Justifying sample size for a pilot trial is a reporting requirement, but few pilot trials report a clear rationale for their chosen sample size. Unlike full-scale trials, pilot trials should not be designed to test effectiveness, and so, conventional sample size justification approaches do not apply. Rather, pilot trials typically specify a range of primary and secondary feasibility objectives. Often, these objectives relate to estimation of parameters that inform the sample size justification for the full-scale trial, many of which are binary. These binary outcomes are referred to as “feasibility outcomes” and include expected prevalence of the primary trial outcome, primary outcome availability, or recruitment or retention proportions.
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UT Southwestern Med Ctr, Dept Appl Clin Res, Dallas, TX 75390 USAUT Southwestern Med Ctr, Dept Appl Clin Res, Dallas, TX 75390 USA
Wang, Jijia
Cao, Jing
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Southern Methodist Univ, Dept Stat Sci, Dallas, TX USAUT Southwestern Med Ctr, Dept Appl Clin Res, Dallas, TX 75390 USA
Cao, Jing
Zhang, Song
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UT Southwestern Med Ctr, Dept Populat & Data Sci, 5323 Harry Hines Blvd, Dallas, TX 75390 USAUT Southwestern Med Ctr, Dept Appl Clin Res, Dallas, TX 75390 USA
Zhang, Song
Ahn, Chul
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UT Southwestern Med Ctr, Dept Populat & Data Sci, 5323 Harry Hines Blvd, Dallas, TX 75390 USAUT Southwestern Med Ctr, Dept Appl Clin Res, Dallas, TX 75390 USA