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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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Researcher-initiated role play, stimulated recall interview, storycrafting, painting and drawing as research methods to reach children's perspectives in health sciences

Journal of advanced nursing, 2024-07, Vol.80 (7), p.2988-3001

2024

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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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The inclusion of adults with intellectual disabilities in health research – challenges, barriers and opportunities: a mixed‐method study among stakeholders in England

Journal of intellectual disability research, 2024-02, Vol.68 (2), p.140-149

2024

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Co‐research with adults with intellectual disability: A systematic review

Journal of applied research in intellectual disabilities, 2018-09, Vol.31 (5), p.669-686

2018

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Phenomenography: A useful methodology for midwifery research

Journal of advanced nursing, 2024-06, Vol.80 (6), p.2598-2610

2024

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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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Lack of Strategic Funding and Long-Term Job Security Threaten to Have Profound Effects on Cardiovascular Researcher Retention in Australia

Heart, lung & circulation, 2020-11, Vol.29 (11), p.1588-1595

2020

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A survey study of the attitudes and experiences of adults with intellectual disability regarding participation in research

Journal of intellectual disability research, 2021-10, Vol.65 (10), p.941-948

2021

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Coproduction and health: Public and clinicians’ perceptions of the barriers and facilitators

Health expectations : an international journal of public participation in health care and health policy, 2019-02, Vol.22 (1), p.93-101

2019

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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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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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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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Why do pregnant women participate in research? A patient participation investigation using Q‐Methodology

Health expectations : an international journal of public participation in health care and health policy, 2017-04, Vol.20 (2), p.188-197

2017

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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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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

Researcher-initiated role play, stimulated recall interview, storycrafting, painting and drawing as research methods to reach children's perspectives in health sciences

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

The inclusion of adults with intellectual disabilities in health research – challenges, barriers and opportunities: a mixed‐method study among stakeholders in England

Co‐research with adults with intellectual disability: A systematic review

Phenomenography: A useful methodology for midwifery research

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

Lack of Strategic Funding and Long-Term Job Security Threaten to Have Profound Effects on Cardiovascular Researcher Retention in Australia

A survey study of the attitudes and experiences of adults with intellectual disability regarding participation in research

Coproduction and health: Public and clinicians’ perceptions of the barriers and facilitators

Responding to healthcare distrust among underserved communities: Phase II

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

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

Why do pregnant women participate in research? A patient participation investigation using Q‐Methodology

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

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