710 results on '"Snyder, Claire"'
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2. Recommendations to address respondent burden associated with patient-reported outcome assessment
3. A framework for implementing patient-reported outcomes in clinical care: the PROTEUS-practice guide
4. Comparing the Effectiveness of Electronic Symptom Monitoring versus Usual Care in Improving Survival among Patients with Metastatic Cancer -- The PRO-TECT Trial
5. EORTC QLQ-C30 general population normative data for the United States
6. Factors associated with weight gain in pre- and post-menopausal women receiving adjuvant endocrine therapy for breast cancer
7. Factors associated with worsening sexual function during adjuvant endocrine therapy in a prospective clinic-based cohort of women with early-stage breast cancer
8. Knowledge translation concerns for the CONSORT-PRO extension reporting guidance: a review of reviews
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. Data Visualization Strategies to Communicate PRO Data to Patients and Clinicians
11. A PRO-cision medicine intervention to personalize cancer care using patient-reported outcomes: intervention development and feasibility-testing
12. Implementing survivorship care planning in two contrasting health systems: lessons learned from a randomized controlled trial
13. The impact of weight loss on physical function and symptoms in overweight or obese breast cancer survivors: results from POWER-remote
14. In proportion: approaches for displaying patient-reported outcome research study results as percentages responding to treatment
15. Late effects in a high-risk population of breast cancer survivors
16. Association of treatment-emergent symptoms identified by patient-reported outcomes with adjuvant endocrine therapy discontinuation
17. Continuity and coordination of care for childhood cancer survivors with multiple chronic conditions: Results from the Childhood Cancer Survivor Study.
18. Health-care organization characteristics in cancer care delivery: an integrated conceptual framework with content validation
19. Patient-Reported Outcome Measures and Dosimetric Correlates for Early Detection of Acute Radiation Therapy–Related Esophagitis
20. Long‐term outcomes among survivors of childhood osteosarcoma: A report from the Childhood Cancer Survivor Study (CCSS).
21. International guidance on the selection of patient-reported outcome measures in clinical trials: a review
22. Primary Care Utilization and Cardiovascular Screening in Adult Survivors of Childhood Cancer
23. Feasibility of Symptom Monitoring During the First Year of Endocrine Therapy for Early Breast Cancer Using Patient-Reported Outcomes Collected via Smartphone App
24. Making a picture worth a thousand numbers : recommendations for graphically displaying patient-reported outcomes data
25. Comparing Three Ways to Help Cancer Survivors Plan for Follow-Up Care
26. Selecting Patient-Reported Outcome Measures to Contribute to Primary Care Performance Measurement: a Mixed Methods Approach
27. Breast cancer survivorship care plans: what are they covering and how well do they align with national guidelines?
28. Models of Care That Include Primary Care for Adult Survivors of Childhood Cancer: A Realist Review
29. Presenting comparative study PRO results to clinicians and researchers: beyond the eye of the beholder
30. Survivorship care visits in a high-risk population of breast cancer survivors
31. Oh, the Places We’ll Go: Patient-Reported Outcomes and Electronic Health Records
32. 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
33. The Outcomes of Cancer Outcomes Research Focusing on the National Cancer Institute's Quality-of-Care Initiative
34. Feasibility and perception of a question prompt list in outpatient cancer care
35. Data from The Effects of a Remote-based Weight Loss Program on Adipocytokines, Metabolic Markers, and Telomere Length in Breast Cancer Survivors: the POWER-Remote Trial
36. Supplemental Figure 2 from The Effects of a Remote-based Weight Loss Program on Adipocytokines, Metabolic Markers, and Telomere Length in Breast Cancer Survivors: the POWER-Remote Trial
37. Supplemental Legend from The Effects of a Remote-based Weight Loss Program on Adipocytokines, Metabolic Markers, and Telomere Length in Breast Cancer Survivors: the POWER-Remote Trial
38. Supplemental Table 1 from The Effects of a Remote-based Weight Loss Program on Adipocytokines, Metabolic Markers, and Telomere Length in Breast Cancer Survivors: the POWER-Remote Trial
39. Supplemental Figure 1 from The Effects of a Remote-based Weight Loss Program on Adipocytokines, Metabolic Markers, and Telomere Length in Breast Cancer Survivors: the POWER-Remote Trial
40. Presenting comparative study PRO results to clinicians and researchers: beyond the eye of the beholder
41. Graphical displays of patient-reported outcomes (PRO) for use in clinical practice: What makes a pro picture worth a thousand words?
42. International Society for Quality of Life Research commentary on the draft European Medicines Agency reflection paper on the use of patient-reported outcome (PRO) measures in oncology studies
43. Communicating patient-reported outcome scores using graphic formats: results from a mixed-methods evaluation
44. EORTC QLQ-C30 and the Supportive Care Needs Survey
45. Evaluating potential overuse of surveillance care in cancer survivors
46. Prospective assessment of patient-reported outcomes and estradiol and drug concentrations in patients experiencing toxicity from adjuvant aromatase inhibitors
47. Identifying changes in scores on the EORTC-QLQ-C30 representing a change in patients' supportive care needs
48. Cancer patients' function, symptoms and supportive care needs: a latent class analysis across cultures
49. How does pain experience relate to the need for pain relief? A secondary exploratory analysis in a large sample of cancer patients
50. Engaging stakeholders to improve presentation of patient-reported outcomes data in clinical practice
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