Abstract
BackgroundLongitudinal randomized controlled trials (RCTs) often aim to test and measure the effect of treatment between arms at a single time point. A two-sample χ2 test is a common statistical approach when outcome data are binary. However, only complete outcomes are used in the analysis. Missing responses are common in longitudinal RCTs and by only analyzing complete data, power may be reduced and estimates could be biased. Generalized linear mixed models (GLMM) with a random intercept can be used to test and estimate the treatment effect, which may increase power and reduce bias.MethodsWe simulated longitudinal binary RCT data to compare the performance of a complete case χ2 test to a GLMM in terms of power, type I error, relative bias, and coverage under different missing data mechanisms (missing completely at random and missing at random). We considered how the baseline probability of the event, within subject correlation, and dropout rates under various missing mechanisms impacted each performance measure.ResultsWhen outcome data were missing completely at random, both χ2 and GLMM produced unbiased estimates; however, the GLMM returned an absolute power gain up to from 12.0% as compared to the χ2 test. When outcome data were missing at random, the GLMM yielded an absolute power gain up to 42.7% and estimates were unbiased or less biased compared to the χ2 test.ConclusionsInvestigators wishing to test for a treatment effect between treatment arms in longitudinal RCTs with binary outcome data in the presence of missing data should use a GLMM to gain power and produce minimally unbiased estimates instead of a complete case χ2 test.
Highlights
Longitudinal randomized controlled trials (RCTs) often aim to test and measure the effect of treatment between arms at a single time point
The primary aims of this simulation study were to evaluate the impact of missing completely at random (MCAR) and missing at random (MAR) data on the a) power to detect a treatment effect between two treatment arms at the final time point and b) estimated treatment effect between arms obtained from χ2 and Generalized linear mixed models (GLMM) analyses
For data simulated under the alternative hypothesis, summary of performance measures for χ2 and GLMM methods for each prevalence and correlation combination under each missing mechanism and rates of missingness are presented in Tables 1, 2, 3, 4
Summary
Longitudinal randomized controlled trials (RCTs) often aim to test and measure the effect of treatment between arms at a single time point. Missing responses are common in longitudinal RCTs and by only analyzing complete data, power may be reduced and estimates could be biased. Generalized linear mixed models (GLMM) with a random intercept can be used to test and estimate the treatment effect, which may increase power and reduce bias. Complete binary outcomes Association of response and treatment at a single time point in a randomized clinical trial (RCT) with binary outcomes can be analyzed by using a χ2test of association, methods of moments generalized estimating equations (GEE), or likelihood based generalized linear mixed models (GLMM). A recent review found that 95% of RCTs in the top 4 medical journals had reported some amount of missing outcome data [2]. Potential consequences of missing data include decreased precision, lower power, and biased estimates [3], which can lead to improper inferences of between and within arm effects.
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