Controlled Clinical Trials – Aims and Designs
Controlled clinical trials provide scientifically valid evidence. But, in order to give valid Information, trials and are designed around a set of aims and hypotheses. This module will cover some of the basic designs, special trial management and data collection issues arising from the design, typical types of analysis, and the resulting statistical report.
Unit 1: Study Aims and Hypotheses
Unit 2: Basic Concepts in Design of Clinical Trials
Unit 3: Measurement
Unit 4: Trial Planning, Trial Management, Data Requirements
Unit 5: Randomization, Blinding, Placebos, Control
Unit 6: Measurement and study variables
Unit 7: Issues in Randomization
Unit 8: Statistical Report
Unit 9: A Web-Based Exam
Unit 10: Practical Exercise
- is the process of making something random, by chance. This can be applied in: Selecting a random sample of a population; or allocating units to different conditions with no order. In clinical trials, randomisation refers to the process of assigning a tria
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