Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Search results (34)

« Back to Publications

Chronicity rhetoric in health and welfare systems inhibits patient recovery: a qualitative, ethnographic study of fibromyalgia care

Cupit C. et al, (2025), Social Science and Medicine, 382

Mapping the Social Organisation of Neglect in the Case of Fibromyalgia: Using Smith's Sociology for People to Inform a Systems-Focused Literature Review

Cupit C. et al, (2025), Sociology of Health and Illness, 47

The role of patients, caregivers, and communities in Learning Health Systems: a narrative review

Giacomantonio R. et al, (2025), Frontiers in Health Services, 5

PACFiND: Co-Designing Principles To Inform Reconfiguration Of Fibromyalgia Care Across Health Systems

Hollick R. et al, (2025), ARTHRITIS & RHEUMATOLOGY, 77, 2433 - 2434

How 'Significant Others' Support Parents With Decision-Making About Their Child's Cancer Care: Findings From an Integrative Literature Review

Jestico E. et al, (2025), PSYCHO-ONCOLOGY, 34

Overarching Priorities for Health and Care Research in the United Kingdom: A Coproduced Synthesis of James Lind Alliance ‘Top 10s’

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

Husain L. et al, (2024), British Journal of General Practice, 74, e250 - e257

The ecomap: a tool for extending understanding in hermeneutic phenomenological research.

Jestico E. et al, (2023), Nurse Res, 31, 6 - 13

Safety implications of remote assessments for suspected COVID-19: qualitative study in UK primary care

Wieringa S. et al, (2023), BMJ Quality and Safety, 32, 732 - 741

How ‘significant others’ may support parents with decision-making about their child’s cancer care: An integrative literature review

Jestico ECL. et al, (2023), Journal of Clinical Nursing, 32, 1821 - 1840

Co-design and its consequences: developing a shared patient engagement framework in the IMI-PARADIGM project

Gunn CJ. et al, (2023), SCIENCE AND PUBLIC POLICY, 50, 1018 - 1028

Desperately Seeking Intersectionality in Digital Health Disparity Research: Narrative Review to Inform a Richer Theorization of Multiple Disadvantage

Husain L. et al, (2022), Journal of Medical Internet Research, 24

Planning and Evaluating Remote Consultation Services: A New Conceptual Framework Incorporating Complexity and Practical Ethics

Greenhalgh T. et al, (2021), Frontiers in Digital Health, 3

Could expanding the covid-19 case definition improve the UK’s pandemic response?

FINLAY T. et al, (2021), BMJ: British Medical Journal

Public involvement in the governance of population-level biomedical research: Unresolved questions and future directions

Erikainen S. et al, (2021), Journal of Medical Ethics, 47, 522 - 525

Load More