Design and Interpretation of Clinical Trials

Clinical trials are structured experiments used to assess new treatments in humans. Randomised designs provide the most reliable evidence by ensuring objective, unbiased evaluation of benefits and risks. This course introduces key concepts in trial design, reporting, analysis, and the ethical foundations of research involving human participants.

THIS IS AN
ERDERA TRAINING

  • Short Description: The course will explain the basic principles for the design of randomized clinical trials and how they should be reported. In the first part of the course, students will be introduced to terminology used in clinical trials and the several common designs used for clinical trials, such as parallel and cross-over designs. The course will also explain some of the mechanics of clinical trials, like randomization and blinding of treatment. In the second half of the course, clinical trials analysis and interpretation will be explained. Finally, the course will provide a review the essential ethical consideration involved in conducting experiments on people.
  • Topics covered: Types of Trial Designs: parallel, crossover, group allocation, factorial, large simple, equivalency, non-inferiority, and adaptive designs.
  • Provider: Johns Hopkins University via Coursera
  • Level: Basic
  • Language: English
  • Cost: Free
  • Venue: Online
  • Duration: 6 weeks; 2-3 h per week
  • Certificate of Completion: Available/ Paid
e-learning

STATUS

open TRAINING

TYPE

e-learning

LENGTH

15 HOURS

LEVEL

basic

CERTIFICATION

yes

COST

free