Results 21 to 30 of about 411,635 (248)
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
Becoming part of behind the scenes: patients' experiences of co-learning with primary health care teams. [PDF]
Current debates about the involvement of health service users in service delivery, research and education focus on the purpose of their involvement, the methods of their involvement, barriers to their involvement and the impact of their involvement ...
Worswick, Louise
core +6 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
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 +7 more
doaj +1 more source
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 +13 more
doaj +1 more source
PANDA: A case-study examining a successful Audiology and Otology Patient and Public Involvement and Engagement research group [PDF]
There has been increasing involvement of patients and members of the public in research; however, case studies describing patient research groups with hearing loss are non-existent. Such case studies will be valuable, enabling evidence-based dialogue and
Richard Allen +11 more
core +1 more source
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 +10 more
doaj +1 more source
Exploring the Multidimensionality of Trust in Participatory Health Partnerships - A Network Approach
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 +7 more
doaj +1 more source
ReseArch with Patient and Public invOlvement: a RealisT evaluation - the RAPPORT study [PDF]
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. +36 more
core +2 more sources
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 +9 more
doaj +1 more source

