Results 21 to 30 of about 725,840 (314)

Talking about living and dying with the oldest old: public involvement in a study on end of life care in care homes [PDF]

, 2011
Background: Public involvement in research on sensitive subjects, such as death and dying, can help to ensure that questions are framed to reflect the interests of their peers, develop a shared understanding of issues raised, and moderate the often ...
Mendoza Alex, Cowe Marion, Diane Munday, Katherine Froggatt, Munday Diane, Iliffe Steve, Wilson, Patricia M., Froggatt Katherine, Wilson Patricia M, Stephen Barclay, Gage, Heather, Heather Gage, Crang, Clare, Barclay Stephen, Elspeth Mathie, Patricia M Wilson, Clare Crang, Goodman Claire, Mathie, Elspeth, Barclay, Stephen, Daphne Westwood, Westwood Daphne, Alex Mendoza, Crang Clare, Froggatt, Katherine, Manthorpe Jill, Munday, Diane, Marion Cowe, Cowe, Marion, Iliffe, Steve, Jill Manthorpe, Mathie Elspeth, Goodman, Claire, Goodman, Claire M., Manthorpe, Jill; id_orcid, Wilson, Patricia, Westwood, Daphne, Gage Heather, Mendoza, Alex, Claire Goodman, Manthorpe, Jill, Steve Iliffe   +41 more
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Primary care-led commissioning and public involvement in the English National Health Service. Lessons from the past. [PDF]

, 2014
Background: Patient and Public involvement (PPI) in health care occupies a central place in Western democracies. In England, this theme has been continuously prominent since the introduction of market reforms in the early 1990s.
Peckham, Stephen, Wilson, Patricia, Wilson, Patricia M., Petsoulas, Christina, Smiddy, Jane, Smiddy, J., Petsoulas, C.   +6 more
core   +1 more source

Co-creation of a complex, multicomponent rehabilitation intervention and feasibility trial protocol for the PostUraL tachycardia Syndrome Exercise (PULSE) study

Pilot and Feasibility Studies, 2023
Background There is a dearth of research to support the treatment of people with postural tachycardia syndrome (PoTS). Despite expert consensus suggesting exercise is recommended for this patient group, there are no randomised control trials examining ...
Gemma Pearce, Nikki Holliday, Harbinder Sandhu, Helen Eftekhari, Julie Bruce, Emma Timms, Laura Ablett, Lesley Kavi, Jane Simmonds, Rebecca Evans, Paul Magee, Richard Powell, Shane Keogh, Gordon McGregor   +13 more
doaj   +1 more source

ReseArch with Patient and Public invOlvement: a RealisT evaluation - the RAPPORT study [PDF]

, 2015
Background Patient and public involvement (PPI) is a prerequisite for many funding bodies and NHS research ethics approval. PPI in research is defined as research carried out with or by the public rather than to, about or for them.
Poland, F., Diane Munday, Kendall, S., Munday, D., Howe, Amanda, Goodman, C., Staniszweska, Sophie, Peckham, S., Peckham, Stephen, Stephen Peckham, McNeilly, Elaine, Wilson, P., Sally Kendall, Elspeth Mathie, Elaine McNeilly, Julia Keenan, Keenan, J., Mathie, Elspeth, Keenan, Julia, Sophie Staniszewska, Staniszewska, S., Mathie, E., Fiona Poland, Howe, A., Staniszewska, Sophie, Munday, Diane, Marion Cowe, Cowe, Marion, Goodman, Claire, Kendall, Sally, Patricia Wilson, Wilson, Patricia, Cowe, M., Claire Goodman, McNeilly, E., Poland, Fiona, Amanda Howe   +36 more
core   +1 more source

Co-creation of a Patient-Reported Outcome Measure for Older People Living with Frailty Receiving Acute Care (PROM-OPAC)

Journal of Patient Experience, 2023
Older people living with frailty emphasize autonomy and function as acute healthcare outcome goals. Existing Patient-Reported Outcome Measures (PROMs) measure function but do not comprehensively address autonomy.
James D. van Oppen MRes, Timothy J. Coats MD, Simon P. Conroy PhD, Jagruti Lalseta, Vivien Richardson, Peter Riley, Jose M. Valderas PhD, Nicola Mackintosh PhD   +7 more
doaj   +1 more source

Ethnicity recording in health and social care data collections in Ireland: where and how is it measured and what is it used for?

International Journal for Equity in Health, 2019
Background In the European Union (EU), discrimination based on racial and ethnic origin is prohibited under the Racial Equality Directive. Ireland is one of only three EU countries where a legal duty of equality data collection is placed on public bodies.
Ailish Hannigan, Nazmy Villarroel, Maria Roura, Joseph LeMaster, Alphonse Basogomba, Colette Bradley, Anne MacFarlane   +6 more
doaj   +1 more source

Personal and Public Involvement (PPI) - Consultation Scheme

, 2012
The Chief Executive is accountable to the Minister for Health, Social Services and Public Safety for the performance of the Public Health Agency and its staff.The Chief Executive is required to appoint a senior professional at Board level to provide ...
Public Health Agency
core   +1 more source

Public involvement could usefully inform ethical review, but rarely does: what are the implications?

Research Involvement and Engagement, 2017
Plain English summary Researchers carrying out research in the NHS in England have to obtain approval for their study from an NHS Research Ethics Committee (REC).
Kristina Staley, Jim Elliott
doaj   +1 more source

Reducing health inequalities through general practice: protocol for a realist review (EQUALISE)

BMJ Open, 2021
Introduction Healthcare organisations recognise the moral imperative to address inequalities in health outcomes but often lack an understanding of which types of interventions are likely to reduce them.
Geoff Wong, Clare Bambra, Anna Gkiouleka, Isla Kuhn, Annie Moseley, Sarah Sowden, Rikke Siersbaek, John Alexander Ford, Rebecca R Harmston, Fiona Head, Sukaina Manji   +10 more
doaj   +1 more source

Strategy for personal and public involvement

, 2014
Local and national policy increasingly emphasises the central role of service users and the public in shaping Health and Social Care (HSC). This is the second edition of the HSC R&D Division \u27s Personal and Public Involvement (PPI) Strategy, which ...
Public Health Agency
core   +1 more source