Patient And Public Involvement In Health And Social Care Research PDF Download

Are you looking for read ebook online? Search for your book and save it on your Kindle device, PC, phones or tablets. Download Patient And Public Involvement In Health And Social Care Research PDF full book. Access full book title Patient And Public Involvement In Health And Social Care Research.

Patient and Public Involvement in Health and Social Care Research

Patient and Public Involvement in Health and Social Care Research
Author: Jurgen Grotz
Publisher: Palgrave Macmillan
Total Pages: 163
Release: 2021-11-19
Genre: Social Science
ISBN: 9783030552916

Download Patient and Public Involvement in Health and Social Care Research Book in PDF, ePub and Kindle

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.


Patient and Public Involvement in Health and Social Care Research

Patient and Public Involvement in Health and Social Care Research
Author: Jurgen Grotz
Publisher: Palgrave Macmillan
Total Pages: 163
Release: 2020-12-07
Genre: Social Science
ISBN: 9783030552886

Download Patient and Public Involvement in Health and Social Care Research Book in PDF, ePub and Kindle

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.


Achieving Person-Centred Health Systems

Achieving Person-Centred Health Systems
Author: Ellen Nolte
Publisher: Cambridge University Press
Total Pages: 421
Release: 2020-08-06
Genre: Political Science
ISBN: 1108803725

Download Achieving Person-Centred Health Systems Book in PDF, ePub and Kindle

The idea of person-centred health systems is widely advocated in political and policy declarations to better address health system challenges. A person-centred approach is advocated on political, ethical and instrumental grounds and believed to benefit service users, health professionals and the health system more broadly. However, there is continuing debate about the strategies that are available and effective to promote and implement 'person-centred' approaches. This book brings together the world's leading experts in the field to present the evidence base and analyse current challenges and issues. It examines 'person-centredness' from the different roles people take in health systems, as individual service users, care managers, taxpayers or active citizens. The evidence presented will not only provide invaluable policy advice to practitioners and policymakers working on the design and implementation of person-centred health systems but will also be an excellent resource for academics and graduate students researching health systems in Europe. This title is available as Open Access on Cambridge Core.


A research handbook for patient and public involvement researchers

A research handbook for patient and public involvement researchers
Author: Penny Bee
Publisher: Manchester University Press
Total Pages: 145
Release: 2018-10-01
Genre: Science
ISBN: 152613652X

Download A research handbook for patient and public involvement researchers Book in PDF, ePub and Kindle

This electronic version has been made available under a Creative Commons (BY-NC-ND) open access license. This book is written for patients and members of the public who want to understand more about the approaches, methods and language used by health-services researchers. Patient and public involvement (PPI) in research is now a requirement of most major health-research programmes, and this book is designed to equip these individuals with the knowledge and skills necessary for meaningful participation. Edited by award-winning mental-health researchers, the book has been produced in partnership with mental-health-service users and carers with experience of research involvement. It includes personal reflections from these individuals alongside detailed information on quantitative, qualitative and health-economics research methods.


Beyond the HIPAA Privacy Rule

Beyond the HIPAA Privacy Rule
Author: Institute of Medicine
Publisher: National Academies Press
Total Pages: 334
Release: 2009-03-24
Genre: Computers
ISBN: 0309124999

Download Beyond the HIPAA Privacy Rule Book in PDF, ePub and Kindle

In the realm of health care, privacy protections are needed to preserve patients' dignity and prevent possible harms. Ten years ago, to address these concerns as well as set guidelines for ethical health research, Congress called for a set of federal standards now known as the HIPAA Privacy Rule. In its 2009 report, Beyond the HIPAA Privacy Rule: Enhancing Privacy, Improving Health Through Research, the Institute of Medicine's Committee on Health Research and the Privacy of Health Information concludes that the HIPAA Privacy Rule does not protect privacy as well as it should, and that it impedes important health research.


Equity and excellence:

Equity and excellence:
Author: Great Britain: Department of Health
Publisher: The Stationery Office
Total Pages: 64
Release: 2010-07-12
Genre: Medical
ISBN: 9780101788120

Download Equity and excellence: Book in PDF, ePub and Kindle

Equity and Excellence : Liberating the NHS: Presented to Parliament by the Secretary of State for Health by Command of Her Majesty


Patient and Public Involvement Toolkit

Patient and Public Involvement Toolkit
Author: Julia Cartwright
Publisher: John Wiley & Sons
Total Pages: 117
Release: 2011-07-05
Genre: Medical
ISBN: 1444348221

Download Patient and Public Involvement Toolkit Book in PDF, ePub and Kindle

Providing information to implement a new core healthcare requirement – patient involvement Including real case scenarios to illustrate the principles of effective PPI Following the unique Toolkit series format of flowcharts and layouts that guide the reader through each section


Participatory Health Research

Participatory Health Research
Author: Michael T. Wright
Publisher: Springer
Total Pages: 278
Release: 2018-10-10
Genre: Medical
ISBN: 3319921770

Download Participatory Health Research Book in PDF, ePub and Kindle

This groundbreaking resource explores core issues in participatory health research (PHR) and traces its global emergence as a force for improving health and well-being, healthcare services, and quality of life. The PHR approach is defined as including community members, health practitioners, and decision-makers as co-researchers, using local knowledge to reduce disparities in care, advocate for responsive health policy, and accelerate positive change in society as a whole. The book’s first half surveys themes essential to the development of the field, including evaluating PHR projects, training professionals in conducting PHR, and the ambitious work of the International Collaboration for Participatory Health Research. International perspectives showcase the varied roles of PHR in addressing urgent local health problems in their specific public health and sociocultural contexts. Among the topics covered: Demonstrating impact in participatory health research Reviewing the effectiveness of participatory health research: challenges and possible solutions Kids in Action—participatory health research with children Participatory health research: an Indian perspective Participatory health research in Latin America: scientific production on chronic diseases Participatory health research in North America: from community engagement to evidence-informed practice Participatory Health Research benefits those teaching and learning about participatory health research at institutions of higher education and in community settings, addressing diverse fields including health promotion and disease prevention, medicine and public health, quality of life, social work, and community development.


Patient Involvement in Health Technology Assessment

Patient Involvement in Health Technology Assessment
Author: Karen M. Facey
Publisher: Springer
Total Pages: 431
Release: 2017-05-15
Genre: Medical
ISBN: 9811040680

Download Patient Involvement in Health Technology Assessment Book in PDF, ePub and Kindle

This is the first book to offer a comprehensive guide to involving patients in health technology assessment (HTA). Defining patient involvement as patient participation in the HTA process and research into patient aspects, this book includes detailed explanations of approaches to participation and research, as well as case studies. Patient Involvement in HTA enables researchers, postgraduate students, HTA professionals and experts in the HTA community to study these complementary ways of taking account of patients’ knowledge, experiences, needs and preferences. Part I includes chapters discussing the ethical rationale, terminology, patient-based evidence, participation and patient input. Part II sets out methodology including: Qualitative Evidence Synthesis, Discrete Choice Experiments, Analytical Hierarchy Processes, Ethnographic Fieldwork, Deliberative Methods, Social Media Analysis, Patient-Reported Outcome Measures, patients as collaborative research partners and evaluation. Part III contains 15 case studies setting out current activities by HTA bodies on five continents, health technology developers and patient organisations. Each part includes discussion chapters from leading experts in patient involvement. A final chapter reflects on the need to clearly define the goals for patient involvement within the context of the HTA to identify the optimal approach. With cohesive contributions from more than 80 authors from a variety of disciplines around the globe, it is hoped this book will serve as a catalyst for collaboration to further develop patient involvement to improve HTA. "If you’re not involving patients, you're not doing HTA!" - Dr. Brian O’Rourke, President and CEO of CADTH, Chair of INAHTA