing to widening health and research inequalities. This concise report proposes a framework to build on successful methods that were able to engage with underrepresented CYP. This was achieved through partnership with social enterprise organisations and utilised connections in the community to provide positive knowledge exchange of local services that may enhance their socioeconomic situation, in turn for engaging on how to improve services or advance research. These insights, together with information from scoping the field, were used to develop a practical framework for inclusive Patient and Public Involvement and Engagement (PPIE) with CYP. This framework has been initially designed to be evaluated in CYP with rare kidney diseases, as an exemplar long term health condition. The model of ‘PPIE through collaborative empowerment’ leverages existing community trust to reduce barriers to participation, hopefully opening the door to more representative views from children residing in regions of low socioeconomic status. The framework has potential to be adapted to address other inequalities or adaptation for different diseases, hopefully offering a replicable approach to representative research design. The next stages of this research are to implement the framework and formally evaluate its success.