Mona

1234567891011121314151617181920212223242526272829303132333435363738394041424344454647484950515253
Across
  1. 2. Assessment of risks and adverse effects
  2. 6. Recruitment and inclusion of participants into a study
  3. 7. Dissemination of research findings in a journal
  4. 9. Ability of an intervention to produce a desired effect
  5. 12. Undesirable medical occurrence during a study
  6. 14. Ability to keep participants in a study
  7. 23. Metric reflecting average journal citation frequency
  8. 24. Reference to a published scientific work
  9. 25. Organization responsible for initiating and funding a trial
  10. 27. Brief summary of a scientific study
  11. 30. Systematic collection of data on patients or studies
  12. 31. Degree to which participants follow prescribed interventions
  13. 34. Official assessment by a regulatory authority
  14. 38. Statistical combination of results from multiple studies
  15. 39. Evaluation of a manuscript by independent experts
  16. 41. Period of observation after treatment or intervention
  17. 44. Result measured in a clinical investigation
  18. 45. Ongoing oversight of study conduct and data quality
  19. 47. Performance of an intervention in real-world settings
  20. 48. Assignment of participants to study groups by chance
  21. 49. Inclusion and exclusion criteria determining participation
  22. 52. Assignment of participants to intervention groups
  23. 53. Ability to obtain consistent results using the same methods
Down
  1. 1. Process of identifying and inviting participants
  2. 3. Examination of collected data to answer research questions
  3. 4. Outcome measure used to evaluate treatment effects
  4. 5. Review of text to identify language errors
  5. 8. Researcher responsible for conducting a clinical study
  6. 10. Application of statistics to biological and medical research
  7. 11. Independent review of study processes and records
  8. 13. Adverse event resulting in significant harm
  9. 15. Committee responsible for protecting study participants
  10. 16. Inactive treatment used as a control
  11. 17. Conversion of text from one language to another
  12. 18. Concealing treatment allocation from participants or investigators
  13. 19. Grouping participants before randomization
  14. 20. Scientific article submitted for publication
  15. 21. Structured collection of study data
  16. 22. Person managing day-to-day trial activities
  17. 26. Distribution of research findings to stakeholders
  18. 28. Formal modification of a study protocol
  19. 29. Openness in reporting methods and results
  20. 32. Revision of text for clarity and accuracy
  21. 33. Structured review of all relevant evidence
  22. 35. Adherence to study procedures or treatment
  23. 36. Process of assessing participant eligibility
  24. 37. Authorization required before a study can begin
  25. 40. Study conducted at several research sites
  26. 42. Voluntary agreement to participate after receiving information
  27. 43. Periodical publishing scientific research
  28. 46. Specialized vocabulary used in a discipline
  29. 50. Participant discontinuation from a study
  30. 51. Detailed plan describing how a study is conducted