Handbook of Service User Involvement in Mental Health Research
Produktdetaljer
Biografisk notat
Jan Wallcraft is manager of the Service User Research Group for England (SURGE). She has been a leading member of the survivor/service user movement for many years and has contributed to a number of publications, e.g. “On Our Own Terms: a report on the mental health service user movement”; “Being There In A Crisis”, and “Social Perspectives in Mental Health”.
Beate Schrank has also worked for SURGE and has published on the concept of recovery in schizophrenia and on the use of the internet by people with schizophrenia.
Michaela Amering is internationally acknowledged in the field of public mental health and mental health policy. She has published on psychoeducation, informal carers (relatives), psychiatric advance directives and gender issues in mental health care, and has recently published a book on the ‘recovery perspective’ and its relevance in the care for people with psychosis. She has worked on user involvement issues in different countries and mental health care settings. She is secretary of the World Psychiatric Association Committee on Mental Health Policy. The English translation of her book on Recovery in Mental Health will also be published in March 2009.
All three editors have an impressive track record in the field of user involvement in mental health care.
<p>“Anyone involved or wanting to become involved in service user involvement in research would find plenty to inspire and challenge in this book.” (<i>Nursing Times</i>, 17 September 2012)</p> <p>"The emphasis in the handbook is of recovery and for research to be purposeful and useful in supporting this ... Reading this as a service user/carer, it gives optimism and hope as there are many good examples of personal stories and recovery – including recovery from schizophrenia which sends out a strong message." (MHRN newsletter, July 2011)</p> <p>"This engaging, helpful and well-informed handbook offers a comprehensive and thorough revievw of service user involvement in mental health research, covering issues ranging from values and collaboration to control and power." (Mental Health Practice, 1 June 2011)</p> <p>"The book may be of interest to those wanting to understand what user involvement can mean as well as those who have experienced it and want to extend their knowledge and research skills. Its scope means that chapters are necessarily brief but references are provided to follow up on interesting debates and topics." (British Journal of Psychiatry, December 2010)</p> <p>"My perspective, as a researcher who works with service users, is that this is a useful resource to dip in and out of for advice about practical issues that arise when working with service users, e.g. payment. The book clearly explains what needs to be considered in paying service users. I found this advice was not readily available elsewhere when I needed it." (The Bridge Newsletter, 2011)</p> <p> </p>
In recent years, the need for patient and public involvement in medical research has been accepted around the world. Patient groups are gaining power and demanding their right to influence the direction of research, while funding bodies are increasingly regarding patient involvement as a requirement for grant applications. However, current knowledge on how to involve service users in mental health research is sparse and dispersed. This book provides clear guidance on best practice in this area, with practical advice based on experience in countries around the world.
Handbook of Service User Involvement in Mental Health Research describes the background and principles underlying the concept of service user involvement in mental health research; it provides relevant practical advice on how to engage with service users and how to build and maintain research collaboration on a professional level. The book highlights common practical problems in service user involvement, suggesting ways to avoid pitfalls and common difficulties.
- Combines the theoretical aspects of service user involvement in research with specific examples, as well as with general practical guidelines
- Represents the views of service users, in a powerful combination with the views of other mental health professionals
- Considers the different perspectives and needs of the stakeholders concerned
- Includes a step by step guide on best practice in successful service user involvement.
Handbook of Service User Involvement in Mental Health Research is written for psychiatrists and other medical professionals managing people with psychiatric disorders, as well as for researchers in the mental health field who want to develop projects with service user involvement. It is vital reading for funding bodies requesting service user involvement, and – importantly – is written for those service users who are interested in becoming involved in research.
Preface.
About the Editors.
About the Authors.
Chapter 1 History, Context and Language (Jan Wallcraft and Mary Nettle).
Chapter 2 Principles and Motives (Alison Faulkner).
Chapter 3 Levels and Stages (Angela Sweeney and Louise Morgan).
Chapter 4 Values (Bill (KWM) Fulford and Jan Wallcraft).
Chapter 5 Roles (Jasna Russo and Peter Stastny).
Chapter 6 Capacity-building (Kim Hopper and Alisa Lincoln).
Chapter 7 Purposes and Goals (Larry Davidson, Priscilla Ridgway, Timothy Schmutte and Maria O'Connell).
Chapter 8 Topics (Paulo Del vecchio and Crystal R. Blyler).
Chapter 9 Methods (Jean Campbell).
Chapter 10 Service Users as Paid Researchers (Jonathan Delman and Alisa Lincoln).
Chapter 11 Consultation (Virginia Minogue).
Chapter 12 Collaboration (Diana Rose).
Chapter 13 Control (Peter Beresford).
Chapter 14 Power (Paddy McGowan, Liam Mac Gabhann, Chris Stevenson and Jim Walsh).
Chapter 15 Money (Sarah Hamilton).
Chapter 16 Politics (Daniel B. Fisher).
Chapter 17 Good Practice Guidance (Beate Schrank and Jan Wallcraft).
Index.
In recent years, the need for patient and public involvement in medical research has been accepted around the world. Patient groups are gaining power and demanding their right to influence the direction of research, while funding bodies are increasingly regarding patient involvement as a requirement for grant applications. However, current knowledge on how to involve service users in mental health research is sparse and dispersed. This book provides clear guidance on best practice in this area, with practical advice based on experience in countries around the world.
Handbook of Service User Involvement in Mental Health Research describes the background and principles underlying the concept of service user involvement in mental health research; it provides relevant practical advice on how to engage with service users and how to build and maintain research collaboration on a professional level. The book highlights common practical problems in service user involvement, suggesting ways to avoid pitfalls and common difficulties.
- Combines the theoretical aspects of service user involvement in research with specific examples, as well as with general practical guidelines
- Represents the views of service users, in a powerful combination with the views of other mental health professionals
- Considers the different perspectives and needs of the stakeholders concerned
- Includes a step by step guide on best practice in successful service user involvement.
Handbook of Service User Involvement in Mental Health Research is written for psychiatrists and other medical professionals managing people with psychiatric disorders, as well as for researchers in the mental health field who want to develop projects with service user involvement. It is vital reading for funding bodies requesting service user involvement, and – importantly – is written for those service users who are interested in becoming involved in research.
Produktdetaljer
Biografisk notat
Jan Wallcraft is manager of the Service User Research Group for England (SURGE). She has been a leading member of the survivor/service user movement for many years and has contributed to a number of publications, e.g. “On Our Own Terms: a report on the mental health service user movement”; “Being There In A Crisis”, and “Social Perspectives in Mental Health”.
Beate Schrank has also worked for SURGE and has published on the concept of recovery in schizophrenia and on the use of the internet by people with schizophrenia.
Michaela Amering is internationally acknowledged in the field of public mental health and mental health policy. She has published on psychoeducation, informal carers (relatives), psychiatric advance directives and gender issues in mental health care, and has recently published a book on the ‘recovery perspective’ and its relevance in the care for people with psychosis. She has worked on user involvement issues in different countries and mental health care settings. She is secretary of the World Psychiatric Association Committee on Mental Health Policy. The English translation of her book on Recovery in Mental Health will also be published in March 2009.
All three editors have an impressive track record in the field of user involvement in mental health care.