This resource summarises public attitudes toward the use of patient data, based on research studies from 2010 to the present. It highlights key themes, such as support for using anonymised data for health research if there is public benefit, and concerns about industry using the data.

The Centre for Community Child Health has developed a toolkit to support the involvement of children and young people in research and service design.

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.