Patient and Public Involvement, aka Public Involvement (PPI)

PPI is a form of engaged research, referring to public involvement and co-production in health and social care research. It is a research practice.

The UK National Institute for Health Research defines PPI as follows: Research carried out ‘with’ or ‘by’ members of the public rather than ‘to’, ‘about’ or ‘for’ them. This may include potential patients, carers and people who use health and social care services as well as people from organizations that represent people who use services.

PPI does NOT include the recruitment of study participants; this is participation of the public rather than involvement. It also does NOT include work aimed at raising awareness of the public around research, such as media publications of research findings, and outreach activities such as open days in research facilities. This is public engagement.

PPI is an ACTIVE partnership with members of the public in the research project and can include, for example: involvement in choice of research topics; assisting in the design; advising on the research project; carrying out the research.

 Resources: 

https://www.nihr.ac.uk/documents/ppi-patient-and-public-involvement-resources-for-applicants-to-nihr-research-programmes/23437

https://recap-preterm.eu/wp-content/uploads/2021/07/A_short_guide_to_successful_patient_involvement_in_EU-funded_healthcare_research_projects_layout.pdf

 

Pyramid showing the differences between participation, engagement and involvement.

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