Lista de obras - Penny Wright - Dominio Público Uruguay

A Rasch and factor analysis of the Functional Assessment of Cancer Therapy-General (FACT-G)

artículo científico publicado en 2007

A qualitative metasynthesis exploring the impact of prostate cancer and its management on younger, unpartnered and gay men.

artículo científico publicado en 2017

Beyond lip service and box ticking: how effective patient engagement is integral to the development and delivery of patient-reported outcomes

artículo científico publicado en 2015

Cancer patients' and clinicians' opinions on the best time in secondary care to approach patients for recruitment to longitudinal questionnaire-based research

artículo científico publicado en 2012

Changing Current Practice in Urology: Improving Guideline Development and Implementation Through Stakeholder Engagement

artículo científico publicado en 2017

Computer-assisted questionnaires may facilitate collection of quality-of-life (QOL) data: At a cost

Costs of cancer care for use in economic evaluation: a UK analysis of patient-level routine health system data ⬇️

artículo científico publicado en 2015

Detecting social problems in cancer patients

artículo científico publicado en 2001

Developing a useful, user-friendly website for cancer patient follow-up: users' perspectives on ease of access and usefulness

artículo científico publicado en 2012

Development and evaluation of a specifically designed website for haematopoietic stem cell transplant patients in Leeds

artículo científico

Development and evaluation of an instrument to assess social difficulties in routine oncology practice.

artículo científico publicado en 2005

Development of an Item Pool for a Needs-Based Measure of Quality of Life of Carers of a Family Member with Dementia ⬇️

article

Ethnicity and the prostate cancer experience: a qualitative metasynthesis ⬇️

artículo científico publicado en 2016

Evaluating Patient Reported Outcome Measures (PROMs) for bladder cancer: a systematic review using the COSMIN checklist. ⬇️

artículo científico publicado en 2018

Factor analysis of the Hospital Anxiety and Depression Scale from a large cancer population.

artículo científico publicado en 2002

Feasibility and compliance of automated measurement of quality of life in oncology practice.

artículo científico publicado en 2003

Feasibility test of a UK-scalable electronic system for regular collection of patient-reported outcome measures and linkage with clinical cancer registry data: the electronic Patient-reported Outcomes from Cancer Survivors (ePOCS) system ⬇️

artículo científico publicado en 2011

Health-related quality of life after colorectal cancer in England: a patient-reported outcomes study of individuals 12 to 36 months after diagnosis

artículo científico publicado en 2015

Health-related quality of life in cancer survivorship: Predictive power of the Social Difficulties Inventory ⬇️

artículo científico publicado en 2017

Identifying Social Distress: A Cross-Sectional Survey of Social Outcomes 12 to 36 Months After Colorectal Cancer Diagnosis ⬇️

artículo científico publicado en 2015

Illness perceptions within 6 months of cancer diagnosis are an independent prospective predictor of health-related quality of life 15 months post-diagnosis ⬇️

artículo científico publicado en 2015

Improvements in measuring the health-related quality of life of cancer patients.

artículo científico publicado en 2006

Integrating cancer survivors' experiences into UK cancer registries: design and development of the ePOCS system (electronic Patient-reported Outcomes from Cancer Survivors) ⬇️

artículo científico publicado en 2011

Integrating patient reported outcomes with clinical cancer registry data: a feasibility study of the electronic Patient-Reported Outcomes From Cancer Survivors (ePOCS) system ⬇️

artículo científico publicado en 2013

Life after prostate cancer diagnosis: protocol for a UK-wide patient-reported outcomes study ⬇️

artículo científico publicado en 2016

Managing social difficulties: roles and responsibilities of patients and staff.

artículo científico publicado en 2010

Maximising Recruitment to Randomised Controlled Trials: The Role of Qualitative Research to Inform Recruitment Challenges.

artículo científico publicado en 2017

Measurement and interpretation of social distress using the social difficulties inventory (SDI).

artículo científico publicado en 2008

Measurement invariance of the 16-item social distress scale

artículo científico publicado en 2010

Measuring social difficulties in routine patient-centred assessment: a Rasch analysis of the social difficulties inventory

article

Patients report improvements in continuity of care when quality of life assessments are used routinely in oncology practice: secondary outcomes of a randomised controlled trial ⬇️

artículo científico publicado en 2010

Psychometric evaluation of the revised Illness Perception Questionnaire (IPQ-R) in cancer patients: confirmatory factor analysis and Rasch analysis

artículo científico publicado en 2013

Psychosocial difficulties, deprivation and cancer: three questionnaire studies involving 609 cancer patients ⬇️

artículo científico publicado en 2005

Psychosocial supportive care services for haematopoietic stem cell transplant patients; a service evaluation of three UK transplant centres

artículo científico publicado en 2013

Rasch analysis of the dimensional structure of the Hospital Anxiety and Depression Scale.

artículo científico publicado en 2006

Routine assessment of social difficulties in cancer patients: are we opening Pandora's box?

artículo científico publicado en 2009

Score equivalence of electronic and paper versions of the Social Difficulties Inventory (SDI-21): a randomised crossover trial in cancer patients

artículo científico publicado en 2012

Screening for social difficulties in cancer patients: clinical utility of the Social Difficulties Inventory

artículo científico publicado en 2007

Self-reported quality of life of individual cancer patients: concordance of results with disease course and medical records.

artículo científico publicado en 2001

The Social Difficulties Inventory (SDI): development of subscales and scoring guidance for staff

artículo científico publicado en 2011

The economic burden of cancer in the UK: a study of survivors treated with curative intent ⬇️

artículo científico publicado en 2015

The social difficulties of cancer patients of South Asian Indian and Pakistani origin: a cross-sectional questionnaire and interview study.

artículo científico publicado en 2011

Traditional and Rasch psychometric analyses of the Quality of Life in Adult Cancer Survivors (QLACS) questionnaire in shorter-term cancer survivors 15 months post-diagnosis

artículo científico publicado en 2014

Translation of the Social Difficulties Inventory (SDI-21) into three South Asian languages and preliminary evaluation of SDI-21(Urdu).

artículo científico publicado en 2010

Urinary, bowel and sexual health in older men from Northern Ireland. ⬇️

artículo científico publicado en 2018

Using international web sites as a cancer resource.

artículo científico publicado en 2002

Using the Clinical Research Network for psychosocial cancer research: lessons learned from two observational studies

artículo científico publicado en 2013

Validation of an item bank for detecting and assessing psychological distress in cancer patients

artículo científico publicado en 2009

Lista de obras de Penny Wright

A Rasch and factor analysis of the Functional Assessment of Cancer Therapy-General (FACT-G)

A qualitative metasynthesis exploring the impact of prostate cancer and its management on younger, unpartnered and gay men.

Beyond lip service and box ticking: how effective patient engagement is integral to the development and delivery of patient-reported outcomes

Cancer patients' and clinicians' opinions on the best time in secondary care to approach patients for recruitment to longitudinal questionnaire-based research

Changing Current Practice in Urology: Improving Guideline Development and Implementation Through Stakeholder Engagement

Computer-assisted questionnaires may facilitate collection of quality-of-life (QOL) data: At a cost

Costs of cancer care for use in economic evaluation: a UK analysis of patient-level routine health system data ⬇️

Detecting social problems in cancer patients

Developing a useful, user-friendly website for cancer patient follow-up: users' perspectives on ease of access and usefulness

Development and evaluation of a specifically designed website for haematopoietic stem cell transplant patients in Leeds

Development and evaluation of an instrument to assess social difficulties in routine oncology practice.

Development of an Item Pool for a Needs-Based Measure of Quality of Life of Carers of a Family Member with Dementia ⬇️

Ethnicity and the prostate cancer experience: a qualitative metasynthesis ⬇️

Evaluating Patient Reported Outcome Measures (PROMs) for bladder cancer: a systematic review using the COSMIN checklist. ⬇️

Factor analysis of the Hospital Anxiety and Depression Scale from a large cancer population.

Feasibility and compliance of automated measurement of quality of life in oncology practice.

Feasibility test of a UK-scalable electronic system for regular collection of patient-reported outcome measures and linkage with clinical cancer registry data: the electronic Patient-reported Outcomes from Cancer Survivors (ePOCS) system ⬇️

Health-related quality of life after colorectal cancer in England: a patient-reported outcomes study of individuals 12 to 36 months after diagnosis

Health-related quality of life in cancer survivorship: Predictive power of the Social Difficulties Inventory ⬇️

Identifying Social Distress: A Cross-Sectional Survey of Social Outcomes 12 to 36 Months After Colorectal Cancer Diagnosis ⬇️

Illness perceptions within 6 months of cancer diagnosis are an independent prospective predictor of health-related quality of life 15 months post-diagnosis ⬇️

Improvements in measuring the health-related quality of life of cancer patients.

Integrating cancer survivors' experiences into UK cancer registries: design and development of the ePOCS system (electronic Patient-reported Outcomes from Cancer Survivors) ⬇️

Integrating patient reported outcomes with clinical cancer registry data: a feasibility study of the electronic Patient-Reported Outcomes From Cancer Survivors (ePOCS) system ⬇️

Life after prostate cancer diagnosis: protocol for a UK-wide patient-reported outcomes study ⬇️

Managing social difficulties: roles and responsibilities of patients and staff.

Maximising Recruitment to Randomised Controlled Trials: The Role of Qualitative Research to Inform Recruitment Challenges.

Measurement and interpretation of social distress using the social difficulties inventory (SDI).

Measurement invariance of the 16-item social distress scale

Measuring social difficulties in routine patient-centred assessment: a Rasch analysis of the social difficulties inventory

Patients report improvements in continuity of care when quality of life assessments are used routinely in oncology practice: secondary outcomes of a randomised controlled trial ⬇️

Psychometric evaluation of the revised Illness Perception Questionnaire (IPQ-R) in cancer patients: confirmatory factor analysis and Rasch analysis

Psychosocial difficulties, deprivation and cancer: three questionnaire studies involving 609 cancer patients ⬇️

Psychosocial supportive care services for haematopoietic stem cell transplant patients; a service evaluation of three UK transplant centres

Rasch analysis of the dimensional structure of the Hospital Anxiety and Depression Scale.

Routine assessment of social difficulties in cancer patients: are we opening Pandora's box?

Score equivalence of electronic and paper versions of the Social Difficulties Inventory (SDI-21): a randomised crossover trial in cancer patients

Screening for social difficulties in cancer patients: clinical utility of the Social Difficulties Inventory

Self-reported quality of life of individual cancer patients: concordance of results with disease course and medical records.

The Social Difficulties Inventory (SDI): development of subscales and scoring guidance for staff

The economic burden of cancer in the UK: a study of survivors treated with curative intent ⬇️

The social difficulties of cancer patients of South Asian Indian and Pakistani origin: a cross-sectional questionnaire and interview study.

Traditional and Rasch psychometric analyses of the Quality of Life in Adult Cancer Survivors (QLACS) questionnaire in shorter-term cancer survivors 15 months post-diagnosis

Translation of the Social Difficulties Inventory (SDI-21) into three South Asian languages and preliminary evaluation of SDI-21(Urdu).

Urinary, bowel and sexual health in older men from Northern Ireland. ⬇️

Using international web sites as a cancer resource.

Using the Clinical Research Network for psychosocial cancer research: lessons learned from two observational studies

Validation of an item bank for detecting and assessing psychological distress in cancer patients