Evaluation of Patient-Reported Outcome (PRO) Protocol Content and Reporting in UK Cancer Clinical Trials - EPiC

Keyphrases

1. Cancer Clinical Trials 100%
2. Patient-reported Outcomes 100%
3. In Cancer 100%
4. Trial Design 68%
5. Patient-Reported Outcomes Measurement Information System (PROMIS) 62%
6. Clinical Trials 62%
7. International Perspective 50%
8. Outcome Trials 50%
9. Trial Reporting 50%
10. Trial Protocol 21%
11. Trialists 17%
12. Missing Data 13%
13. Structured Interview 13%
14. Recruitment Strategies 12%
15. Ethnic Groups 12%
16. Journal Editors 9%
17. Accompanying Measures 7%
18. Staff Training 7%
19. Global Experts 7%
20. International Best Practice 7%
21. Clinical Interaction 7%
22. Participant Burden 7%
23. Training Research 7%
24. People with Lived Experience 7%
25. Iterative Codes 7%
26. Regulatory Agencies 7%
27. Best Practice Guidelines 7%
28. Trial Outcomes 7%
29. Research Personnel 7%
30. Effective Integration 7%
31. Coding Frame 7%
32. Reticence 7%
33. Non-reporting 7%
34. Low Priority 7%
35. Improved Communication 7%
36. Stakeholder Groups 7%
37. Chief Investigator 7%
38. Sample Attrition 6%
39. Group Recruitment 6%
40. Missing Samples 6%
41. Ethnically Diverse 6%
42. Trial Results 6%
43. Diverse Populations 6%
44. Design Strategy 6%
45. Inclusive Research 6%
46. Trial Recruitment 6%
47. Inclusion Criteria 6%
48. Multi-centered 6%
49. National Institute for Health Research 6%
50. Tolerability 6%
51. Generalisability 6%
52. Ethnic Background 6%
53. Perceived Barriers 6%
54. Global Stakeholders 6%
55. Participant Engagement 6%
56. Research Portfolio 6%
57. Research Waste 5%