174 results on '"Moody, Lesley"'
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2. TOward a comPrehensive supportive Care intervention for Older men with metastatic Prostate cancer (TOPCOP3): A pilot randomized controlled trial and process evaluation
3. Efficacy of the Rehabilitation Planning Consult for Survivors of Head and Neck Cancer: A Phase 2 Randomized Controlled Trial
4. The Cost of Patient Education Materials Development: Opportunities to Identify Value and Priorities
5. Impacts of patient and family engagement in hospital planning and improvement: qualitative interviews with patient/family advisors and hospital staff
6. Reinventing the wheel: The incidence and cost implication of duplication of effort in patient education materials development
7. Patient-Reported Symptom Severity Among 22,650 Cancer Outpatients in the Last Six Months of Life
8. Virtual Cancer Care Beyond the COVID-19 Pandemic: Patient and Staff Perspectives and Recommendations
9. Hospital capacity for patient engagement in planning and improving health services: a cross-sectional survey
10. Symptom burden among head and neck cancer patients in the first year after diagnosis: Association with primary treatment modality
11. Patient Priorities Concerning Treatment Decisions for Advanced Neuroendocrine Tumors Identified by Discrete Choice Experiments.
12. Patient Priorities Concerning Treatment Decisions for Advanced Neuroendocrine Tumors Identified by Discrete Choice Experiments
13. Addressing challenges in telephone triage for outpatient oncology care: A data-centred digital routing solution.
14. Development and implementation of a patient reported experience measurement program to transform cancer care.
15. Efficacy of the Rehabilitation Planning Consult for Survivors of Head and Neck Cancer: A Phase 2 Randomized Controlled Trial
16. Patient-reported symptoms after breast cancer diagnosis and treatment: A retrospective cohort study
17. Symptom Burden at the End of Life for Neuroendocrine Tumors: An Analysis of 2579 Prospectively Collected Patient-Reported Outcomes
18. Patient-reported symptoms following mastectomy alone or lumpectomy plus radiation for early stage breast cancer: a cohort study
19. Psychological aspects of additional procedures following breast reconstruction
20. Transitioning to a New Normal in the Post-COVID Era
21. DEVELOPMENT AND INITIAL PSYCHOMETRIC VALIDATION OF A REAL-TIME PATIENT REPORTED EXPERIENCE MEASURE
22. Consensus on how to optimise patient/family engagement in hospital planning and improvement: a Delphi survey
23. Additional file 1 of Impacts of patient and family engagement in hospital planning and improvement: qualitative interviews with patient/family advisors and hospital staff
24. Additional file 2 of Impacts of patient and family engagement in hospital planning and improvement: qualitative interviews with patient/family advisors and hospital staff
25. Organizational capacity for patient and family engagement in hospital planning and improvement: interviews with patient/family advisors, managers and clinicians
26. Additional file 4 of Hospital capacity for patient engagement in planning and improving health services: a cross-sectional survey
27. Additional file 3 of Hospital capacity for patient engagement in planning and improving health services: a cross-sectional survey
28. Additional file 2 of Hospital capacity for patient engagement in planning and improving health services: a cross-sectional survey
29. Additional file 1 of Hospital capacity for patient engagement in planning and improving health services: a cross-sectional survey
30. Implementation and Outcomes of Virtual Care Across a Tertiary Cancer Center During COVID-19
31. Approaches to optimize patient and family engagement in hospital planning and improvement: Qualitative interviews
32. Improving the quality of self-management support in ambulatory cancer care: a mixed-method study of organisational and clinician readiness, barriers and enablers for tailoring of implementation strategies to multisites
33. The Cost of Patient Education Materials Development: Opportunities to Identify Value and Priorities
34. Development of a national position statement on cancer patient navigation in Canada
35. Élaboration d’un énoncé de position national sur la navigation des patients atteints de cancer au Canada
36. Gaps in the Management of Depression Symptoms Following Cancer Diagnosis: A Population-Based Analysis of Prospective Patient-Reported Outcomes
37. Practical innovation: Advanced practice nurses in cancer care
38. Innovation pratique : infirmières en pratique avancée et soins du cancer
39. Stones: Social Capital in Canadian Aboriginal Communities
40. Improving the quality of self-management support in ambulatory cancer care: a mixed-method study of organisational and clinician readiness, barriers and enablers for tailoring of implementation strategies to multisites.
41. Engaging under- and/or never-engaged populations in health services: A systematic review
42. Tailoring implementation for a cancer self-management support intervention for patients starting chemotherapy.
43. Examining patient and visit characteristics associated with the cancer patient experience.
44. A systematic approach for high-quality care in complex malignant hematology.
45. Patterns of Symptoms Burden in Neuroendocrine Tumors: A Population-Based Analysis of Prospective Patient-Reported Outcomes
46. A Decade in Review
47. Engaging Patient and Family Advisors in Health-Care System Planning: Experiences and Recommendations
48. Symptom burden at the end of life for neuroendocrine tumors: A population-based analysis of patient-reported outcomes.
49. Evaluating cancer patient–reported outcome measures: Readability and implications for clinical use
50. DEVELOPMENT AND INITIAL PSYCHOMETRIC VALIDATION OF A REAL-TIME PATIENT REPORTED EXPERIENCE MEASURE.
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