Information Package / Course Catalogue
| Course Code | : BİS600 |
| Course Type | : Required |
| Couse Group | : Third Cycle (Doctorate Degree) |
| Education Language | : Turkish |
| Work Placement | : N/A |
| Theory | : 3 |
| Prt. | : 0 |
| Credit | : 3 |
| Lab | : 0 |
| ECTS | : 3 |
To provide the learning of basic concepts of the clinical trials
Introduction to clinical trials; Randomisation, blinding and ethical considerations; Study design and analysis; Special topics in clinical trials: cross-over trials, meta-analysis, repeated measures.
| 1. | Analyse data from a clinical trial, using simple statistical methods, and be able to interpret the results. |
| 2. | Discuss the ethical issues involved in conducting clinical trials. |
| 3. | Be able to implement simple randomisation methods. |
| 4. | Calculate the required sample size for a study. |
| 5. | 199/5000 Learning the methods required for the planning of a clinical trial from the stage of planning to the reporting stage, the rules for conducting clinical trials |
| Type of Assessment | Count | Percent |
|---|---|---|
| Attending Lectures | 1 | %5 |
| Assignment | 1 | %5 |
| Midterm Examination | 1 | %20 |
| Final Examination | 1 | %70 |
| Activities | Count | Preparation | Time | Total Work Load (hours) |
|---|---|---|---|---|
| Lecture - Theory | 14 | 0 | 3 | 42 |
| Quiz | 2 | 1 | 1 | 4 |
| Midterm Examination | 1 | 10 | 2 | 12 |
| Final Examination | 1 | 15 | 2 | 17 |
| TOTAL WORKLOAD (hours) | 75 | |||
PÇ-1 | PÇ-2 | PÇ-3 | PÇ-4 | PÇ-5 | PÇ-6 | PÇ-7 | |
OÇ-1 | 5 | 3 | 3 | 2 | 5 | 3 | 4 |
OÇ-2 | 4 | 5 | 5 | 4 | 4 | 4 | 3 |
OÇ-3 | 4 | 3 | 5 | 3 | 3 | 3 | 3 |
OÇ-4 | 4 | 4 | 4 | 5 | 4 | 4 | 4 |
OÇ-5 | |||||||