The student patient alliance: development and formative evaluation of an initiative to support collaborations between patient and public involvement partners and doctoral students

Gwenda Simons, Rebecca Birch, Joanne Stocks, Elspeth Insch, Rob Rijckborst, Georgiana Neag, Heidi McColm, Leigh Romaniuk, Claire Wright, Bethan E. Phillips, Simon W. Jones, Arthur G. Pratt, Stefan Siebert, Karim Raza, Marie Falahee*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Background: While the integration of patient and public involvement (PPI) in clinical research is now widespread and recommended as standard practice, meaningful PPI in pre-clinical, discovery science research is more difficult to achieve. One potential way to address this is by integrating PPI into the training programmes of discovery science postgraduate doctoral students. This paper describes the development and formative evaluation of the Student Patient Alliance (SPA), a programme developed at the University of Birmingham that connects PPI partners with doctoral students.

Methods: Following a successful pilot of the SPA by the Rheumatology Research Group at the University of Birmingham, the scheme was implemented across several collaborating Versus Arthritis / Medical Research Council (MRC) centres of excellence. Doctoral students were partnered with PPI partners, provided with initial information and guidance, and then encouraged to work together on research and public engagement activities. After six months, students, their PPI partners and the PPI coordinators at each centre completed brief surveys about their participation in the SPA.

Results: Both doctoral students and their PPI partners felt that taking part in SPA had a positive impact on understanding, motivation and communication skills. Students reported an increased understanding of PPI and patient priorities and reported improved public engagement skills. Their PPI partners reported a positive impact of the collaboration with the students. They enjoyed learning about the student’s research and contributing to the student’s personal development. PPI coordinators also highlighted the benefits of the SPA, but noted some challenges they had experienced, such as difficulties matching students with PPI partners.

Conclusions: The SPA was valued by students and PPI partners, and it is likely that initiatives of this kind would enhance students’ PPI and public engagement skills and awareness of patients’ experiences on a wider scale. However, appropriate resources are needed at an institutional level to support the implementation of effective programmes of this kind on a larger scale.
Original languageEnglish
Article number36
Number of pages13
JournalBMC Rheumatology
Volume7
Issue number1
DOIs
Publication statusPublished - 3 Oct 2023

Bibliographical note

Funding:
This work was supported by the Research into Inflammatory Arthritis Centre Versus Arthritis (RACE) (grant number 22072) and the National Institute for Health and Care Research (NIHR) Birmingham Biomedical Research Centre (BRC). KR was supported by the NIHR Birmingham Biomedical Research Centre. Newcastle contributors were was supported by the NIHR Newcastle Biomedical Research Centre. The views expressed are those of the author(s) and not necessarily those of the NIHR or the Department of Health and Social Care. GN was supported by a PhD studentship from CMAR funded by the Medical Research Council and Versus Arthritis, grant number MR/K00414X/1. SWJ was supported by the Medical Research Council, grant number MR/W026961/1.

Keywords

  • Rheumatic and musculoskeletal diseases.
  • Doctoral students
  • Patient and public involvement
  • Discovery science

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