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Achieving Research Impact Through Co-creation in Community-Based Health Services: Literature Review and Case Study

The Milbank quarterly, 2016-06, Vol.94 (2), p.392-429

2016

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Community-Academic Partnerships: A Systematic Review of the State of the Literature and Recommendations for Future Research

The Milbank quarterly, 2016-03, Vol.94 (1), p.163-214

2016

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Uncovering the Benefits of Participatory Research: Implications of a Realist Review for Health Research and Practice

The Milbank quarterly, 2012-06, Vol.90 (2), p.311-346

2012

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Can the impact of public involvement on research be evaluated? A mixed methods study

Health expectations : an international journal of public participation in health care and health policy, 2012-09, Vol.15 (3), p.229-241

2012

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What motivates patients and caregivers to engage in health research and how engagement affects their lives: Qualitative survey findings

Health expectations : an international journal of public participation in health care and health policy, 2020-04, Vol.23 (2), p.328-336

2020

Volltextzugriff (PDF)

Health researchers' attitudes towards public involvement in health research

Health expectations : an international journal of public participation in health care and health policy, 2009-06, Vol.12 (2), p.209-220

2009

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Embedding patient and public involvement: Managing tacit and explicit expectations

Health expectations : an international journal of public participation in health care and health policy, 2019-12, Vol.22 (6), p.1231-1239

2019

Volltextzugriff (PDF)

Burdens on Research Imposed by Institutional Review Boards: The State of the Evidence and Its Implications for Regulatory Reform

The Milbank quarterly, 2011-12, Vol.89 (4), p.599-627

2011

Volltextzugriff (PDF)

Laying the groundwork: Building relationships for public and patient involvement in pre‐clinical paediatric research

Health expectations : an international journal of public participation in health care and health policy, 2020-02, Vol.23 (1), p.96-105

2020

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“About sixty per cent I want to do it”: Health researchers’ attitudes to, and experiences of, patient and public involvement (PPI)—A qualitative interview study

Health expectations : an international journal of public participation in health care and health policy, 2019-08, Vol.22 (4), p.721-730

2019

Volltextzugriff (PDF)

Codesigning person‐centred quality indicators with diverse communities: A qualitative patient engagement study

Health expectations : an international journal of public participation in health care and health policy, 2022-10, Vol.25 (5), p.2188-2202

2022

Volltextzugriff (PDF)

The power of symbolic capital in patient and public involvement in health research

Health expectations : an international journal of public participation in health care and health policy, 2017-10, Vol.20 (5), p.836-844

2017

Volltextzugriff (PDF)

Mapping the impact of patient and public involvement on health and social care research: a systematic review

Health expectations : an international journal of public participation in health care and health policy, 2014-10, Vol.17 (5), p.637-650

2014

Volltextzugriff (PDF)

Detecting, Preventing, and Responding to "Fraudsters" in Internet Research: Ethics and Tradeoffs

The Journal of law, medicine & ethics, 2015-03, Vol.43 (1), p.116-133

2015

Volltextzugriff (PDF)

Walking together: Relational Yarning as a mechanism to ensure meaningful and ethical Indigenous oral health research in Australia

Australian and New Zealand journal of public health, 2022-06, Vol.46 (3), p.354-360

2022

Volltextzugriff (PDF)

Evaluating community deliberations about health research priorities

Health expectations : an international journal of public participation in health care and health policy, 2019-08, Vol.22 (4), p.772-784

2019

Volltextzugriff (PDF)

Unregulated Health Research Using Mobile Devices: Ethical Considerations and Policy Recommendations

The Journal of law, medicine & ethics, 2020-03, Vol.48 (1_suppl), p.196-226

2020

Volltextzugriff (PDF)

‘We are the eyes and ears of researchers and community’: Understanding the role of community advisory groups in representing researchers and communities in Malawi

Developing world bioethics, 2018-12, Vol.18 (4), p.420-428

2018

Volltextzugriff (PDF)

Identifying and evaluating layers of vulnerability – a way forward

Developing world bioethics, 2019-06, Vol.19 (2), p.86-95

Luna, Florencia

2019

Volltextzugriff (PDF)

Real Ways of Working Together: co‐creating meaningful Aboriginal community consultations to advance kidney care

Australian and New Zealand journal of public health, 2022-10, Vol.46 (5), p.614-621

2022

Volltextzugriff (PDF)

Knowledge Transfer and Exchange: Review and Synthesis of the Literature

The Milbank quarterly, 2007-12, Vol.85 (4), p.729-768

2007

Volltextzugriff (PDF)

Close to the bench as well as at the bedside: involving service users in all phases of translational research

Health expectations : an international journal of public participation in health care and health policy, 2012-12, Vol.15 (4), p.389-400

2012

Volltextzugriff (PDF)

How Can Research Organizations More Effectively Transfer Research Knowledge to Decision Makers?

The Milbank quarterly, 2003-01, Vol.81 (2), p.221-248

2003

Volltextzugriff (PDF)

‘Dignity and respect’: An example of service user leadership and co‐production in mental health research

Health expectations : an international journal of public participation in health care and health policy, 2021-05, Vol.24 (S1), p.10-19

2021

Volltextzugriff (PDF)

The Structure of Clinical Translation: Efficiency, Information, and Ethics

The Hastings Center report, 2015-03, Vol.45 (2), p.27-39

2015

Volltextzugriff (PDF)

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Achieving Research Impact Through Co-creation in Community-Based Health Services: Literature Review and Case Study

Community-Academic Partnerships: A Systematic Review of the State of the Literature and Recommendations for Future Research

Uncovering the Benefits of Participatory Research: Implications of a Realist Review for Health Research and Practice

Can the impact of public involvement on research be evaluated? A mixed methods study

What motivates patients and caregivers to engage in health research and how engagement affects their lives: Qualitative survey findings

Health researchers' attitudes towards public involvement in health research

Embedding patient and public involvement: Managing tacit and explicit expectations

Burdens on Research Imposed by Institutional Review Boards: The State of the Evidence and Its Implications for Regulatory Reform

Laying the groundwork: Building relationships for public and patient involvement in pre‐clinical paediatric research

“About sixty per cent I want to do it”: Health researchers’ attitudes to, and experiences of, patient and public involvement (PPI)—A qualitative interview study

Codesigning person‐centred quality indicators with diverse communities: A qualitative patient engagement study

The power of symbolic capital in patient and public involvement in health research

Mapping the impact of patient and public involvement on health and social care research: a systematic review

Detecting, Preventing, and Responding to "Fraudsters" in Internet Research: Ethics and Tradeoffs

Walking together: Relational Yarning as a mechanism to ensure meaningful and ethical Indigenous oral health research in Australia

Evaluating community deliberations about health research priorities

Unregulated Health Research Using Mobile Devices: Ethical Considerations and Policy Recommendations

‘We are the eyes and ears of researchers and community’: Understanding the role of community advisory groups in representing researchers and communities in Malawi

Identifying and evaluating layers of vulnerability – a way forward

Real Ways of Working Together: co‐creating meaningful Aboriginal community consultations to advance kidney care

Knowledge Transfer and Exchange: Review and Synthesis of the Literature

Close to the bench as well as at the bedside: involving service users in all phases of translational research

How Can Research Organizations More Effectively Transfer Research Knowledge to Decision Makers?

‘Dignity and respect’: An example of service user leadership and co‐production in mental health research

The Structure of Clinical Translation: Efficiency, Information, and Ethics

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