This Health Data Research UK bite-sized video explores the importance of trust in clinical trials that use healthcare data. It explains some of the reasons why trust varies across populations and its implications for promoting inclusivity in trial participation.

The National Institute for Health and Care Research (NIHR) Policy Research Unit in Maternal and Neonatal Health and Care (PRU-MNHC) share key themes identified from their research project, to support researchers to engage and involve people who are currently under-represented in health research.

This resource provides information to help guide researchers on planning, delivering, and evaluating public involvement activities, with tips, templates, and insights on participation and engagement.