The role of Patient and public involvement (PPI) in pre-clinical spinal cord research: An interview study

Abstract

Background Patient and public involvement in research (PPI) has many benefits including increasing relevance and impact. While using PPI in clinical research is now an established practice, the involvement of patients and the public in pre-clinical research, which takes place in a laboratory setting, has been less frequently described and presents specific challenges. This study aimed to explore the perspectives of seriously injured rugby players’ who live with a spinal cord injury on PPI in pre-clinical research. Methods Semi-structured interviews were conducted via telephone with 11 seriously injured rugby players living with spinal cord injury on the island of Ireland. A purposive sampling approach was used to identify participants. Selected individuals were invited to take part via gatekeeper in a charitable organisation that supports seriously injured rugby players. Interviews were transcribed verbatim and analysed thematically. Findings Six themes were identified during analysis: ‘appreciating potential benefits of PPI despite limited knowledge’, ‘the informed perspectives of people living with spinal cord injury can improve pre-clinical research relevance’, ‘making pre-clinical research more accessible reduces the potential for misunderstandings to occur’, ‘barriers to involvement include disinterest, accessibility issues, and fear of losing hope if results are negative’, ‘personal contact and dialogue helps people feel valued in pre-clinical research, and ‘PPI can facilitate effective dissemination of pre-clinical research as desired by people living with spinal cord injury.’ Conclusion People affected by spinal cord injury in this study desire further involvement in pre-clinical spinal cord injury research through dialogue and contact with researchers. Sharing experiences of spinal cord injury can form the basis of PPI for pre-clinical spinal cord injury research.