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Involving a black woman patient and public involvement group in maternal health methodology research: learning from the PROMISE Study [PDF]
Background Patient and public involvement (PPI) is at the centre of high-quality health research, but PPI representatives are often limited in terms of demographic diversity and are often absent from methodology research.
Sophie S. Hall +6 more
doaj +2 more sources
Background Advance care planning (ACP) is the process supporting individuals with life-limiting illness to make informed decisions about their future healthcare.
Jodie Crooks +3 more
doaj +1 more source
IntroductionCerebral palsy (CP) is a lifelong condition, where people may experience complications as they age. Including the views of people with CP through Public and Patient Involvement (PPI) ensures that research into the condition is relevant and ...
Manjula Manikandan +10 more
doaj +1 more source
Background There are many described benefits of community-based participatory research (CBPR), such as increased relevance of research for those who must act on its findings.
Meghan Gilfoyle +2 more
doaj +1 more source
Personal assistants in England and the factors associated with absenteeism
Personal assistants (PAs) have become an increasingly important element of long-term care (LTC) in England since the introduction of Direct Payments in 1996 and the Care Act 2014 legislation.
Daniel Roland +6 more
doaj +1 more source
Plain English Summary Involving patients, family carers and members of the public in research is known as patient and public involvement, or PPI. In health and social care research, PPI is considered important by many, including patients and research ...
Julia Jones +7 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
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
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
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

