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 Centre for Population Health and Wellbeing Research provides a best practice guide to support researchers with co-production, along with three workshop reports that build on this guidance. These reports share work with young people to highlight research topics of importance.

Understanding Patient Data has compiled a summary of research and resources exploring public attitudes towards health data. Topics include trust in different organisations, opinions on decision-making, opt-out and choice, and how views differ among different groups of people.