Realist evaluation does offer a way forward towards improving the evidence base for PPI in research. Both the patients and the public can contribute significantly.
Patients and members of the public possess a wealth of knowledge, skills and experience and, therefore, can help push research forward at different levels. As an example, local community leaders can enhance recruitment; patients with the condition being researched upon can provide hints on layout/design of study protocol documents and thus improve the research outcomes.
The recently concluded I P I task on designing a PPI strategic plan for a clinical trial provides a lesson on one of the ways we can develop the evidence base for measuring the impact of PPI in research. By analysing PPI in a study, laying out action items and evaluating their impacts at different stages - using both qualitative and quantitative methods - we could come up with further evidence to support PPI in research.
The particular task called for highlighting the need to convince researchers on the crucial importance of PPI, where necessary; and to appropriately orient patients and educate the local community on PPI. Such scenarios could yield opportunities to develop the evidence base on PPI.