Patient and Public Involvement in Health and Social Care Research

Zusatztext

This book provides a comprehensive overview of the latest theory and practice on Patient and Public Involvement (PPI) in research. Its seven chapters cover the historical and conceptual background; the various ways implementation can be approached and how they are put into practice; ethical considerations and critical perspectives, including on the potentially negative impacts of PPI; approaches to meaningful evaluation; a step by-step guide to planning PPI and conclusions with considerations for future research. Drawing on current literature, this book provides an essential reference work for research students and all who want to better understand PPI in practice. It offers exercises to address key questions, case examples and a checklist for planning PPI and includes a valuable glossary of terms.

Autorenportrait

<p><b>Jurgen Grotz</b>, PhD, is the Director of the Institute for Volunteering Research (IVR) at the University of East Anglia, UK. He has co-edited the <i>Palgrave Handbook of Volunteering, Civic Participation, and Nonprofit Associations</i> (2016).</p> <p><b>Mary Ledgard</b> is a retired researcher who has served as a trustee of Healthwatch Norfolk, UK, and is currently a PPI representative in the fields of health and social care. </p> <p><b>Fiona Poland</b> is Professor of Social Research Methodology at the University of East Anglia, UK and has worked for many years to promote inclusive community research. She is journal editor of <i>Quality in Ageing and Older Adults</i>. </p>

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