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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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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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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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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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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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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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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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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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The information and support needs of patients discharged after a short hospital stay for treatment of low-risk Community Acquired Pneumonia: implications for treatment without admission

BMC pulmonary medicine, 2008-07, Vol.8 (1), p.11-11, Article 11

2008

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Some Unresolved Ethical Challenges in Healthcare Decision-Making: Navigating Family Involvement

Asian bioethics review, 2020-03, Vol.12 (1), p.27-36

2020

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Protocol for stage 2 of the GaP study (genetic testing acceptability for Paget's disease of bone): a questionnaire study to investigate whether relatives of people with Paget's disease would accept genetic testing and preventive treatment if they were available

BMC health services research, 2008-05, Vol.8 (1), p.116-116, Article 116

2008

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Protocol for stage 1 of the GaP study (Genetic testing acceptability for Paget's disease of bone): an interview study about genetic testing and preventive treatment: would relatives of people with Paget's disease want testing and treatment if they were available?

BMC health services research, 2006-06, Vol.6 (1), p.71-71, Article 71

2006

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Expectations, hopes and moral norms

Health expectations : an international journal of public participation in health care and health policy, 2009-12, Vol.12 (4), p.345-346

Entwistle, Vikki A

2009

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A centralised public information resource for randomised trials: a scoping study to explore desirability and feasibility

BMC health services research, 2005-05, Vol.5 (1), p.39-39, Article 39

2005

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Health visitor professional education and post-qualification clinical supervision: how well does it equip practitioners for dealing with ethical tensions associated with promoting the public health agenda to individual clients?

Primary health care research & development, 2013-01, Vol.14 (1), p.90-102

2013

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Offering informed choice about breast screening

Journal of medical screening, 2014-12, Vol.21 (4), p.194-200

2014

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The requirement for prior consent to participate on survey response rates: a population-based survey in Grampian

BMC health services research, 2003-11, Vol.3 (1), p.21-21, Article 21

2003

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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

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

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

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

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

Enhancing citizen engagement in cancer screening through deliberative democracy

Shared decision-making: enhancing the clinical relevance

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

The information and support needs of patients discharged after a short hospital stay for treatment of low-risk Community Acquired Pneumonia: implications for treatment without admission

Some Unresolved Ethical Challenges in Healthcare Decision-Making: Navigating Family Involvement

Protocol for stage 2 of the GaP study (genetic testing acceptability for Paget's disease of bone): a questionnaire study to investigate whether relatives of people with Paget's disease would accept genetic testing and preventive treatment if they were available

Protocol for stage 1 of the GaP study (Genetic testing acceptability for Paget's disease of bone): an interview study about genetic testing and preventive treatment: would relatives of people with Paget's disease want testing and treatment if they were available?

Expectations, hopes and moral norms

Training in communication of oncology clinicians: a position paper based on the third consensus meeting among European experts in 2018

A centralised public information resource for randomised trials: a scoping study to explore desirability and feasibility

Health visitor professional education and post-qualification clinical supervision: how well does it equip practitioners for dealing with ethical tensions associated with promoting the public health agenda to individual clients?

Offering informed choice about breast screening

The requirement for prior consent to participate on survey response rates: a population-based survey in Grampian

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