358 results on '"Rutherford, Claudia"'
Search Results
2. The use of patient reported outcome measures in oncology clinical practice across Australia and New Zealand
3. Current practices and standards regarding provision of information to women newly diagnosed with DCIS: A national survey
4. First Phase Development of a Patient-reported Outcome Measure for Midface Oncology
5. Trials with patient-reported outcomes registered on the Australian New Zealand Clinical Trials Registry (ANZCTR)
6. Assessing chemotherapy-induced peripheral neuropathy with patient reported outcome measures: a systematic review of measurement properties and considerations for future use
7. Introduction to the special section "Reducing research waste in (health-related) quality of life research"
8. Improving the patient-reported outcome sections of clinical trial protocols: a mixed methods evaluation of educational workshops
9. Setting International Standards in Analyzing Patient-Reported Outcomes and Quality of Life Endpoints in Cancer Clinical Trials-Innovative Medicines Initiative (SISAQOL-IMI): stakeholder views, objectives, and procedures
10. Impact of immune checkpoint inhibitors and targeted therapy on health-related quality of life of people with stage III and IV melanoma: a mixed-methods systematic review
11. Single-arm studies involving patient-reported outcome data in oncology: a literature review on current practice
12. How consequences of colorectal cancer treatment are managed: a qualitative study of stakeholder experiences about supportive care and current practices
13. Quality of Life in Women with Ovarian Cancer
14. Association of optimism and social support with health‐related quality of life among Australian women cancer survivors – A cohort study
15. Perceived benefits and limitations of using patient-reported outcome measures in clinical practice with individual patients: a systematic review of qualitative studies
16. Implementing core outcomes in kidney disease: report of the Standardized Outcomes in Nephrology (SONG) implementation workshop
17. The use of proxies and proxy-reported measures: a report of the international society for quality of life research (ISOQOL) proxy task force
18. Patient and healthcare provider perceptions on using patient-reported experience measures (PREMs) in routine clinical care: a systematic review of qualitative studies
19. The use of patient reported outcome measures in oncology clinical practice across Australia and New Zealand
20. Registered Reports at “Quality of Life Research”
21. Using feedback tools to enhance the quality and experience of care
22. Experiences and perspectives of colorectal cancer survivors and general practitioners on the delivery of survivorship care in general practice: a mixed methods study
23. Using Implementation Science Frameworks to Guide the Use of Electronic Patient-Reported Outcome Symptom Monitoring in Routine Cancer Care
24. Enabling cross-cultural data pooling in trials: linguistic validation of head and neck cancer measures for Indian patients
25. How is quality of life defined and assessed in published research?
26. Patient-reported outcomes as predictors of survival in patients with bowel cancer : a systematic review
27. Introduction to “Advancing quality-of-life research by deepening our understanding of response shift”
28. Implementing Patient-Reported Outcome Measures into Clinical Practice Across NSW: Mixed Methods Evaluation of the First Year
29. Views of healthcare professionals about the role of active monitoring in the management of ductal carcinoma in situ (DCIS): Qualitative interview study
30. Patient-reported outcomes in non-muscle invasive bladder cancer: a mixed-methods systematic review
31. Co-production of a systematic review on decision coaching: a mixed methods case study within a review.
32. Impact of weight loss interventions on patient-reported outcomes in overweight and obese adults with type 2 diabetes: a systematic review
33. Trials with proxy-reported outcomes registered on the Australian New Zealand Clinical Trials Registry (ANZCTR)
34. Is quality of life a suitable measure of patient decision aid effectiveness? Sub-analysis of a Cochrane systematic review
35. Patient-reported anxiety and depression measures for use in Indian head and neck cancer populations: a psychometric evaluation
36. A systematic review of body image measures for people diagnosed with head and neck cancer (HNC)
37. Health-Related Quality of Life in Cancer
38. Patient-reported outcome measures for life participation in kidney transplantation: A systematic review
39. Health-related quality of life in patients accessing medicinal cannabis in Australia: The QUEST initiative results of a 3-month follow-up observational study
40. NSP-09 Clinical validation of the steroid symptom questionnaire multiple myeloma (SSQ-MM) in a multi-centre study
41. P-476 More efficient delivery of high-cost standard-of-care therapies in relapsed multiple myeloma using real-time feedback of patient-reported outcome measures: the MY-PROMPT-2 trial
42. Corrigendum to ‘Impact of immune checkpoint inhibitors and targeted therapy on health-related quality of life of people with stage III and IV melanoma: a mixed-methods systematic review [European Journal of Cancer 184 (2023) 83–105]
43. PB2698: MORE EFFICIENT DELIVERY OF HIGH-COST STANDARD-OF-CARE THERAPIES IN RELAPSED MULTIPLE MYELOMA USING REAL-TIME FEEDBACK OF PATIENT-REPORTED OUTCOME MEASURES: THE MY-PROMPT-2 TRIAL
44. Women’s views about current and future management of Ductal Carcinoma in Situ (DCIS): A mixed-methods study
45. Trials with patient-reported outcomes registered on the Australian New Zealand Clinical Trials Registry (ANZCTR)
46. Experiences of colorectal cancer survivors in returning to primary coordinated healthcare following treatment
47. Supportive care interventions for managing gastrointestinal symptoms following treatment for colorectal cancer: a systematic review
48. Development of consensus-based considerations for use of adult proxy reporting: an ISOQOL task force initiative
49. Setting International Standards in Analyzing Patient-Reported Outcomes and Quality of Life Endpoints in Cancer Clinical Trials-Innovative Medicines Initiative (SISAQOL-IMI): stakeholder views, objectives, and procedures
50. Single-arm studies involving patient-reported outcome data in oncology: a literature review on current practice
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