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Involving patients and the public in the NHS [PDF]

Clinical Medicine, 2003
Involving patients and the public in the NHS is a new strategic initiative by the Deparment of Health. Over time it will make a significant change to how services are designed and delivered. Doctors need to be aware of this new legislation and the change in the patient/clinician dynamic it embraces.
openaire   +2 more sources

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

Correction to: Abstracts from the NIHR INVOLVE Conference 2017

Research Involvement and Engagement, 2018
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, Helena Wythe, Diane Munday, Paul Millac, Graham Rhodes, Nick Roberts, Jean Simpson, Nat Barden, Penny Vicary, Amander Wellings, Fiona Poland, Julia Jones   +11 more
doaj   +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

Exploring the Multidimensionality of Trust in Participatory Health Partnerships - A Network Approach

Frontiers in Public Health, 2022
IntroductionPrevious studies have identified “trust” as a key mechanism to achieve sustainable partnerships in participatory health research, which themselves can represent social networks.
Meghan Gilfoyle, Meghan Gilfoyle, Jon Salsberg, Jon Salsberg, Miriam McCarthy, Anne MacFarlane, Anne MacFarlane, Pádraig MacCarron   +7 more
doaj   +1 more source

A systematic review and recommendations for prom instruments for older people with frailty in emergency care

Journal of Patient-Reported Outcomes, 2022
Introduction The current service metrics used to evaluate quality in emergency care do not account for specific healthcare outcome goals for older people living with frailty.
James David van Oppen, Abdullah Alshibani, Timothy John Coats, Blair Graham, Patricia Holch, Jagruti Lalseta, Nicola Mackintosh, Vivien Richardson, Peter Riley, Jose M. Valderas, Simon Paul Conroy   +10 more
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

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

Clinical service delivery implications of the COVID-19 pandemic on people with Inflammatory bowel disease: a qualitative study

BMC Health Services Research, 2023
Background During the COVID-19 pandemic, clinical services were severely disrupted, restricted, or withdrawn across the country. People living with Inflammatory Bowel Disease (IBD) – an auto-immune disorder for which medical treatment often results in ...
Karen Kemp, Pearl Avery, Ruby Bryant, Amanda Cross, Kayleigh Danter, Andrew Kneebone, Deborah Morris, Amy Walker, Lisa Whitley, Lesley Dibley   +9 more
doaj   +1 more source

Regional working in the East of England: using the UK National Standards for Public Involvement

Research Involvement and Engagement, 2018
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, Helena Wythe, Diane Munday, Graham Rhodes, Penny Vicary, Paul Millac, Julia Jones   +6 more
doaj   +1 more source