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Consultants' forum: should post hoc sample size calculations be done?
1Medical Statistics Group, School of Health and Related Research, University of Sheffield, Sheffield, UK. s.j.walters@sheffield.ac.uk
Pharmaceutical Statistics
|April 18, 2008
Summary
Calculating statistical power after data collection is debated. This practice, often tempting after non-significant results, may not be desirable for clinical trial research protocols. It
Area of Science:
- Clinical Trials
- Biostatistics
- Medical Research
Background:
- Pre-study sample size calculations are mandatory for clinical trial protocols.
- Inadequate patient recruitment can lead to underpowered studies.
- Investigators may face non-statistically significant results with limited power.
Purpose of the Study:
- To debate the desirability of post-hoc power calculations.
- To discuss performing power calculations after data collection and analysis.
Main Methods:
- Literature review and critical analysis of statistical practices.
- Exploration of the implications of post-hoc power analysis in clinical research.
Main Results:
- The article presents arguments for and against post-hoc power calculations.
- It highlights the potential for misinterpretation and bias.
Conclusions:
- Post-hoc power calculations after data analysis are generally discouraged.
- Focus should remain on robust pre-study sample size determination and interpretation of results based on the original protocol.
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