group sequential test
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2020 ◽  
Vol 67 (3) ◽  
pp. 697-705 ◽  
Author(s):  
Michael Alexander Chesnaye ◽  
Steven L. Bell ◽  
James Michael Harte ◽  
David Martin Simpson


Aquaculture ◽  
2020 ◽  
Vol 515 ◽  
pp. 734568
Author(s):  
Zeynep Gökkuş ◽  
Kâmil Alakuş ◽  
Soner Bilen


2019 ◽  
Vol 58 (10) ◽  
pp. 618-627 ◽  
Author(s):  
M. A. Chesnaye ◽  
S. L. Bell ◽  
J. M. Harte ◽  
D. M. Simpson


2018 ◽  
Vol 52 (6) ◽  
pp. 690-695
Author(s):  
Jiacheng Yuan ◽  
Peter Mesenbrink ◽  
Jihao Zhou ◽  
Jeen Liu ◽  
Ray Zhu ◽  
...  


2018 ◽  
Vol 28 (8) ◽  
pp. 2326-2347 ◽  
Author(s):  
Tobias Mütze ◽  
Ekkehard Glimm ◽  
Heinz Schmidli ◽  
Tim Friede

Count data and recurrent events in clinical trials, such as the number of lesions in magnetic resonance imaging in multiple sclerosis, the number of relapses in multiple sclerosis, the number of hospitalizations in heart failure, and the number of exacerbations in asthma or in chronic obstructive pulmonary disease (COPD) are often modeled by negative binomial distributions. In this manuscript, we study planning and analyzing clinical trials with group sequential designs for negative binomial outcomes. We propose a group sequential testing procedure for negative binomial outcomes based on Wald statistics using maximum likelihood estimators. The asymptotic distribution of the proposed group sequential test statistics is derived. The finite sample size properties of the proposed group sequential test for negative binomial outcomes and the methods for planning the respective clinical trials are assessed in a simulation study. The simulation scenarios are motivated by clinical trials in chronic heart failure and relapsing multiple sclerosis, which cover a wide range of practically relevant settings. Our research assures that the asymptotic normal theory of group sequential designs can be applied to negative binomial outcomes when the hypotheses are tested using Wald statistics and maximum likelihood estimators. We also propose two methods, one based on Student’s t-distribution and one based on resampling, to improve type I error rate control in small samples. The statistical methods studied in this manuscript are implemented in the R package gscounts, which is available for download on the Comprehensive R Archive Network (CRAN).



Biometrics ◽  
2018 ◽  
Vol 74 (3) ◽  
pp. 1006-1013 ◽  
Author(s):  
Michael J. Martens ◽  
Brent R. Logan






2014 ◽  
Vol 43 (5) ◽  
pp. 1-1
Author(s):  
Sevil Bacanlı ◽  
Duygu Icen ◽  
Salih Emri


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