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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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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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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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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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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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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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Hurtful comments are harmful comments: respectful communication is not just an optional extra in healthcare

Health expectations : an international journal of public participation in health care and health policy, 2008-12, Vol.11 (4), p.319-320

Entwistle, Vikki A

2008

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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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Enabling consultations: the facilitative significance of relational aspects of interpersonal communication

Health expectations : an international journal of public participation in health care and health policy, 2010-03, Vol.13 (1), p.1-3

Entwistle, Vikki A.

2010

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Involving service users in qualitative analysis: approaches and assessment

Health expectations : an international journal of public participation in health care and health policy, 2010-06, Vol.13 (2), p.111-112

Entwistle, Vikki A

2010

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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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When service users' support obscures problems with care: the need for rigorous research into patients' experiences

Health expectations : an international journal of public participation in health care and health policy, 2009-06, Vol.12 (2), p.117-119

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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"Was that a success or not a success?": a qualitative study of health professionals' perspectives on support for people with long-term conditions

BMC family practice, 2017-03, Vol.18 (1), p.39, Article 39

2017

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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

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

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

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

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

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

Hurtful comments are harmful comments: respectful communication is not just an optional extra in healthcare

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

Enabling consultations: the facilitative significance of relational aspects of interpersonal communication

Involving service users in qualitative analysis: approaches and assessment

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

When service users' support obscures problems with care: the need for rigorous research into patients' experiences

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

"Was that a success or not a success?": a qualitative study of health professionals' perspectives on support for people with long-term conditions

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