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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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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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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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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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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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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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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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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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‘Avoiding harm to others’ considerations in relation to parental measles, mumps and rubella (MMR) vaccination discussions – An analysis of an online chat forum

Social science & medicine (1982), 2008-11, Vol.67 (9), p.1382-1390

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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The significance for decision-making of information that is not exchanged by patients and health professionals during consultations

Social science & medicine (1982), 2006-10, Vol.63 (8), p.2065-2078

2006

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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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Offering informed choice about breast screening

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

2014

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Research funding organisations and consumer involvement

Journal of health services research & policy, 2003-07, Vol.8 (3), p.129

2003

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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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Evidence-informed patient choice. Practical issues of involving patients in decisions about health care technologies

International journal of technology assessment in health care, 1998, Vol.14 (2), p.212

1998

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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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Supporting Consumer Involvement in Decision Making: what Constitutes Quality in Consumer Health Information?

International journal for quality in health care, 1996-10, Vol.8 (5), p.425-437

1996

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Pushing poverty off limits: quality improvement and the architecture of healthcare values

BMC medical ethics, 2021-07, Vol.22 (1), p.1-91, Article 91

2021

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Sharing decisions with patients: is the information good enough?

BMJ (Online), 1999-01, Vol.318 (7179), p.318-322

International edition, 1999

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‘Unilateral’ and ‘bilateral’ practitioner approaches in decision-making about treatment

Social science & medicine (1982), 2005-12, Vol.61 (12), p.2611-2627

2005

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Hybrid funerals: how online attendance facilitates and impedes participation

Mortality (Abingdon, England), 2024-07, Vol.29 (3), p.593-611

2024

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How information about other people's personal experiences can help with healthcare decision-making: A qualitative study

Patient education and counseling, 2011-12, Vol.85 (3), p.e291-e298

2011

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Why does funeral attendance matter? Revisiting 'configurational eulogies' in light of the COVID-19 pandemic in the UK

Mortality (Abingdon, England), 2023-06, Vol.ahead-of-print (ahead-of-print), p.1-22

2023

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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

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

How the stigma of low literacy can impair patient-professional spoken interactions and affect health: insights from a qualitative investigation

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

Vaginal birth after caesarean section: why is uptake so low? Insights from a meta-ethnographic synthesis of women's accounts of their birth choices

Doctors' perspectives on PSA testing illuminate established differences in prostate cancer screening rates between Australia and the UK: a qualitative study

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

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

‘Avoiding harm to others’ considerations in relation to parental measles, mumps and rubella (MMR) vaccination discussions – An analysis of an online chat forum

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

The significance for decision-making of information that is not exchanged by patients and health professionals during consultations

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?

Offering informed choice about breast screening

Research funding organisations and consumer involvement

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

Evidence-informed patient choice. Practical issues of involving patients in decisions about health care technologies

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

Supporting Consumer Involvement in Decision Making: what Constitutes Quality in Consumer Health Information?

Pushing poverty off limits: quality improvement and the architecture of healthcare values

Sharing decisions with patients: is the information good enough?

‘Unilateral’ and ‘bilateral’ practitioner approaches in decision-making about treatment

Hybrid funerals: how online attendance facilitates and impedes participation

How information about other people's personal experiences can help with healthcare decision-making: A qualitative study

Why does funeral attendance matter? Revisiting 'configurational eulogies' in light of the COVID-19 pandemic in the UK

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