Overarching Priorities for Health and Care Research in the United Kingdom: A Coproduced Synthesis of James Lind Alliance ‘Top 10s’
Journal article
Crocker JC. et al, (2024), Health Expectations, 27
Developing user personas to capture intersecting dimensions of disadvantage in older patients who are marginalised: a qualitative study.
Journal article
Husain L. et al, (2024), Br J Gen Pract
Safety implications of remote assessments for suspected COVID-19: qualitative study in UK primary care
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Wieringa S. et al, (2023), BMJ Quality and Safety, 32, 732 - 741
Co-design and its consequences: developing a shared patient engagement framework in the IMI-PARADIGM project
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Gunn C. et al, (2023), Science and Public Policy
The ecomap: a tool for extending understanding in hermeneutic phenomenological research
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Jestico ECL. et al, (2023), Nurse Researcher
Desperately Seeking the Intersectionality in Digital Health Disparities Research: Narrative Review to Inform a Richer Theorisation of Multiple Disadvantage.
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Husain L. et al, (2022), J Med Internet Res
How ‘significant others’ may support parents with decision‐making about their child’s cancer care: An integrative literature review
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Jestico ECL. et al, (2022), Journal of Clinical Nursing
Planning and Evaluating Remote Consultation Services: A New Conceptual Framework Incorporating Complexity and Practical Ethics
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Greenhalgh T. et al, (2021), Frontiers in Digital Health, 3
Could expanding the covid-19 case definition improve the UK’s pandemic response?
Other
FINLAY T. et al, (2021), BMJ: British Medical Journal
Could expanding the covid-19 case definition improve the UK's pandemic response?
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Crozier A. et al, (2021), The BMJ, 374
Evaluation of patient engagement in medicine development: A multi‐stakeholder framework with metrics
Journal article
Vat LE. et al, (2021), Health Expectations
PNS232 What Constitutes the VALUE of Patient Engagement in the Development of New Medicines? Development of the Paradigm Monitoring and Evaluation Framework
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Robinson P. et al, (2020), Value in Health, 23, S680 - S680
Evaluating the “return on patient engagement initiatives” in medicines research and development: A literature review
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Vat LE. et al, (2020), Health Expectations, 23, 5 - 18
Public involvement in the governance of population-level biomedical research: Unresolved questions and future directions
Journal article
Erikainen S. et al, (2020), Journal of Medical Ethics
WHAT CONSTITUTES THE VALUE OF PATIENT ENGAGEMENT IN THE DEVELOPMENT OF NEW MEDICINES? DEVELOPMENT OF THE PARADIGM MONITORING AND EVALUATION FRAMEWORK
Conference paper
Robinson P. et al, (2020), VALUE IN HEALTH, 23, S680 - S680
Frameworks for supporting patient and public involvement in research: Systematic review and co-design pilot
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Greenhalgh T. et al, (2019), Health Expectations, 22, 785 - 801
Making the most of the waiting room: Electronic patient engagement, a mixed methods study.
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Coathup V. et al, (2018), Digit Health, 4
Participant-Centric Initiatives and Medical Research: Scoping Review Protocol.
Journal article
Coathup V. et al, (2017), JMIR Res Protoc, 6
Testing the NHS: the tensions between personalized and collective medicine produced by personal genomics in the UK
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Finlay T., (2017), New Genetics and Society, 36, 227 - 249