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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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Equality, diversity and inclusion (EDI) toolkit for researchers

Newcastle University have created an EDI Toolkit for researchers, to support understanding about EDI issues in and around research. Resources include an accessibility guide, allyship guide, inclusive language guide and inclusive behaviours guide.
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Data Literacy Course

DATAMIND and The McPin Foundation created this course to help people understand how the NHS uses and stores health data, including patient rights, how researchers use data, and the risks and benefits. It’s especially useful for those who have used NHS mental health services.
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