Defining patient preferences and priorities for treatment options and outcomes in epilepsy

Project Summary: This study aims: (i) to identify which healthcare interventions are considered important by people with epilepsy and how different patient subgroups prioritise different interventions; (ii) to identify which outcomes of healthcare interventions are considered important by people with epilepsy, and how the different patient subgroups prioritise different outcomes; (iii) to identify views and definitions of equivalence for outcomes used in clinical trials among people with epilepsy, and to investigate perceptions of acceptable trade-offs between benefits and harm across the different subgroups.