S
Simon Denegri
Researcher at National Institute for Health Research
Publications - 10
Citations - 1104
Simon Denegri is an academic researcher from National Institute for Health Research. The author has contributed to research in topics: Evidence-based practice & Social responsibility. The author has an hindex of 6, co-authored 9 publications receiving 670 citations. Previous affiliations of Simon Denegri include University of Southampton.
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Journal ArticleDOI
GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research
Sophie Staniszewska,Jo Brett,Iveta Simera,Kate Seers,Carole Mockford,S. Goodlad,Douglas G. Altman,David Moher,Rosemary Barber,Simon Denegri,A. R. Entwistle,Peter Littlejohns,Christopher Morris,Rashida Suleman,Victoria Thomas,Colin Tysall +15 more
TL;DR: Both versions of GRIPP2 represent the first international evidence based, consensus informed guidance for reporting patient and public involvement in research and aim to improve the quality, transparency, and consistency of the international PPI evidence base.
Journal ArticleDOI
Reviewing progress in public involvement in NIHR research: developing and implementing a new vision for the future.
TL;DR: The NIHR is the first funder of its size and importance globally to review its approach to public involvement and there is a need to consolidate progress and accelerate the spread of effective practice, drawing on evidence.
Journal ArticleDOI
Patients' roles and rights in research.
TL;DR: Full partnership with patients is essential to any modern research enterprise and in this case, it is vital to improve the quality of life for patients through informed consent and informed consent.
Journal ArticleDOI
Consensus Statement on Public Involvement and Engagement with Data-Intensive Health Research.
Mhairi Aitken,Mary P. Tully,Carol Porteous,Simon Denegri,Sarah Cunningham-Burley,Natalie Banner,Corri Black,Michael M. Burgess,Lynsey Cross,Johannes J. M. van Delden,Elizabeth Ford,Sarah Fox,Natalie K Fitzpatrick,Kay Gallacher,C. A. Goddard,Lamiece Hassan,Ron Jamieson,Kerina H. Jones,Minna Susanna Kaarakainen,Fiona Lugg-Widger,Kimberlyn McGrail,Anne McKenzie,Rosalyn Moran,Madeleine J Murtagh,Malcolm Oswald,Alison Paprica,Nicola Perrin,Emma Richards,John Rouse,Joanne Webb,Donald J. Willison +30 more
TL;DR: An international group of stakeholders with a range of expertise in public involvement and engagement (PI&E) relating to data-intensive health research sets out eight key principles to establish a secure role for PI&E in and with the research community internationally and ensure best practice in its execution.
Journal ArticleDOI
Patient and public involvement in research: future challenges
TL;DR: While PPI activity has increased, the evidence base underpinning this activity remains relatively weak, primarily because of poor reporting with many studies including only partial information.