Oxford Trauma and Emergency Care
What is the James Lind Alliance?
The National Institute for Health Research (NIHR) funds the infrastructure of the James Lind Alliance (JLA) to oversee the processes for Priority Setting Partnerships (PSPs). More information can be found at http://www.jla.nihr.ac.uk/.
How did the Partnership come about?
This PSP came together in collaboration with AOUK and the Orthopaedic Trauma Society.
We approached the James Lind Alliance, who are providing expertise in PSP methodology.
Who is involved in the Partnership?
Organisations and individuals have been invited to join the PSP representing the following groups:
Can other organisations still get involved?
We need to make sure that people know about the opportunity to take part in the national surveys and learn about the results of the project, and that funders are made aware of the Top 10 priorities. You can help by promoting the surveys and, at the end of the project, disseminating the report.
How can organisations and the public find out more?
For more information or to get involved, email the Chris Bretherton at the University of Oxford, Christopher.firstname.lastname@example.org
What do you hope to achieve?
We hope to identify the unanswered questions about complex fractures from patients, carers and clinical perspectives and then prioritise those that all three groups agree are the most important. Our objectives are to:
How long will the project take?
We hope to have finished by Late 2020
How many survey responses are you hoping for?
As many as possible. Previous PSP surveys in other fields have achieved anything from a few hundred responses to several thousand.
Is my survey responses confidential?
The information that you give will be anonymised (so your name will not be published and you will not be able to be identified from what you have told us).
How is research currently funded and prioritised?
Researchers and research funders predominantly determine which areas are researched. Often this is done with reference to current literature – to identify where the gaps in knowledge are. This is sometimes done with input from patients, carers, and health and social care professionals – although never in such a thorough and systematic way as will be achieved through this partnership. The PSP process will uniquely combine the input of patients, carers and clinicians with a search of the literature.
What are the "Top 10" research priorities?
These will emerge from an interim prioritisation survey and subsequently a final workshop.
What will happen to the "Top 10" questions?
The “Top 10” questions will be publicised and discussed at events where research funders will attend. The PSP will work with its stakeholders and Partners to raise awareness of the priorities and try to get them funded as research projects. The questions will be considered by the National Institute of Health Research (NIHR) and other funding organisations when commissioning research.