This resource provides guidance on how to use accessible and simple language when talking about data to enhance communication with patients and the public.

National Co-ordinating Centre for Public Engagement (NCCPE) provides guidance and further resource on how to use evaluation to develop effective public engagement practice and to inform culture change.

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.