articleTrialsJul 3, 2014GOLD OA

Sample size requirements to estimate key design parameters from external pilot randomised controlled trials: a simulation study

University of Sheffield

PubMed
Indexed incrossrefdoajpubmed

Abstract

Background

External pilot or feasibility studies can be used to estimate key unknown parameters to inform the design of the definitive randomised controlled trial (RCT). However, there is little consensus on how large pilot studies need to be, and some suggest inflating estimates to adjust for the lack of precision when planning the definitive RCT.

Methods

We use a simulation approach to illustrate the sampling distribution of the standard deviation for continuous outcomes and the event rate for binary outcomes. We present the impact of increasing the pilot sample size on the precision and bias of these estimates, and predicted power under three realistic scenarios. We also illustrate the consequences of using a confidence interval argument to inflate estimates so the required power is achieved with a pre-specified level of confidence. We limit our attention to external pilot and feasibility studies prior to a two-parallel-balanced-group superiority RCT.

Citation impact

817
total citations
FWCI
14.78
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100%
References
31
Citations per year

Authors

6

Topics & keywords

Keywords
  • Sample size determination
  • Confidence interval
  • Statistics
  • Standard deviation
  • Randomized controlled trial
  • Medicine
  • Research design
  • Statistical power
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Funding