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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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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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“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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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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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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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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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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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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Patients' experiences with partial dentures: a qualitative study

Gerodontology, 2005-12, Vol.22 (4), p.187-192

2005

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Rationalising the 'irrational': a think aloud study of discrete choice experiment responses

Health economics, 2009-03, Vol.18 (3), p.321-336

2009

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Barriers and facilitators to smoking cessation in a cancer context: A qualitative study of patient, family and professional views

BMC cancer, 2017-05, Vol.17 (1), p.348-348, Article 348

2017

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What is an adequate sample size? Operationalising data saturation for theory-based interview studies

Psychology & health, 2010-12, Vol.25 (10), p.1229-1245

2010

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Health professionals’ experiences and perspectives on food insecurity and long‐term conditions: A qualitative investigation

Health & social care in the community, 2020-03, Vol.28 (2), p.404-413

2020

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Do Patient Decision Aids Meet Effectiveness Criteria of the International Patient Decision Aid Standards Collaboration? A Systematic Review and Meta-analysis

Medical Decision Making, 2007-09, Vol.27 (5), p.554-574

2007

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Using the theory of planned behaviour to develop targets for interventions to enhance patient communication during pharmacy consultations for non-prescription medicines

The International journal of pharmacy practice, 2014-12, Vol.22 (6), p.386-396

2014

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Who are your public? A survey comparing the views of a population-based sample with those of a community-based public forum in Scotland

Health & social care in the community, 2005-03, Vol.13 (2), p.164-169

2005

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

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

“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

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

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

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?

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?

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

Patients' experiences with partial dentures: a qualitative study

Rationalising the 'irrational': a think aloud study of discrete choice experiment responses

Barriers and facilitators to smoking cessation in a cancer context: A qualitative study of patient, family and professional views

What is an adequate sample size? Operationalising data saturation for theory-based interview studies

Health professionals’ experiences and perspectives on food insecurity and long‐term conditions: A qualitative investigation

Do Patient Decision Aids Meet Effectiveness Criteria of the International Patient Decision Aid Standards Collaboration? A Systematic Review and Meta-analysis

Using the theory of planned behaviour to develop targets for interventions to enhance patient communication during pharmacy consultations for non-prescription medicines

Who are your public? A survey comparing the views of a population-based sample with those of a community-based public forum in Scotland

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