This guide helps public involvement and engagement professionals and researchers to collaborate with the public and patients, valuing their lived experiences to co-create easy to understand information. This ensures everyone equally grasps the benefit of health data.

Health Data Research UK commissioned this review to collate existing literature on public attitudes towards the collection and use of their health data across the UK.

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.