CPROR is working with international collaborators to develop best practice for PROs in clinical trials. This includes the selection of PROs, trial design (including the development of a SPIRIT-PRO extension), minimising missing data, managing PRO Alerts and the transparent reporting of PRO data (using CONSORT-PRO) to maximise impact and patient benefit.
EPiC: Evaluation of Patient-Reported Outcome (PRO) Protocol Content and Reporting in UK Cancer Clinical Trials
SPIRIT-PRO Standard Protocol Items: Recommendations for Interventional Trials Patient-Reported Outcome Extension
PRO-IMPACT Impact of PRO trial data on health policy and clinical practice
PARTNERS: Collaborative care for people with serious mental illness (Core Outcome Set Development)
Techniques to include carers' quality of life in economic evaluation
Assessing Impact and Directing treatment in patients with Uveitic Macular Oedema (AID UMO) Study
IMPRESS-AF: IMproved exercise tolerance in heart failure with PReserved Ejection fraction by Spironolactone on myocardial fibrosiS in Atrial Fibrillation.