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Supporting Patient Autonomy: The Importance of Clinician-patient Relationships

Journal of general internal medicine : JGIM, 2010-07, Vol.25 (7), p.741-745

2010

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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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The Routledge Handbook of Feminist Bioethics

1, 2023

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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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What influences recruitment to randomised controlled trials? A review of trials funded by two UK funding agencies

Trials, 2006-04, Vol.7 (1), p.9-9, Article 9

2006

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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

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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

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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

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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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Decision aids for people facing health treatment or screening decisions

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

2009

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An international core outcome set for evaluating interventions to improve informed consent to clinical trials: The ELICIT Study

Journal of clinical epidemiology, 2021-09, Vol.137, p.14-22

2021

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Understanding and investigating relationality in the capability approach

Journal for the theory of social behaviour, 2022-03, Vol.52 (1), p.86-104

2022

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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

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Addressing complex healthcare problems in diverse settings: Insights from activity theory

Social science & medicine (1982), 2012-02, Vol.74 (3), p.305-312

2012

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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

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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

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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

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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

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Shared decision-making: enhancing the clinical relevance

Journal of the Royal Society of Medicine, 2012-10, Vol.105 (10), p.416-421

2012

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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

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Primary goals, information-giving and men’s understanding: a qualitative study of Australian and UK doctors’ varied communication about PSA screening

BMJ open, 2018-01, Vol.8 (1), p.e018009-e018009

2018

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Marketing and clinical trials: a case study

Trials, 2007-11, Vol.8 (1), p.37-37, Article 37

2007

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Supporting Patient Autonomy: The Importance of Clinician-patient Relationships

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

The Routledge Handbook of Feminist Bioethics

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

What influences recruitment to randomised controlled trials? A review of trials funded by two UK funding agencies

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

Decision aids for people facing health treatment or screening decisions

An international core outcome set for evaluating interventions to improve informed consent to clinical trials: The ELICIT Study

Understanding and investigating relationality in the capability approach

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

Addressing complex healthcare problems in diverse settings: Insights from activity theory

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

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

Shared decision-making: enhancing the clinical relevance

Enhancing citizen engagement in cancer screening through deliberative democracy

Primary goals, information-giving and men’s understanding: a qualitative study of Australian and UK doctors’ varied communication about PSA screening

Marketing and clinical trials: a case study

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