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Engaging underserved groups in routine data trials

This Health Data Research UK bite-sized video covers strategies to build trust and engage underserved communities in data-enabled clinical trials. You will discover how partnerships, co-design and addressing barriers to participation can foster inclusivity and improve diversity in trial participation.
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Data Saves Lives Toolkit: Having positive conversations about health data

A toolkit from Data Saves Lives to equip patient groups and health influencers with the information and materials they need to have a positive dialogue with their communities about health data.
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A guide to creating inclusive content and language

National Institute for Health Research (NIHR) provides guidance and best practice for inclusive writing.
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