Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthcare implementation

Author:

Murtagh Madeleine J.ORCID,Machirori Mavis,Gaff Clara L.,Blell Mwenza T.,de Vries JantinaORCID,Doerr Megan,Dove Edward S.ORCID,Duncanson Audrey,Hastings Ward Jillian,Hendricks-Sturrup Rachele,Ho Calvin W. L.ORCID,Johns Amber,Joly YannORCID,Kato KazutoORCID,Katsui Keiko,Kumuthini Judit,Maleady-Crowe Fiona,Middleton AnnaORCID,Milne RichardORCID,Minion Joel T.ORCID,Matshaba MogomotsiORCID,Mulrine Stephanie,Patch ChristineORCID,Ryan Rosalyn,Viney WilliamORCID

Abstract

Genomic science is increasingly central to the provision of health care. Producing and applying robust genomics knowledge is a complex endeavour in which no single individual, profession, discipline or community holds all the answers.  Engagement and involvement of diverse stakeholders can support alignment of societal and scientific interests, understandings and perspectives and promises better science and fairer outcomes. In this context we argue for F.A.I.R.E.R. data and data use that is Findable, Accessible, Interoperable, Reproducible, Equitable and Responsible. Yet there is a paucity of international guidance on how to engage publics, patients and participants in genomics. To support meaningful and effective engagement and involvement we developed an Engagement Framework for involving and engaging participants, patients and publics in genomics research and health implementation. The Engagement Framework is intended to support all those working in genomics research, medicine, and healthcare to deliberatively consider approaches to participant, patient and public engagement and involvement in their work. Through a series of questions, the Engagement Framework prompts new ways of thinking about the aims and purposes of engagement, and support reflection on the strengths, limitations, likely outcomes and impacts of choosing different approaches to engagement. To guide genomics activities, we describe four themes and associated questions for deliberative reflection: (i) fairness; (ii) context; (iii) heterogeneity, and (iv) recognising tensions and conflict. The four key components in the Engagement provide a framework to assist those involved in genomics to reflect on decisions they make for their initiatives, including the strategies selected, the participant, patient and public stakeholders engaged, and the anticipated goals. The Engagement Framework is one step in an actively evolving process of building genomics research and implementation cultures which foster responsible leadership and are attentive to objectives which increase equality, diversity and inclusion in participation and outcomes.

Funder

Medical Research Council

Economic and Social Research Council

H2020 European Research Council

Wellcome Trust

Publisher

F1000 Research Ltd

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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