Results 11 to 20 of about 725,840 (314)
Plain English summary The way we collect and use patient experience data is important because of concern that patients and carers may be excluded by the limited ways it is currently done in NHS services.
Nicola Small +7 more
doaj +1 more source
Maternal mental health: a key area for future research among women with congenital heart disease
In this viewpoint, we respond to the recently published national priorities for research in congenital heart disease (CHD) among adults, established through the James Lind Alliance Priority Setting Partnership, with specific attention to priority 3 ...
Paul F Clift +12 more
doaj +1 more source
Academic researchers are increasingly asked to engage with the wider world, both in terms of creating impact from their work, and in telling the world what goes on in university research departments.
Anonymous Members of the Peninsula Public Involvement Group +2 more
doaj +1 more source
Involving the public in research [PDF]
Patient and public involvement (PPI) in research is a rapidly developing initiative across biomedicine. It recognises that in addition to being the subjects of research, patients, the public and other users have an important contribution to make to the development, quality and relevance of research and to be advocates for oral health research.
openaire +2 more sources
Correction to: Abstracts from the NIHR INVOLVE Conference 2017
Correction After publication of this supplement [1], it was brought to our attention that errors were apparent in the following abstracts and are included in this correction.
Elspeth Mathie +11 more
doaj +1 more source
The public and patient involvement imperative in Ireland: Building on policy drivers
What can we learn from the history of Public and Patient Involvement (PPI) in healthcare and research across global jurisdictions? Depending on region and context, the terminology and heritage of involvement in research vary.
Meghan Gilfoyle +9 more
doaj +1 more source
Regional working in the East of England: using the UK National Standards for Public Involvement
Plain English summary Involving patients and members of the public to help shape and carry out research is recommended in health research in the United Kingdom (UK).
Elspeth Mathie +6 more
doaj +1 more source
Introduction Many people with Parkinson’s (PwP) are not given the opportunity or do not have adequate access to participate in clinical research. To address this, we have codeveloped with users an online platform that connects PwP to clinical studies in ...
Stephen Mullin +8 more
doaj +1 more source
A Quantitative Text Analysis of the Minutes from the Meetings in Public Involvement: A Case of a Bridge Project in Cambodia [PDF]
Previous studies of public involvement in environmental impact assessment were mainly analyzed qualitatively, but quantitative text analysis is developing and being applied to social research.
Huang, Guangwei +3 more
core +1 more source
Innovative Patient Involvement During Covid-19: Keeping Patients at the Heart of HTA
The COVID-19 pandemic and lockdown measures in the United Kingdom resulted in significant challenges and created opportunities for innovation to keep patients at the heart of HTA.
Mark Rasburn +6 more
doaj +1 more source

