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An empirically based conceptual framework for fostering meaningful patient engagement in research

Health expectations : an international journal of public participation in health care and health policy, 2018-02, Vol.21 (1), p.396-406

2018

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Clinical research potential in Victorian hospitals: the Victorian clinician researcher needs analysis survey

Internal medicine journal, 2014-05, Vol.44 (5), p.477-482

2014

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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

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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

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Reciprocal relationships and the importance of feedback in patient and public involvement: A mixed methods study

Health expectations : an international journal of public participation in health care and health policy, 2018-10, Vol.21 (5), p.899-908

2018

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Facilitators and barriers to co‐research by people with dementia and academic researchers: Findings from a qualitative study

Health expectations : an international journal of public participation in health care and health policy, 2019-08, Vol.22 (4), p.761-771

2019

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‘Keeping it real’: A qualitative exploration of preferences of people with lived experience for participation and active involvement in mental health research in Australia

Health expectations : an international journal of public participation in health care and health policy, 2024-02, Vol.27 (1), p.e13934-n/a

2024

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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

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‘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

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Researchers' perspectives on public involvement in health research in Singapore: The argument for a community‐based approach

Health expectations : an international journal of public participation in health care and health policy, 2019-08, Vol.22 (4), p.666-675

2019

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Promoting empowerment and self‐care in older women through participatory action research: Analysis of the process of change

Journal of advanced nursing, 2023-06, Vol.79 (6), p.2224-2235

2023

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Building an Inclusive Research Team: The Importance of Team Building and Skills Training

Journal of applied research in intellectual disabilities, 2014-01, Vol.27 (1), p.13-22

2014

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Relational practices for meaningful inclusion in health research: Results of a deliberative dialogue study

Health expectations : an international journal of public participation in health care and health policy, 2024-02, Vol.27 (1), p.e13865-n/a

2024

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Patient and public involvement in preclinical and medical research: Evaluation of an established programme in a Discovery‐Based Medical Research Institute

Health expectations : an international journal of public participation in health care and health policy, 2024-02, Vol.27 (1), p.e13968-n/a

2024

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Paying patient and caregiver research participants: putting theory into practice

Journal of advanced nursing, 2017-04, Vol.73 (4), p.847-856

2017

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Patient and Public Involvement and Engagement in a doctoral research project exploring self‐harm in older adults

Health expectations : an international journal of public participation in health care and health policy, 2019-08, Vol.22 (4), p.617-631

2019

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Is it worth it? Patient and public views on the impact of their involvement in health research and its assessment: a UK‐based qualitative interview study

Health expectations : an international journal of public participation in health care and health policy, 2017-06, Vol.20 (3), p.519-528

2017

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Responding to healthcare distrust among underserved communities: Phase II

Psycho-oncology (Chichester, England), 2022-01, Vol.31 (1), p.3-8

2022

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A life‐course theory exploration of opioid‐related maternal mortality in the United States

Addiction (Abingdon, England), 2020-11, Vol.115 (11), p.2079-2088

2020

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'You need to let your voice be heard': research participants' views on research

Journal of intellectual disability research, 2013-03, Vol.57 (3), p.216-225

2013

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Factors associated with biomedical research participation within community‐based samples across 3 National Cancer Institute–designated cancer centers

Cancer, 2020-03, Vol.126 (5), p.1077-1089

2020

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The Leadership Mentoring in Nursing Research Program for Postdoctoral Nurses: A Development Paper

Journal of nursing scholarship, 2020-07, Vol.52 (4), p.435-445

2020

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Perspectives of researchers and clinicians on patient and public involvement (PPI) in preclinical spinal cord research: An interview study

Health expectations : an international journal of public participation in health care and health policy, 2024-02, Vol.27 (1), p.e13967-n/a

2024

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Nurses´ stressors and psychological distress during the COVID‐19 pandemic: The mediating role of coping and resilience

Journal of advanced nursing, 2021-03, Vol.77 (3), p.1335-1344

2021

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Data sharing in cancer research: A qualitative study exploring community members' preferences

Cancer medicine (Malden, MA), 2024-08, Vol.13 (15), p.e70084-n/a

2024

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An empirically based conceptual framework for fostering meaningful patient engagement in research

Clinical research potential in Victorian hospitals: the Victorian clinician researcher needs analysis survey

“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

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

Reciprocal relationships and the importance of feedback in patient and public involvement: A mixed methods study

Facilitators and barriers to co‐research by people with dementia and academic researchers: Findings from a qualitative study

‘Keeping it real’: A qualitative exploration of preferences of people with lived experience for participation and active involvement in mental health research in Australia

Evaluating community deliberations about health research priorities

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

Researchers' perspectives on public involvement in health research in Singapore: The argument for a community‐based approach

Promoting empowerment and self‐care in older women through participatory action research: Analysis of the process of change

Building an Inclusive Research Team: The Importance of Team Building and Skills Training

Relational practices for meaningful inclusion in health research: Results of a deliberative dialogue study

Patient and public involvement in preclinical and medical research: Evaluation of an established programme in a Discovery‐Based Medical Research Institute

Paying patient and caregiver research participants: putting theory into practice

Patient and Public Involvement and Engagement in a doctoral research project exploring self‐harm in older adults

Is it worth it? Patient and public views on the impact of their involvement in health research and its assessment: a UK‐based qualitative interview study

Responding to healthcare distrust among underserved communities: Phase II

A life‐course theory exploration of opioid‐related maternal mortality in the United States

'You need to let your voice be heard': research participants' views on research

Factors associated with biomedical research participation within community‐based samples across 3 National Cancer Institute–designated cancer centers

The Leadership Mentoring in Nursing Research Program for Postdoctoral Nurses: A Development Paper

Perspectives of researchers and clinicians on patient and public involvement (PPI) in preclinical spinal cord research: An interview study

Nurses´ stressors and psychological distress during the COVID‐19 pandemic: The mediating role of coping and resilience

Data sharing in cancer research: A qualitative study exploring community members' preferences

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