Introduction to Basic Statistics for Clinical Research - PowerPoint PPT Presentation

1 / 12
About This Presentation
Title:

Introduction to Basic Statistics for Clinical Research

Description:

Subgroup analysis and other (mis)use of baseline data in clinical trials. ... of treatment effects in subgroups of patients in randomized clinical trials. ... – PowerPoint PPT presentation

Number of Views:3799
Avg rating:3.0/5.0
Slides: 13
Provided by: darrenm
Category:

less

Transcript and Presenter's Notes

Title: Introduction to Basic Statistics for Clinical Research


1
Introduction to Basic Statistics for Clinical
Research
2
Learning the Language
  • Concept of Sampling
  • Variable types
  • Categorical (qualitative nominal)
  • Ordinal
  • Numerical (continuous interval ratio)
  • Independent vs. Correlated Data
  • Parametric vs. Non-parametric

3
Learning the Language
  • Study Design
  • Sampling Strategy
  • Analysis Types
  • Discrete vs. Time-dependent (survival)
  • Logistic vs Linear Regression
  • Model Building
  • Interactions

4
Sample Size
  • The number of subjects required in a study to
    achieve statistical significance, given a
    number of a priori assumptions.

5
Power Considerations The assumptions
  • Control value or rate
  • Effect size
  • dependent on parameter of interest
  • best to have pilot data
  • Significance level (?)
  • 1-tailed or 2-tailed testing
  • Power (1-?)
  • Confounders
  • Non-compliance
  • Cross-overs
  • Drop Ins
  • Drop Outs
  • Lost to follow up

6
Standards for Effect Size
  • Small -0.2
  • Medium - 0.5
  • Large -0.80
  • only rough guidelines- small medium and large are
    subject dependent

7
Adequacy of Sample Size Matters
8
Effect of trial size on results 24 trials of
?-blockade vs. Placebo
9
Ways to Reduce Required Sample Size
  • Higher Event Rate
  • High risk populations
  • Composite Endpoints
  • Larger Effect Size
  • Lower power
  • Larger ?
  • 1-tailed or 2
  • Change analysis type
  • Time dependent

10
Sample size planning
  • How much money do you have?
  • How much time to you have?
  • How many patients of that specific type can you
    expect to reasonably get?
  • What sample size and study design can I afford?

11
The words to use to describe this
  • The study was designed to have gt80 power to
    detect an effect size of gt20 with a 2-tailed
    significance level of 0.05, with a planned sample
    size of 400 participants in each group.

12
Suggested Reading
  • Reference texts
  • Dawson-Saunders B, Trapp RG. Basic and Clinical
    Biostatistics, Appleton and Lange, Norwalk, CT,
    2nd Edition, 1994.
  • Sackett DL. Clinical Epidemiology a basic
    science for clinical medicine. Little Brown,
    Boston, MA, 2nd Edition, 1991.
  • Selected papers
  • Bias
  • Sackett DL. Bias in analytic research. J Chron
    Dis 1979 3251-63
  • Power
  • Moher D, Dulberg CS, Wells GA. Statistical power,
    sample size, and their reporting in randomized
    controlled trials. JAMA 1994 272 122-4.
  • Subgroup anlayses
  • Assmann SF, Pocock SJ, Enos LE, Kasten LE.
    Subgroup analysis and other (mis)use of baseline
    data in clinical trials. Lancet 2000 355
    1064-1069.
  • Yusuf S, Wittes J, Probstfield J, Tyroler HA.
    Analysis and interpretation of treatment effects
    in subgroups of patients in randomized clinical
    trials. JAMA 1991 266 93-98.
Write a Comment
User Comments (0)
About PowerShow.com