Project

Back in February 2021, as part of early public involvement work for a postgraduate engineering project, the team first met to discuss the major factors associated with hand OA from a lived-experience perspective. These discussions highlighted the lack of knowledge and awareness of hand osteoarthritis in comparison to hip or knee osteoarthritis amongst the public and researchers. This emphasised the need for more publicly-accessible content about hand osteoarthritis from a lived-experience point of view.

INVOLVE, an advisory body established and funded by the National Institute for Health Research (NIHR), defines Patient and Public Involvement (PPI), or recently more collectively referred to as Public Involvement as research carried out ‘with; or ‘by’ members of the public rather than ‘to’, about’ or ‘for’ them. [1]
Whilst biomechanical engineering is a multidisciplinary field that encourages collaboration between engineers and healthcare professionals, research generally continues to be conducted ’on’ or ’for’ patients rather than ’with’ them; i.e. it is a discipline that remains largely technology-driven. Therefore, there is scope to incorporate more patient and public involvement practices in engineering research and show how valuable it is in developing better knowledge of and interventions for conditions, of which researchers often have no experience.
A postgraduate research project concerning the characterisation of the key clinical, biomechanical and social factors associated with hand joint diseases such as osteoarthritis (OA) aims to combine computational modelling methods and public involvement. Since incorporating PPI in their respective projects, reserachers in the school of Engineering at the University of Southampton have seen first-hand how consulting and collaborating with members of the public can help to identify and prioritise research areas as well as to build an active and equal relationship between researchers and the public.
In the early public invovlement sessions, members of the public living with hand OA addressed the lack of knowledge of hand OA compared to hip or knee OA, both amongst the general public and researchers, which emphasised the need for more information on hand OA treatment and self-management techniques. Since we have formed the ’How Would You HAND-le this’ project team, consisting of public contributors and researchers, to address these shortcomings directly by raising awareness of what it is like to live with hand OA and communicate to researchers the importance of incoporating these lived-experience insights in the development of healthcare tools or interventions.

To learn more about public invovlement in research, head over to the resource tab...