What is Patient and public involvement?
We are committed to actively involving patients and the public in our research.
Patient and public involvement (PPI) in research is research that is carried out ‘with’ or ‘by’ patients and/or members of the public rather than ‘to’, ‘about’ or ‘for’ them. At the MRC CTU this includes welcoming patients as members of trial steering groups and asking them for comments on patient information leaflets. It also includes consulting them about particular trial proposals. We have patients sitting on groups and committees where appropriate, for example our Trial Protocol Review Committee.
We use the term ‘patients and public’ to include current, former and potential patients, carers, people who use health and social care services, and people from organisations that represent people who use these services.