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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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Development of an e-health app to support women prescribed adjuvant endocrine therapy after treatment for breast cancer

Patient preference and adherence, 2018-01, Vol.12, p.2639-2647

2018

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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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Lifestage differences in young UK women’s reasons for research participation

Health promotion international, 2021-03, Vol.36 (1), p.132-142

2021

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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.1-13, Article 823

2024

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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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Visualizing community networks to recruit South Asian participants for interviews about bowel cancer screening

Journal of cancer policy, 2022-06, Vol.32, p.100333-100333, Article 100333

2022

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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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Adjuvant endocrine therapy after breast cancer: a qualitative study of factors associated with adherence

Patient preference and adherence, 2018-01, Vol.12, p.291-300

2018

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Systematic review of patients’ and healthcare professionals’ views on patient‐initiated follow‐up in treated cancer patients

Cancer medicine (Malden, MA), 2023-08, Vol.12 (15), p.16531-16547

2023

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Comparison of how well conscious cats tolerate blood pressure measurement from the radial and coccygeal arteries

Journal of feline medicine and surgery, 2012-12, Vol.14 (12), p.906-909

2012

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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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Women who are recalled for further investigation for breast screening: psychological consequences 3 years after recall and factors affecting re‐attendance

Journal of public health (Oxford, England), 2001-12, Vol.23 (4), p.292-300

2001

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Developing the evidence base of patient and public involvement in health and social care research: the case for measuring impact

International journal of consumer studies, 2011-11, Vol.35 (6), p.628-632

2011

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Exploring the lived experience of having a hip fracture: identifying patients' perspectives on their health care needs

Brett, Jo

2014

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Patient and Public Involvement in Patient-Reported Outcome Measures

The patient : patient-centered outcomes research, 2012-06, Vol.5 (2), p.79

2012

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"It's a maybe test": men's experiences of prostate specific antigen testing in primary care

British journal of general practice, 2007-04, Vol.57 (537), p.303-310

2007

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PSA testing for prostate cancer: an online survey of the views and reported practice of General Practitioners in the UK

BMC family practice, 2005-06, Vol.6 (1), p.24

2005

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Development and validation of the EBS: a measure to assess women's experience at all stages of the breast screening process

Journal of public health (Oxford, England), 2004-03, Vol.26 (1), p.79-83

2004

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Breast Screening: Adverse Psychological Consequences One Month after Placing Women on Early Recall Because of a Diagnostic Uncertainty. A Multicentre Study

Journal of medical screening, 1997, Vol.4 (3), p.158-168

1997

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Do women who undergo further investigation for breast screening suffer adverse psychological consequences? A multi-centre follow-up study comparing different breast screening result groups five months after their last breast screening appointment

Journal of public health medicine, 1998-12, Vol.20 (4), p.396-403

1998

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

Development of an e-health app to support women prescribed adjuvant endocrine therapy after treatment for breast cancer

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

Lifestage differences in young UK women’s reasons for research participation

Correction: 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

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

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

Visualizing community networks to recruit South Asian participants for interviews about bowel cancer screening

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

Adjuvant endocrine therapy after breast cancer: a qualitative study of factors associated with adherence

Systematic review of patients’ and healthcare professionals’ views on patient‐initiated follow‐up in treated cancer patients

Comparison of how well conscious cats tolerate blood pressure measurement from the radial and coccygeal arteries

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

Women who are recalled for further investigation for breast screening: psychological consequences 3 years after recall and factors affecting re‐attendance

Developing the evidence base of patient and public involvement in health and social care research: the case for measuring impact

Exploring the lived experience of having a hip fracture: identifying patients' perspectives on their health care needs

Patient and Public Involvement in Patient-Reported Outcome Measures

"It's a maybe test": men's experiences of prostate specific antigen testing in primary care

PSA testing for prostate cancer: an online survey of the views and reported practice of General Practitioners in the UK

Development and validation of the EBS: a measure to assess women's experience at all stages of the breast screening process

Breast Screening: Adverse Psychological Consequences One Month after Placing Women on Early Recall Because of a Diagnostic Uncertainty. A Multicentre Study

Do women who undergo further investigation for breast screening suffer adverse psychological consequences? A multi-centre follow-up study comparing different breast screening result groups five months after their last breast screening appointment

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