Abstract
We discuss different methods of sample size calculation for two independent means, aiming to provide insight into the calculation of sample size at the design stage of a parallel two-arm randomised controlled trial (RCT). We compare different methods for sample size calculation, using published results from a previous RCT. We use variances and correlation coefficients to compare sample sizes using different methods, including1. The choice of the primary outcome measure: post-intervention score vs. change from baseline score.2. The choice of statistical methods: t-test without using correlation coefficients vs. analysis of covariance (ANCOVA).We show that the required sample size will depend on whether the outcome measure is the post-intervention score, or the change from baseline score, with or without baseline score included as a covariate. We show that certain assumptions have to be met when using simplified sample size equations, and discuss their implications in sample size calculation when planning an RCT. We strongly recommend publishing the crucial result “mean change (SE, standard error)” in a study paper, because it allows (i) the calculation of the variance of the change score in each arm, and (ii) to pool the variances from both arms. It also enables us to calculate the correlation coefficient in each arm. This subsequently allows us to calculate sample size using change score as the outcome measure. We use simulation to demonstrate how sample sizes by different methods are influenced by the strength of the correlation.
Highlights
Sample size calculations for a parallel two-arm trial with a continuous outcome measure can be undertaken based on (i) a pre-specified difference between arms at the post-intervention endpoint and (ii) an estimate of the standard deviation (SD) of the outcome measure
We show that the required sample size will depend on whether the outcome measure is the post-intervention score, or the change from baseline score, with or without baseline score included as a covariate
It is possible to carry out a power calculation based on analysis of covariance (ANCOVA) where the baseline measure is included as a covariate in the analysis
Summary
Sample size calculations for a parallel two-arm trial with a continuous outcome measure can be undertaken based on (i) a pre-specified difference between arms at the post-intervention endpoint and (ii) an estimate of the standard deviation (SD) of the outcome measure. If the outcome variable is measured at baseline, an alternative outcome measure is change from baseline instead of the post-intervention measure. Use of this alternative outcome measure would result in a different power calculation from that obtained using the post-intervention as the outcome measure. We use results from a published paper for the MOSAIC trial [1] to compare different methods for sample size calculation. We aim to provide insight into sample size calculations at the design stage of an RCT
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.