Objectives
After completing this course, students will be able to:
- understand the different statistical methodological aspects in clinical trials
- gain practical knowledge on planning and analyzing different types of clinical trials and variables.
- understand guidelines in clinical trials, e.g. the CONSORT (Consolidated Standards of Reporting Trials) Statement, and its importance in clinical trial reporting.
- design a simple intervention study covering hypothesis formulation, study design, randomization, outcomes and analysis
- Opettaja
Laura Kortesoja