Patient-Public Involvement groups ensure that the voices of service users, patients, carers, care staff and the wider public are included at all stages of a research project, from design, to delivery, and disseminating the results.
The National Institute for Health Research (NIHR) defines public involvement in research as “Research being carried out ‘with’ or ‘by’ members of the public rather than ‘to’, ‘about’ or ‘for’ them.” People who join PPI groups bring their experiences, knowledge, and skills to help shape and strengthen research that really matters and makes a positive difference for those who are most affected.
The NELFT Research & Development team believe PPI involvement is vital to plan and deliver research that is high-quality, relevant, valuable, feasible and focusses on the unique needs of the communities we work with.
Our PPI groups work with our research teams and grant applicants in a range of ways. They can assist in highlighting research needs and opportunities that influence the design and delivery of a research study to improve care and practice. They may also help us identify ways to reach potential participants for a study or advise on accessibility or acceptability of study documents (such as Participant Information Sheets or adverts). Their voices are key at all stages of the research cycle to ensure we are meeting research priorities and influencing the delivery of research with the needs and views of those it will impact most at heart.
The National Institute of Health Research (NIHR) have published UK standards for public involvement in research that describe their vision of what good public involvement looks like. Read more about the six value-based themes here.
If you recognise the value of research and would like to contribute to our on-going work through PPI then please get in touch.