Participant characteristics and reasons for non-consent to health information linkage for research: experiences from the ATHENA COVID-19 study – Kim Greaves et al.
The linkage of primary care, hospital and other health registry data is a global goal, and a consent-based approach is often used. Understanding the attitudes of why participants take part is important, yet little is known about reasons for non-participation. The ATHENA COVID-19 feasibility study [...]