RDS North East and North Cumbria PPI Checklist: some questions to consider when beginning to develop PPI for your proposal
NIHR Public Involvement ‘Pocket’ Guide A brief guide to the role of the Research Design Service in supporting public involvement in funding applications.
The UK Public Involvement Standards Six standards and indicators for public involvement in research.
Top tips for carrying out PPI activities during COVID Some TOP TIPS designed to help researchers who are in the process of applying for grants, consider how to ensure they can continue to collaborate with public representatives in a meaningful way during these challenging and exceptional times, produced by RDS South Central.
INVOLVE is a national advisory group. It supports active public involvement in NHS, public health and social care research and has a number of resources to do that.
NIHR Increasing participation of Black Asian and Minority Ethnic (BAME) groups in health and social care research This toolkit is designed to help researchers develop more relevant research questions, consider engagement of BAME groups in a more structured way and provide tips on better participation and dissemination of research findings.
Briefing notes for researchers An online resource of ten briefing notes for researchers on how to involve members of the public in research. Includes supplementary material, case studies, and templates.
Top tips for public involvement Seven tips for successful and meaningful public involvement.
‘Making it Clear’ campaign Provides guidance for researchers and board/panel members in relation to developing a clear and concise plain English summary of research projects.
Payment and recognition for public involvement There are a number of ways to recognise the contributions of members of the public who are actively involved in research. This page links to guides and practical advice on payment and non-monetary methods for recognising the time, skills and expertise provided by members of the public.
People in Research Opportunities for public involvement in NHS, public health and social care research.
Public information pack 2018 A Public Information Pack (PIP) made up of 4 booklets, for members of the public who are interested in getting involved in health and social care research.
invoDIRECT This online resource is a directory of networks, groups and organisations that support active public involvement in NHS, public health and social care research. The resource will allow individuals or networks, groups or organisations to be aware of and make contact with others who are carrying out similar work.
Public co-applicants in research – guidance on roles and responsibilities Guidance developed jointly by the NHS R&D Forum, the Health Research Authority and INVOLVE for researchers and public contributors about the role of a public co applicant.
Involving children and young people in research: top tips and essential key issues for researchers An overview of the key issues around involving children and young people in NHS, public health and social care research.
Going the extra mile The final report and recommendations to the Director General Research and Development / Chief Medical Officer (CMO) Department of Health of the ‘Breaking Boundaries’ strategic review of public involvement in the National Institute for Health Research (NIHR).
The James Lind Alliance The James Lind Alliance (JLA) is a non-profit making initiative established in 2004. It brings patients, carers and clinicians together in Priority Setting Partnerships (PSPs) to identify and prioritise the Top 10 unanswered questions or evidence uncertainties that they agree are the most important.
VOICE is a unique organisation, comprising a large network of citizens across the UK and internationally. Members contribute immense insights, experience, ideas and vision to identify unmet needs and opportunities, to drive innovation on ageing and improve health research.
HealthWatch are an independent national champion for people who use health and social care services. Every local authority has their own HealthWatch.
Generation R A national network of Young People’s Advisory Groups (YPAGs) across the UK including YPAG North England. YPAGs promote and support the involvement of children and young people in the design and delivery of research.
A framework for public involvement at the design stage of NHS health and social care research: time to develop ethically conscious standards – Raksha Pandya-Wood, Duncan S. Barron and J. Elliott.