about
Electronic patient self-Reporting of Adverse-events: Patient Information and aDvice (eRAPID): a randomised controlled trial in systemic cancer treatmentA simple practical patient-reported clinic satisfaction measure for young adults.Follow-up care for cancer survivors: the views of clinicians.Follow-up care for cancer survivors: views of the younger adult.Asking the right questions to get the right answers: using cognitive interviews to review the acceptability, comprehension and clinical meaningfulness of patient self-report adverse event items in oncology patients.The effect of Liver Transplantation on the quality of life of the recipient's main caregiver - a systematic review.Training clinicians in how to use patient-reported outcome measures in routine clinical practice.Follow-up care after childhood cancer: survivors' expectations and preferences for care.Follow-up care for young adult survivors of cancer: lessons from pediatrics.Reassurance following breast screening recall for female survivors of Hodgkin's lymphoma.Integrated care pathways for cancer survivors - a role for patient-reported outcome measures and health informatics.Ovarian failure following cancer treatment: current management and quality of life.Oncology professionals' views on the use of antidepressants in cancer patients: a qualitative interview study.A mixed methods approach to adapting health-related quality of life measures for use in routine oncology clinical practice.The detection and management of emotional distress in cancer patients: the views of health-care professionals.Comparison of self-reported late effects with medical records among survivors of childhood cancer.Development of an integrated electronic platform for patient self-report and management of adverse events during cancer treatment.Breast Cancer, Sexuality, and Intimacy: Addressing the Unmet Need.Introduction to special section on digital technology and cancer survivorship.Beyond lip service and box ticking: how effective patient engagement is integral to the development and delivery of patient-reported outcomes.Satisfaction with follow-up consultations among younger adults treated for cancer: the role of quality of life and psychological variables.Gender differences in self-reported late effects, quality of life and satisfaction with clinic in survivors of lymphoma.Benefit finding in survivors of childhood cancer and their parents: further empirical support for the Benefit Finding Scale for Children.Need for psychological follow-up among young adult survivors of childhood cancer.Patients reported outcomes in thoracic surgery.Follow-up after childhood cancer: evaluation of a three-level model.eRAPID electronic patient self-Reporting of Adverse-events: Patient Information and aDvice: a pilot study protocol in pelvic radiotherapy.A systematic review of online systems for patients to report and manage the side effects of cancer treatment (Preprint)Comparison of EORTC QLQ-C30 and PRO-CTCAE™ Questionnaires on Six Symptom ItemsA systematic review of online systems for patients to report and manage the side effects of cancer treatment (Preprint)Psychological Aspects of Hereditary and Non-hereditary Ovarian CancerPredictors of clinic satisfaction among adult survivors of childhood cancerHealth promotion for survivors of childhood cancer: a minimal interventionAre quality of life outcomes comparable following stereotactic radiotherapy and minimally invasive surgery for stage I lung cancer patients?Engaging Patients and Clinicians in Online Reporting of Adverse Effects During Chemotherapy for Cancer: The eRAPID System (Electronic Patient Self-Reporting of Adverse Events: Patient Information and aDvice)
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6505927530
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