Learning
Content: Analysis and Interpretation of Clinical Trials: analysis of continuous outcomes in parallel-arm trials and common myths
Date: 24 September 2021. This event is now closed.
Duration: (live session): 90 minutes
Structure: Pre-recorded material and a live session. Participants will be required to familiarise themselves with the pre-recorded content before attending a live session.
Brief description: The pre-recorded lectures will discuss key topics in clinical trials including trial design, randomisation and non-inferiority trials. Participants will be required to familiarise themselves with the pre-recorded content before attending the live session. The live session will assume an understanding of the basic concepts and definitions and focus on statistical analysis of continuous outcomes from parallel-arm randomised clinical trials (RCTs) and discuss myths around elementary statistical principles in RCTs.
Who should attend: Individuals involved in conducting, planning or analysis of clinical trials or RCTs, students/teachers of epidemiology.
Objective(s): Introduce key concepts in the design of clinical trials, discuss statistical analyses of continuous outcomes in parallel-arm trials and clarify myths surrounding basic statistical principles in RCTs.
Learning outcomes: Participants will be able to describe different trial and randomisation designs, identify the appropriate statistical methods for analysing continuous outcomes and interpret results of RCTs.
Historical and ethical issues in trial design
43 min
An introduction to randomization for clinical trials 1
34 min
An introduction to randomization for clinical trials 2
20 min
Design and conduct of non-inferiority trials
32 min