Adaptive Designs for Randomized Trials in Public Health

Author:

Brown C. Hendricks1,Ten Have Thomas R.2,Jo Booil3,Dagne Getachew1,Wyman Peter A.4,Muthén Bengt5,Gibbons Robert D.6

Affiliation:

1. Prevention Science and Methodology Group, Department of Epidemiology and Biostatistics, University of South Florida, Tampa, Florida, 33612;

2. Department of Biostatistics, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, 19104

3. Department of Psychiatry and Behavioral Science, Stanford University School of Medicine, Stanford, California, 94305-5795

4. Department of Psychiatry, University of Rochester, Rochester, New York, 14642

5. Graduate School of Education and Information Studies, University of California, Los Angeles, California, 90095-1521

6. Center for Health Statistics, University of Illinois, Chicago, Illinois 60612

Abstract

In this article, we present a discussion of two general ways in which the traditional randomized trial can be modified or adapted in response to the data being collected. We use the term adaptive design to refer to a trial in which characteristics of the study itself, such as the proportion assigned to active intervention versus control, change during the trial in response to data being collected. The term adaptive sequence of trials refers to a decision-making process that fundamentally informs the conceptualization and conduct of each new trial with the results of previous trials. Our discussion below investigates the utility of these two types of adaptations for public health evaluations. Examples are provided to illustrate how adaptation can be used in practice. From these case studies, we discuss whether such evaluations can or should be analyzed as if they were formal randomized trials, and we discuss practical as well as ethical issues arising in the conduct of these new-generation trials.

Publisher

Annual Reviews

Subject

Public Health, Environmental and Occupational Health,General Medicine

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