🎤  Elaine Eisenbeisz      |  đź“…  April 18, 2024   |  đź•’  11 AM Eastern Time US


Description:

In this webinar attendees will learn the statistical power analysis and techniques for determining sample size (a priori techniques) calculation. Also attendees will get work examples in the free to use G*Power software. Some code and demonstrations will be provided for powering studies and performing power analysis simulations in R software.

Questions related to the feasibility of a study can be answered by power analysis:
– How large of a sample will I need to collect in order to see a significant effect?
– How many subjects will I need if I test an effect that is a bit larger? a bit smaller?
Answers to questions like these will give you an idea if your study is indeed “do-able.” 

Why You Should Attend: 

The power of your study is the probability that you will find a statistically significant difference or relationship (an “effect”) if that difference or relationship (effect) truly exists in the population.

A study with too small of a sample size is under-powered. This means that even if the effect you are testing for truly exists, you won’t achieve statistical significance. You will waste time by collecting a sample that is too small to properly power a study. Why perform a research if you can’t see significance for your desired effect?

A study with too large of a sample is over-powered. This means that you’ve collected such a large sample that you will see significance even on very small effects. However, the costs of subject recruitment, data collection, and follow-up (if needed) are quite large. Recruiting more subjects than needed unnecessarily inflates the temporal and monetary costs.


Areas Covered in the Session:

  • The usefulness of power analysis
  • Overview of power analysis theory and concepts
  • Effect size
  • Examples of sample size calculations using G*Power software
  • Examples of sample size calculations using simulation


Who Should Attend:

  • Trial Sponsors
  • Physicians
  • Clinical Investigator
  • Clinical Research Associates
  • Clinical Project Managers/Leaders
  • Regulatory Professionals who use statistical concepts/terminology in reporting
  • Medical Writers who need to interpret statistical reports
  • IRB review board members
  • DSMB members

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