Design and Interpretation of Clinical Trials

Instructors: Janet Holbrook, PhD, MPH +1 more

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Skills you'll gain

  •   Ethical Standards And Conduct
  •   Medical Science and Research
  •   Statistical Analysis
  •   Statistical Hypothesis Testing
  •   Statistical Methods
  •   Clinical Trials
  •   Scientific Methods
  •   Data Collection
  •   Biostatistics
  •   Regulatory Compliance
  •   Sample Size Determination
  • There are 6 modules in this course

    The course will explain the basic principles for 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. We will also explain some of the mechanics of clinical trials, like randomization and blinding of treatment. In the second half of the course, we will explain how clinical trials are analyzed and interpreted. Finally, we will review the essential ethical consideration involved in conducting experiments on people.

    Randomization and Masking

    Outcomes and Analysis

    Ethics

    Reporting Results

    Randomized Clinical Trials

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