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Mapping the impact of patient and public involvement on health and social care research: a systematic review

Health expectations : an international journal of public participation in health care and health policy, 2014-10, Vol.17 (5), p.637-650

2014

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The GRIPP checklist: Strengthening the quality of patient and public involvement reporting in research

International journal of technology assessment in health care, 2011-10, Vol.27 (4), p.391-399

2011

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Examining the levels of psychological support available to patients with haematological cancer in England: a mixed methods study

BMJ open, 2023-02, Vol.13 (2), p.e060106-e060106

2023

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Electronic cigarettes as a smoking cessation aid for patients with cancer: beliefs and behaviours of clinicians in the UK

BMJ open, 2020-11, Vol.10 (11), p.e037637-e037637

2020

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A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities

The patient : patient-centered outcomes research, 2014-12, Vol.7 (4), p.387-395

2014

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The psychosocial experiences of human papillomavirus (HPV) positive oropharyngeal cancer patients following (chemo)radiotherapy: A systematic review and meta‐ethnography

Psycho-oncology (Chichester, England), 2022-12, Vol.31 (12), p.2009-2019

2022

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If They'd Said You Should Only Drink Five Units I'd Have Listened: A Mixed Methods Study of Alcohol Consumption Following a Diagnosis of Breast Cancer

Psycho-oncology (Chichester, England), 2024-08, Vol.33 (8), p.e9305-n/a

2024

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Shouldn't We Know This Already? UK Women's Views About Communicating the Link Between Alcohol Consumption and Risk of Breast Cancer

Health communication, 2024-08, Vol.39 (9), p.1866-1876

2024

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What if something goes wrong? A grounded theory study of parents’ decision-making processes around mode of breech birth at term gestation

Midwifery, 2019-11, Vol.78, p.114-122

2019

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Patient and public engagement in health-related quality of life and patient-reported outcomes research: what is important and why should we care? Findings from the first ISOQOL patient engagement symposium

Quality of life research, 2015-05, Vol.24 (5), p.1069-1076

2015

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Exploring lessons from Covid‐19 for the role of the voluntary sector in integrated care systems

Health & social care in the community, 2022-11, Vol.30 (6), p.e6689-e6698

2022

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Strategies for living well with hormone-responsive advanced prostate cancer—a qualitative exploration

Supportive care in cancer, 2021-03, Vol.29 (3), p.1317-1325

2021

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Development of the ‘ACT now & check-it-out’ intervention to support patient-initiated follow up for Head and Neck cancer patients

Patient education and counseling, 2024-02, Vol.119, p.108033-108033, Article 108033

2024

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Patient and Public Involvement in Patient-Reported Outcome Measures: Evolution Not Revolution

The patient : patient-centered outcomes research, 2012, Vol.5 (2), p.79-87

2012

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Experiences of Support for Sexual Dysfunction in Men With Prostate Cancer: Findings From a U.K.-Wide Mixed Methods Study

Journal of sexual medicine, 2021-03, Vol.18 (3), p.515-525

2021

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‘Very difficult for an ordinary guy’: Factors influencing the quality of treatment decision-making amongst men diagnosed with localised and locally advanced prostate cancer: Findings from a UK-wide mixed methods study

Patient education and counseling, 2019-04, Vol.102 (4), p.797-803

2019

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PET-CT-guided, symptom-based, patient-initiated surveillance versus clinical follow-up in head neck cancer patients (PETNECK2): study protocol for a multicentre feasibility study and non-inferiority, randomised, phase III trial

BMC cancer, 2024-07, Vol.24 (1), p.823-13, Article 823

2024

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The psychological impact of being on a monitoring pathway for localised prostate cancer: A UK‐wide mixed methods study

Psycho-oncology (Chichester, England), 2019-07, Vol.28 (7), p.1567-1575

2019

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Availability and quality assessment of online nutrition information materials for pelvic cancer patients in the UK

European journal of cancer care, 2019-07, Vol.28 (4), p.e13039-n/a

2019

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Exploring the views of patients' and their family about patient‐initiated follow‐up in head and neck cancer: A mixed methods study

European journal of cancer care, 2022-11, Vol.31 (6), p.e13641-n/a

2022

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Development of the HT&Me intervention to support women with breast cancer to adhere to adjuvant endocrine therapy and improve quality of life

Breast (Edinburgh), 2023-08, Vol.70, p.32-40

2023

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The Warwick Patient Experiences Framework: patient-based evidence in clinical guidelines

International journal for quality in health care, 2014-04, Vol.26 (2), p.151-157

2014

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Adjustment strategies amongst black African and black Caribbean men following treatment for prostate cancer: Findings from the Life After Prostate Cancer Diagnosis (LAPCD) study

European journal of cancer care, 2020-01, Vol.29 (1), p.e13183-n/a

2020

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Reaching consensus on reporting patient and public involvement (PPI) in research: methods and lessons learned from the development of reporting guidelines

BMJ open, 2017-10, Vol.7 (10), p.e016948-e016948

2017

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The POPPY Study: Developing a Model of Family-Centred Care for Neonatal Units

Worldviews on evidence-based nursing, 2012-12, Vol.9 (4), p.243-255

2012

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Mapping the impact of patient and public involvement on health and social care research: a systematic review

The GRIPP checklist: Strengthening the quality of patient and public involvement reporting in research

Examining the levels of psychological support available to patients with haematological cancer in England: a mixed methods study

Electronic cigarettes as a smoking cessation aid for patients with cancer: beliefs and behaviours of clinicians in the UK

A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities

The psychosocial experiences of human papillomavirus (HPV) positive oropharyngeal cancer patients following (chemo)radiotherapy: A systematic review and meta‐ethnography

If They'd Said You Should Only Drink Five Units I'd Have Listened: A Mixed Methods Study of Alcohol Consumption Following a Diagnosis of Breast Cancer

Shouldn't We Know This Already? UK Women's Views About Communicating the Link Between Alcohol Consumption and Risk of Breast Cancer

What if something goes wrong? A grounded theory study of parents’ decision-making processes around mode of breech birth at term gestation

Patient and public engagement in health-related quality of life and patient-reported outcomes research: what is important and why should we care? Findings from the first ISOQOL patient engagement symposium

Exploring lessons from Covid‐19 for the role of the voluntary sector in integrated care systems

Strategies for living well with hormone-responsive advanced prostate cancer—a qualitative exploration

Development of the ‘ACT now & check-it-out’ intervention to support patient-initiated follow up for Head and Neck cancer patients

Patient and Public Involvement in Patient-Reported Outcome Measures: Evolution Not Revolution

Experiences of Support for Sexual Dysfunction in Men With Prostate Cancer: Findings From a U.K.-Wide Mixed Methods Study

‘Very difficult for an ordinary guy’: Factors influencing the quality of treatment decision-making amongst men diagnosed with localised and locally advanced prostate cancer: Findings from a UK-wide mixed methods study

PET-CT-guided, symptom-based, patient-initiated surveillance versus clinical follow-up in head neck cancer patients (PETNECK2): study protocol for a multicentre feasibility study and non-inferiority, randomised, phase III trial

The psychological impact of being on a monitoring pathway for localised prostate cancer: A UK‐wide mixed methods study

Availability and quality assessment of online nutrition information materials for pelvic cancer patients in the UK

Exploring the views of patients' and their family about patient‐initiated follow‐up in head and neck cancer: A mixed methods study

Development of the HT&Me intervention to support women with breast cancer to adhere to adjuvant endocrine therapy and improve quality of life

The Warwick Patient Experiences Framework: patient-based evidence in clinical guidelines

Adjustment strategies amongst black African and black Caribbean men following treatment for prostate cancer: Findings from the Life After Prostate Cancer Diagnosis (LAPCD) study

Reaching consensus on reporting patient and public involvement (PPI) in research: methods and lessons learned from the development of reporting guidelines

The POPPY Study: Developing a Model of Family-Centred Care for Neonatal Units

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