General biostatistical quality of study proposals
Item 6: Do you in general have the impression that the biostatistical quality of ethical proposals for studies regulated by AMG/MPG differs compared with proposals in a non-regulated setting? | n=47 (%) |
Yes, ethical proposals for studies regulated by AMG/MPG have a higher biostatistical quality on average | 45 (91.8) |
Yes, ethical proposals for studies in a non-regulated setting have a higher biostatistical quality on average | 0 (0.0) |
No, the biostatistical quality does not differ on average | 2 (4.1) |
Item 11: How do you consider the need for additional training in the following biostatistical areas for investigators submitting protocols to medical ethics committees? | n=45 (%) |
Study design | |
Low | 7 (15.6) |
Middle | 23 (51.1) |
High | 15 (33.3) |
Wording of the study aims, hypotheses and/or endpoints | |
Low | 1 (2.2) |
Middle | 22 (48.9) |
High | 22 (48.9) |
Sample size calculation | |
Low | 2 (4.4) |
Middle | 15 (33.3) |
High | 27 (60.00) |
Not assessable | 1 (2.2) |
Differentiation between confirmatory and exploratory analyses | |
Low | 4 (8.9) |
Middle | 17 (37.8) |
High | 24 (53.3) |
Handling of missing values | |
Low | 2 (4.4) |
Middle | 9 (20.00) |
High | 34 (75.6) |
Description of the statistical analysis | |
Low | 1 (2.3) |
Middle | 23 (52.3) |
High | 20 (45.5) |
Multiple comparisons problems | |
Low | 3 (6.7) |
Middle | 16 (35.6) |
High | 26 (57.8) |
Adjustment for covariables | |
Low | 3 (6.7) |
Middle | 18 (40.0) |
High | 24 (53.3) |
Randomisation/stratification | |
Low | 10 (22.2) |
Middle | 27 (60.00) |
High | 6 (13.3) |
Not assessable | 2 (4.4) |
Additional aspects (added as free-text response by the participants) | |
Data management | |
Regulatory view | |
Testing versus estimating |
AMG/MPG, German Medicines Act/German Act on Medical Devices.