scholarly journals Optimal sample sizes for group testing in two-stage sampling

2014 ◽  
Vol 25 (01) ◽  
pp. 12-28 ◽  
Author(s):  
Osval Antonio Montesinos-López ◽  
Kent Eskridge ◽  
Abelardo Montesinos-López ◽  
José Crossa
1998 ◽  
pp. 213-232 ◽  
Author(s):  
Toby Berger ◽  
James W. Mandell
Keyword(s):  

2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Bo Yu ◽  
Xiaonan Liang ◽  
Ying Wang ◽  
Yun Liu ◽  
Qiao Chang ◽  
...  

When designing the sample scheme, it is important to determine the sample size. The survey accuracy and cost of survey and sampling method should be considered comprehensively. In this article, we discuss the method of determining the sample size of complex successive sampling with rotation sample for sensitive issue and deduce the formulas for the optimal sample size under two-stage sampling and stratified two-stage sampling by using Cauchy-Schwartz inequality, respectively, so as to minimize the cost for given sampling errors and to minimize the sampling errors for given cost.


2009 ◽  
Vol 29 (6) ◽  
pp. 643-660 ◽  
Author(s):  
Stefano Conti ◽  
Karl Claxton

Bayesian decision theory can be used not only to establish the optimal sample size and its allocation in a single clinical study but also to identify an optimal portfolio of research combining different types of study design. Within a single study, the highest societal payoff to proposed research is achieved when its sample sizes and allocation between available treatment options are chosen to maximize the expected net benefit of sampling (ENBS). Where a number of different types of study informing different parameters in the decision problem could be conducted, the simultaneous estimation of ENBS across all dimensions of the design space is required to identify the optimal sample sizes and allocations within such a research portfolio. This is illustrated through a simple example of a decision model of zanamivir for the treatment of influenza. The possible study designs include: 1) a single trial of all the parameters, 2) a clinical trial providing evidence only on clinical endpoints, 3) an epidemiological study of natural history of disease, and 4) a survey of quality of life. The possible combinations, samples sizes, and allocation between trial arms are evaluated over a range of cost-effectiveness thresholds. The computational challenges are addressed by implementing optimization algorithms to search the ENBS surface more efficiently over such large dimensions.


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