Chapter 12. Study Designs

  1. Chap T. Le Distinguished Professor of Biostatistics Director of Biostatistics

Published Online: 20 MAY 2003

DOI: 10.1002/0471308889.ch12

Introductory Biostatistics

Introductory Biostatistics

How to Cite

Le, C. T. (2003) Study Designs, in Introductory Biostatistics, John Wiley & Sons, Inc., Hoboken, NJ, USA. doi: 10.1002/0471308889.ch12

Author Information

  1. Comprehensive Cancer Center, University of Minnesota, USA

Publication History

  1. Published Online: 20 MAY 2003
  2. Published Print: 21 MAR 2003

ISBN Information

Print ISBN: 9780471418160

Online ISBN: 9780471308881

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Keywords:

  • study design;
  • retrospective study;
  • prospective study;
  • cohort design;
  • retrospective study of past events;
  • clinical trial;
  • phase I;
  • phase II;
  • phase III;
  • designing phase I trials;
  • cohort-escalation trial;
  • maximum-tolerated dose;
  • sample size determination;
  • continuous endpoint;
  • design for selection;
  • toxicity monitoring;
  • proportional hazards model;
  • planning of a clinical trial;
  • sample size for a case-control study;
  • design of a matched case-control study;
  • logistic regression

Summary

In this chapter we focus on study designs. However, since in biomedical research, the sample survey is not a common form of study, and prospective studies of past events and cohort studies are not often conducted, we put more emphasis on the designs of clinical trials which are important because they are experiments on human beings, and of case-control studies, which are the most popular of all study designs. A problem solving section appears at the end of the chapter.