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What Is the Value of the Routine Use of Patient-Reported Outcome Measures Toward Improvement of Patient Outcomes, Processes of Care, and Health Service Outcomes in Cancer Care? A Systematic Review of Controlled Trials

Journal of clinical oncology, 2014-05, Vol.32 (14), p.1480-1501

2014

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Symptom Cluster Patterns During the First Year After Diagnosis with Cancer

Journal of pain and symptom management, 2010-05, Vol.39 (5), p.847-858

2010

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Patient-Reported Self-Efficacy, Anxiety, and Health-Related Quality of Life During Chemotherapy: Results From a Longitudinal Study

Oncology nursing forum, 2017-01, Vol.44 (1), p.127

2017

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Sleep and Sleep-Wake Disturbances in Care Recipient-Caregiver Dyads in the Context of a Chronic Illness: A Critical Review of the Literature

Journal of pain and symptom management, 2013-03, Vol.45 (3), p.579-594

2013

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Trajectories and predictors of state and trait anxiety in patients receiving chemotherapy for breast and colorectal cancer: Results from a longitudinal study

European journal of oncology nursing : the official journal of European Oncology Nursing Society, 2016-10, Vol.24, p.1-7

2016

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Self care and end of life care in advanced cancer: Literature review

European Journal of Oncology Nursing, 2009-12, Vol.13 (5), p.386-398

2009

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Understanding factors that impact on health care professionals’ risk perceptions and responses toward Clostridium difficile and meticillin-resistant Staphylococcus aureus : A structured literature review

American journal of infection control, 2013-05, Vol.41 (5), p.394-400

2013

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Understanding factors that impact on public and patient’s risk perceptions and responses toward Clostridium difficile and other health care-associated infections: A structured literature review

American journal of infection control, 2013-06, Vol.41 (6), p.542-548

2013

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Exercise intervention for patients surgically treated for Non-Small Cell Lung Cancer (NSCLC): A systematic review

Surgical oncology, 2014-03, Vol.23 (1), p.17-30

2014

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Self-care and end of life care—patients’ and carers’ experience a qualitative study utilising serial triangulated interviews

Supportive care in cancer, 2012-08, Vol.20 (8), p.1619-1627

2012

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Evaluation of the feasibility and acceptability of an oral care diary by patients during chemotherapy

International journal of nursing studies, 2007-07, Vol.44 (5), p.693-701

2007

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Development of a novel remote patient monitoring system: the advanced symptom management system for radiotherapy to improve the symptom experience of patients with lung cancer receiving radiotherapy

Cancer nursing, 2015-03, Vol.38 (2), p.E37

2015

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Let patients drive the research

Nurse researcher, 2012, Vol.19 (3), p.46

Kearney, Nora

2012

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Benefits of supervised group exercise programme for women being treated for early stage breast cancer: pragmatic randomised controlled trial

BMJ (British Medical Journal), 2007-03, Vol.334 (7592), p.517-520

International edition, 2007

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Correction to: Complementary and alternative medicine use in breast cancer patients in Europe

Supportive care in cancer, 2024-02, Vol.32 (2), p.102-102, Article 102

2024

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An Interpretative Phenomenological Analysis of the lived experience of multiple concurrent symptoms in patients with lung cancer: A contribution to the study of symptom clusters

European journal of oncology nursing : the official journal of European Oncology Nursing Society, 2014-06, Vol.18 (3), p.310-315

2014

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Constructing identities in the media: newspaper coverage analysis of a major UK Clostridium difficile outbreak

Journal of advanced nursing, 2014-07, Vol.70 (7), p.1542-1552

2014

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Engaging patients in health care: An empirical study of the role of engagement on attitudes and action

Patient education and counseling, 2009-01, Vol.74 (1), p.84-90

2009

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The Patient Remote Intervention and Symptom Management System (PRISMS) - a Telehealth- mediated intervention enabling real-time monitoring of chemotherapy side-effects in patients with haematological malignancies: study protocol for a randomised controlled trial

Trials, 2015-10, Vol.16 (1), p.472-472, Article 472

2015

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Alterations and Interdependence in Self-Reported Sleep-Wake Parameters of Patient-Caregiver Dyads During Adjuvant Chemotherapy for Breast Cancer

Oncology nursing forum, 2016-05, Vol.43 (3), p.288

2016

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Patient and public involvement: models and muddles

Journal of clinical nursing, 2009-09, Vol.18 (18), p.2547-2554

2009

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A review of literature about involving people affected by cancer in research, policy and planning and practice

Patient education and counseling, 2007-01, Vol.65 (1), p.21-33

2007

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Corrigendum to “Harnessing the power of information and communication technologies to meet patients’ informational needs” [EJC Supplements, 3 (2005) 479, Abstract 1662]

European journal of cancer (1990), 2006-05, Vol.42 (7), p.988-988

Kearney, Nora

2006

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Disrupted lives and threats to identity: The experiences of people with colorectal cancer within the first year following diagnosis

Health (London, England : 1997), 2010-03, Vol.14 (2), p.131-146

2010

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What Is the Value of the Routine Use of Patient-Reported Outcome Measures Toward Improvement of Patient Outcomes, Processes of Care, and Health Service Outcomes in Cancer Care? A Systematic Review of Controlled Trials

Symptom Cluster Patterns During the First Year After Diagnosis with Cancer

Patient-Reported Self-Efficacy, Anxiety, and Health-Related Quality of Life During Chemotherapy: Results From a Longitudinal Study

Sleep and Sleep-Wake Disturbances in Care Recipient-Caregiver Dyads in the Context of a Chronic Illness: A Critical Review of the Literature

Trajectories and predictors of state and trait anxiety in patients receiving chemotherapy for breast and colorectal cancer: Results from a longitudinal study

Self care and end of life care in advanced cancer: Literature review

Understanding factors that impact on health care professionals’ risk perceptions and responses toward Clostridium difficile and meticillin-resistant Staphylococcus aureus : A structured literature review

Understanding factors that impact on public and patient’s risk perceptions and responses toward Clostridium difficile and other health care-associated infections: A structured literature review

Exercise intervention for patients surgically treated for Non-Small Cell Lung Cancer (NSCLC): A systematic review

Self-care and end of life care—patients’ and carers’ experience a qualitative study utilising serial triangulated interviews

Evaluation of the feasibility and acceptability of an oral care diary by patients during chemotherapy

Development of a novel remote patient monitoring system: the advanced symptom management system for radiotherapy to improve the symptom experience of patients with lung cancer receiving radiotherapy

Let patients drive the research

Benefits of supervised group exercise programme for women being treated for early stage breast cancer: pragmatic randomised controlled trial

Correction to: Complementary and alternative medicine use in breast cancer patients in Europe

An Interpretative Phenomenological Analysis of the lived experience of multiple concurrent symptoms in patients with lung cancer: A contribution to the study of symptom clusters

Constructing identities in the media: newspaper coverage analysis of a major UK Clostridium difficile outbreak

Engaging patients in health care: An empirical study of the role of engagement on attitudes and action

The eSMART study protocol: a randomised controlled trial to evaluate electronic symptom management using the advanced symptom management system (ASyMS) remote technology for patients with cancer

The Patient Remote Intervention and Symptom Management System (PRISMS) - a Telehealth- mediated intervention enabling real-time monitoring of chemotherapy side-effects in patients with haematological malignancies: study protocol for a randomised controlled trial

Alterations and Interdependence in Self-Reported Sleep-Wake Parameters of Patient-Caregiver Dyads During Adjuvant Chemotherapy for Breast Cancer

Patient and public involvement: models and muddles

A review of literature about involving people affected by cancer in research, policy and planning and practice

Corrigendum to “Harnessing the power of information and communication technologies to meet patients’ informational needs” [EJC Supplements, 3 (2005) 479, Abstract 1662]

Disrupted lives and threats to identity: The experiences of people with colorectal cancer within the first year following diagnosis

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