Establishing a set of acceptable demographic questions for use in health research through public consultation

Abstract Background The importance of inclusivity in health care and health research is increasingly recognised in the UK. However, there are currently no UK standards for collecting self-reported demographic data from research participants. To address this gap, we undertook a public involvement act...

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Autors principals:	Emma Lidington, Morgaine Stiles, Jessica Maudsley, Jennifer Ching, Andy Deutsch, Natasha Lipman, Emily Williamson, Georgiana Synesi, Karen Poole, Eleanor Knuckey, Tahera Hussain, Christina Derksen, Hannah Drysdale, Laura White, Georgia Mannion-Krase, Cherrelle Salmon, Jane Rigney, Beth Stuart, Rebecca Lewis
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2026-01-01
Col·lecció:	Research Involvement and Engagement
Matèries:	Demographics Inclusivity Diversity Patient and public involvement Public consultation Trial participation
Accés en línia:	https://doi.org/10.1186/s40900-026-00836-1
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