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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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The Routledge Handbook of Feminist Bioethics

1, 2023

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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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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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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

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

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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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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

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

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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

Volltextzugriff (PDF)

Marketing and clinical trials: a case study

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

2007

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Speaking up about safety concerns: multi-setting qualitative study of patients' views and experiences

Quality & safety in health care, 2010-12, Vol.19 (6), p.e33-e33

2010

Volltextzugriff (PDF)

Use of a Birth Plan within Woman-held Maternity Records: A Qualitative Study with Women and Staff in Northeast Scotland

Birth (Berkeley, Calif.), 2014-09, Vol.41 (3), p.283-289

2014

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Advising Patients About Patient Safety: Current Initiatives Risk Shifting Responsibility

Joint Commission journal on quality and patient safety, 2005-09, Vol.31 (9), p.483-494

2005

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Supporting Patient Autonomy: The Importance of Clinician-patient Relationships

The Routledge Handbook of Feminist Bioethics

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

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

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

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

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

Marketing and clinical trials: a case study

Speaking up about safety concerns: multi-setting qualitative study of patients' views and experiences

Use of a Birth Plan within Woman-held Maternity Records: A Qualitative Study with Women and Staff in Northeast Scotland

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

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

Advising Patients About Patient Safety: Current Initiatives Risk Shifting Responsibility

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