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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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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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“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

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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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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

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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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How personal experiences feature in women’s accounts of use of information for decisions about antenatal diagnostic testing for foetal abnormality

Social science & medicine (1982), 2011-03, Vol.72 (5), p.755-762

2011

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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 mutual helping? Examining variable needs for facilitated peer support

Patient education and counseling, 2011-11, Vol.85 (2), p.e120-e125

2011

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Provision of cancer information as a “support for navigating the knowledge landscape”: Findings from a critical interpretive literature synthesis

European journal of oncology nursing : the official journal of European Oncology Nursing Society, 2013-06, Vol.17 (3), p.360-369

2013

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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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Assessing patients’ participation and quality of decision-making: insights from a study of routine practice in diverse settings

Patient education and counseling, 2004-10, Vol.55 (1), p.105-113

2004

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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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Decisions about treatment: interpretations of two measures of control by women having a hysterectomy

Social science & medicine (1982), 2001-09, Vol.53 (6), p.721-732

2001

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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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Methods of hysterectomy: should women have a say?

BMJ (Online), 2005-08, Vol.331 (7512), p.351

2005

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The case of Norplant as an example of media coverage over the life of a new health technology

The Lancet (British edition), 2000-05, Vol.355 (9215), p.1633-1636

2000

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Media coverage of the Child B case

BMJ (Online), 1996-06, Vol.312 (7046), p.1587

International edition, 1996

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Developing information materials to present the findings of technology assessments to consumers. The experience of the NHS Centre for Reviews and Dissemination

International journal of technology assessment in health care, 1998, Vol.14 (1), p.47

1998

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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

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

“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

Enhancing citizen engagement in cancer screening through deliberative democracy

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

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

How personal experiences feature in women’s accounts of use of information for decisions about antenatal diagnostic testing for foetal abnormality

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 mutual helping? Examining variable needs for facilitated peer support

Provision of cancer information as a “support for navigating the knowledge landscape”: Findings from a critical interpretive literature synthesis

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?

Assessing patients’ participation and quality of decision-making: insights from a study of routine practice in diverse settings

Offering informed choice about breast screening

Decisions about treatment: interpretations of two measures of control by women having a hysterectomy

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

Methods of hysterectomy: should women have a say?

The case of Norplant as an example of media coverage over the life of a new health technology

Media coverage of the Child B case

Developing information materials to present the findings of technology assessments to consumers. The experience of the NHS Centre for Reviews and Dissemination

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