| Literature DB >> 19296774 |
C Hendricks Brown1, Thomas R Ten Have, Booil Jo, Getachew Dagne, Peter A Wyman, Bengt Muthén, Robert D Gibbons.
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.Entities:
Mesh:
Year: 2009 PMID: 19296774 PMCID: PMC2778326 DOI: 10.1146/annurev.publhealth.031308.100223
Source DB: PubMed Journal: Annu Rev Public Health ISSN: 0163-7525 Impact factor: 21.981