Sample size requirements to estimate key design parameters from external pilot randomised controlled trials: a simulation study
Abstract
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.
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
- FWCI
- 14.78
- Percentile
- 100%
- References
- 31
Authors
6Topics & keywords
- Sample size determination
- Confidence interval
- Statistics
- Standard deviation
- Randomized controlled trial
- Medicine
- Research design
- Statistical power