Ahead of Cochrane Colloquium Edinburgh 2018, which will be a #PatientsIncluded event, Sarah Chapman was invited by The BMJ to write an Opinion Piece about co-producing conferences with patients. She reflects on the recent #BMJDebate about the issue. This article was originally published on BMJ Opinion.
Tag Archives: patient and public involvement
Katie Gillies and Derek Stewart, from the PRioRiTy II group, highlight the need for the identification of a national research agenda on retention to clinical trials developed and prioritised by all relevant stakeholders.
On World Asthma Day, Emma Dennett from Cochrane Airways blogs about a workshop held to explore what matters to people with asthma and so identify topics for Cochrane Reviews.
Here's what patients and carers have told us will make the 2018 Cochrane Colloquium, Cochrane For All, accessible, inclusive and interesting.
Announcing our #cochraneforall tweetchats - another opportunity to tell us what we could do to increase the involvement of patients and carers in next year's Cochrane conference.
Richard Morley and Sarah Chapman acknowledge the sensitivities around 'patient' and alternative terms, as work gets under way to make the Cochrane conference 2018 a 'Patients Included' event
Steven Williams blogs about the recently launched 'My Signals', in which health and social care staff and service users describe research that is important for them.
Announcing our plans to make the Cochrane Colloquium, our global conference, to be held in Edinburgh in 2018, a Patients Included event.
Read about Cochrane’s new citizen science platform and their fast, furious and successful their recent 48 hour citation screening challenge!
What's most important in hearing loss research and how we decided
Working out what matters most for future research. Members of the Priority Setting Partnership for mild to moderate hearing loss explain
Why patients must be involved in research and how social media can help