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Health in the 'hidden population' of people with low literacy. A systematic review of the literature

BMC public health, 2010-08, Vol.10 (1), p.459-459, Article 459

2010

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Shared decision making: trade-offs between narrower and broader conceptions

Health expectations : an international journal of public participation in health care and health policy, 2011-06, Vol.14 (2), p.210-219

2011

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Reasons for participating in randomised controlled trials: conditional altruism and considerations for self

Trials, 2010-03, Vol.11 (1), p.31-31, Article 31

2010

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General Practitioners' Experiences of, and Responses to, Uncertainty in Prostate Cancer Screening: Insights from a Qualitative Study

PloS one, 2016-04, Vol.11 (4), p.e0153299-e0153299

2016

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Personalised care planning for adults with chronic or long-term health conditions

Cochrane database of systematic reviews, 2015-03, Vol.2015 (3), p.CD010523-CD010523

2015

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Supporting positive experiences and sustained participation in clinical trials: looking beyond information provision

Journal of medical ethics, 2012-12, Vol.38 (12), p.751-756

2012

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Ethical issues raised by thyroid cancer overdiagnosis: A matter for public health?

Bioethics, 2017-10, Vol.31 (8), p.590-598

2017

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Telephone consulting for 'Personalised Care and Support Planning' with people with long-term conditions: a qualitative study of healthcare professionals' experiences during COVID-19 restrictions and beyond

BMC primary care, 2024-05, Vol.25 (1), p.193-15, Article 193

2024

Volltextzugriff (PDF)

Tackling disrespect in health care: The relevance of socio-relational equality

Journal of health services research & policy, 2024-01, Vol.29 (1), p.42-50

2024

Volltextzugriff (PDF)

Implementing and evaluating care and support planning: a qualitative study of health professionals' experiences in public polyclinics in Singapore

BMC primary care, 2023-10, Vol.24 (1), p.212-212, Article 212

2023

Volltextzugriff (PDF)

How the stigma of low literacy can impair patient-professional spoken interactions and affect health: insights from a qualitative investigation

BMC health services research, 2013-08, Vol.13 (1), p.319-319, Article 319

2013

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Why Health and Social Care Support for People with Long-Term Conditions Should be Oriented Towards Enabling Them to Live Well

Health care analysis, 2018-03, Vol.26 (1), p.48-65

2018

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Unifying and universalizing Personalised Care? An analysis of a national curriculum with implications for policy and education relating to person-centred care

Patient education and counseling, 2022-12, Vol.105 (12), p.3422-3428

2022

Volltextzugriff (PDF)

Decision aids for people facing health treatment or screening decisions

Cochrane database of systematic reviews, 2009-01 (3), p.CD001431

2009

Volltextzugriff (PDF)

Addressing Deficits and Injustices: The Potential Epistemic Contributions of Patients to Research

Health care analysis, 2017-12, Vol.25 (4), p.386-403

2017

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Patient involvement in treatment decision-making: The case for a broader conceptual framework

Patient education and counseling, 2006-11, Vol.63 (3), p.268-278

2006

Volltextzugriff (PDF)

Valuing patients' experiences of healthcare processes: Towards broader applications of existing methods

Social science & medicine (1982), 2014-04, Vol.106 (100), p.194-203

2014

Volltextzugriff (PDF)

We need to talk about purpose: a critical interpretive synthesis of health and social care professionals’ approaches to self‐management support for people with long‐term conditions

Health expectations : an international journal of public participation in health care and health policy, 2017-04, Vol.20 (2), p.243-259

2017

Volltextzugriff (PDF)

Empirical relationships between health literacy and treatment decision making: A scoping review of the literature

Patient education and counseling, 2015-03, Vol.98 (3), p.296-309

2015

Volltextzugriff (PDF)

“The more you know, the more you realise it is really challenging to do”: Tensions and uncertainties in person-centred support for people with long-term conditions

Patient education and counseling, 2018-08, Vol.101 (8), p.1460-1467

2018

Volltextzugriff (PDF)

Vaginal birth after caesarean section: why is uptake so low? Insights from a meta-ethnographic synthesis of women's accounts of their birth choices

BMJ open, 2016-01, Vol.6 (1), p.e008881-e008881

2016

Volltextzugriff (PDF)

The value of different aspects of person-centred care: a series of discrete choice experiments in people with long-term conditions

BMJ open, 2017-04, Vol.7 (4), p.e015689-e015689

2017

Volltextzugriff (PDF)

Doctors' perspectives on PSA testing illuminate established differences in prostate cancer screening rates between Australia and the UK: a qualitative study

BMJ open, 2016-12, Vol.6 (12), p.e011932-e011932

2016

Volltextzugriff (PDF)

Risk, Overdiagnosis and Ethical Justifications

Health care analysis, 2019-12, Vol.27 (4), p.231-248

2019

Volltextzugriff (PDF)

Enhancing citizen engagement in cancer screening through deliberative democracy

JNCI : Journal of the National Cancer Institute, 2013-03, Vol.105 (6), p.380-386

2013

Volltextzugriff (PDF)

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Health in the 'hidden population' of people with low literacy. A systematic review of the literature

Shared decision making: trade-offs between narrower and broader conceptions

Reasons for participating in randomised controlled trials: conditional altruism and considerations for self

General Practitioners' Experiences of, and Responses to, Uncertainty in Prostate Cancer Screening: Insights from a Qualitative Study

Personalised care planning for adults with chronic or long-term health conditions

Supporting positive experiences and sustained participation in clinical trials: looking beyond information provision

Ethical issues raised by thyroid cancer overdiagnosis: A matter for public health?

Telephone consulting for 'Personalised Care and Support Planning' with people with long-term conditions: a qualitative study of healthcare professionals' experiences during COVID-19 restrictions and beyond

Tackling disrespect in health care: The relevance of socio-relational equality

Implementing and evaluating care and support planning: a qualitative study of health professionals' experiences in public polyclinics in Singapore

How the stigma of low literacy can impair patient-professional spoken interactions and affect health: insights from a qualitative investigation

Why Health and Social Care Support for People with Long-Term Conditions Should be Oriented Towards Enabling Them to Live Well

Unifying and universalizing Personalised Care? An analysis of a national curriculum with implications for policy and education relating to person-centred care

Decision aids for people facing health treatment or screening decisions

Addressing Deficits and Injustices: The Potential Epistemic Contributions of Patients to Research

Patient involvement in treatment decision-making: The case for a broader conceptual framework

Valuing patients' experiences of healthcare processes: Towards broader applications of existing methods

We need to talk about purpose: a critical interpretive synthesis of health and social care professionals’ approaches to self‐management support for people with long‐term conditions

Empirical relationships between health literacy and treatment decision making: A scoping review of the literature

“The more you know, the more you realise it is really challenging to do”: Tensions and uncertainties in person-centred support for people with long-term conditions

Vaginal birth after caesarean section: why is uptake so low? Insights from a meta-ethnographic synthesis of women's accounts of their birth choices

The value of different aspects of person-centred care: a series of discrete choice experiments in people with long-term conditions

Doctors' perspectives on PSA testing illuminate established differences in prostate cancer screening rates between Australia and the UK: a qualitative study

Risk, Overdiagnosis and Ethical Justifications

Enhancing citizen engagement in cancer screening through deliberative democracy

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