Abstract:
:We evaluate properties of sample size re-estimation (SSR) designs similar to the promising zone design considered by Mehta and Pocock (2011). We evaluate these designs under the assumption of a true effect size of 1.1 down to 0.4 of the protocol-specified effect size by six measures: 1. The probability of a sample size increase, 2. The mean proportional increase in sample size given an increase; 3 and 4. The mean true conditional power with and without a sample size increase; 5 and 6. The expected increase in sample size and power due to the SSR procedure. These measures show the probability of a sample size increase and the cost/benefit for given true effect sizes, particularly when the SSR may either be pursuing a small effect size of little clinical importance or be unnecessary when the true effect size is close to the protocol-specified effect size. The results show the clear superiority of conducting the SSR late in the study and the inefficiency of a mid-study SSR. The results indicate that waiting until late in the study for the SSR yields a smaller, better targeted set of studies with a greater increase in overall power than a mid-study SSR.
journal_name
J Biopharm Statjournal_title
Journal of biopharmaceutical statisticsauthors
Gaffney M,Ware JHdoi
10.1080/10543406.2017.1289943subject
Has Abstractpub_date
2017-01-01 00:00:00pages
797-808issue
5eissn
1054-3406issn
1520-5711journal_volume
27pub_type
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journal_title:Journal of biopharmaceutical statistics
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