Article

A review of reviews exploring patient and public involvement in population health research

2022-11-16

Abstract excerpt

<h4>Introduction</h4> Patient and public involvement (PPI) is increasingly seen as something that is integral to research and of importance to research funders. There is general recognition that PPI is the right thing to do for both moral and practical reasons. The aim of this review of reviews is to examine how PPI can be done ‘properly’ by looking at the evidence that exists from published reviews and assessing...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: e628e503-12e9-50dc-8870-aef34442fe96
DOI: 10.1101/2022.11.16.22282319

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

A review of reviews exploring patient and public involvement in population health researchDOI 10.1101/2022.11.16.22282319Read

A review of reviews exploring patient and public involvement in population health researchSemantic proximity Read

Incorporating and Evaluating Citizen Engagement in Health Research: a Scoping Review ProtocolSemantic proximity Read

Involving patients and publics in medical and health care research studies: an exploratory survey on participant recruiting and representativeness from the perspective of study authorsSemantic proximity Read

The “PPI Hawker”: An innovative method for Patient and Public Involvement (PPI) in health researchSemantic proximity Read

“I am there just to get on with it”: a qualitative study on the labour of the patient and public involvement workforceSemantic proximity Read

Patient and public involvement in stroke research: a scoping review protocolSemantic proximity Read

Involving the public in research prioritisation and as research partners in the Wales COVID-19 Evidence Centre (2021-23): processes, research priorities, outputs, and lessonsSemantic proximity Read

“I’ve never been asked”: Community perspectives on involvement in genomics researchSemantic proximity Read

Describing the evidence-base for research engagement by health care providers and health care organisations: a scoping review.Semantic proximity Read

A multi-sited ethnography of patient and public involvement in epilepsy researchSemantic proximity Read

The Impact of Patient Engagement on Trials and Trialists in Ontario, Canada: an Interview Study With IMPACT AwardeesSemantic proximity Read

Public involvement in health genomics: the reality behind the policiesSemantic proximity Read