about
Ethnicity and the prostate cancer experience: a qualitative metasynthesisIntegrating patient reported outcomes with clinical cancer registry data: a feasibility study of the electronic Patient-Reported Outcomes From Cancer Survivors (ePOCS) system.Costs of cancer care for use in economic evaluation: a UK analysis of patient-level routine health system data.Validation of an item bank for detecting and assessing psychological distress in cancer patients.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) systemIntegrating cancer survivors' experiences into UK cancer registries: design and development of the ePOCS system (electronic Patient-reported Outcomes from Cancer Survivors)A Rasch and factor analysis of the Functional Assessment of Cancer Therapy-General (FACT-G)Screening for social difficulties in cancer patients: clinical utility of the Social Difficulties InventoryPsychosocial difficulties, deprivation and cancer: three questionnaire studies involving 609 cancer patientsLife after prostate cancer diagnosis: protocol for a UK-wide patient-reported outcomes study.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.A qualitative metasynthesis exploring the impact of prostate cancer and its management on younger, unpartnered and gay men.Illness perceptions within 6 months of cancer diagnosis are an independent prospective predictor of health-related quality of life 15 months post-diagnosis.Cancer patients' and clinicians' opinions on the best time in secondary care to approach patients for recruitment to longitudinal questionnaire-based research.Identifying Social Distress: A Cross-Sectional Survey of Social Outcomes 12 to 36 Months After Colorectal Cancer Diagnosis.The economic burden of cancer in the UK: a study of survivors treated with curative intent.The Social Difficulties Inventory (SDI): development of subscales and scoring guidance for staff.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.Measurement invariance of the 16-item social distress scale.Psychometric evaluation of the revised Illness Perception Questionnaire (IPQ-R) in cancer patients: confirmatory factor analysis and Rasch analysis.Routine assessment of social difficulties in cancer patients: are we opening Pandora's box?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.Score equivalence of electronic and paper versions of the Social Difficulties Inventory (SDI-21): a randomised crossover trial in cancer patients.Using the Clinical Research Network for psychosocial cancer research: lessons learned from two observational studies.Translation of the Social Difficulties Inventory (SDI-21) into three South Asian languages and preliminary evaluation of SDI-21(Urdu).Changing Current Practice in Urology: Improving Guideline Development and Implementation Through Stakeholder Engagement.Health-related quality of life in cancer survivorship: Predictive power of the Social Difficulties Inventory.Beyond lip service and box ticking: how effective patient engagement is integral to the development and delivery of patient-reported outcomes.Health-related quality of life after colorectal cancer in England: a patient-reported outcomes study of individuals 12 to 36 months after diagnosis.Psychosocial supportive care services for haematopoietic stem cell transplant patients; a service evaluation of three UK transplant centres.Detecting social problems in cancer patients.Managing social difficulties: roles and responsibilities of patients and staff.Evaluating Patient Reported Outcome Measures (PROMs) for bladder cancer: a systematic review using the COSMIN checklist.Urinary, bowel and sexual health in older men from Northern Ireland.Maximising Recruitment to Randomised Controlled Trials: The Role of Qualitative Research to Inform Recruitment Challenges.The social difficulties of cancer patients of South Asian Indian and Pakistani origin: a cross-sectional questionnaire and interview study.Measurement and interpretation of social distress using the social difficulties inventory (SDI).Improvements in measuring the health-related quality of life of cancer patients.Rasch analysis of the dimensional structure of the Hospital Anxiety and Depression Scale.
P50
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P50
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