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Rick Chappell

Publications and source records attributed to Rick Chappell.

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BAyesian Bent-Line Regression model for longitudinal data with an application to the study of cognitive performance trajectories in Wisconsin Registry for Alzheimer's Prevention

Preclinical Alzheimer's disease (AD), the earliest stage in the AD continuum, can last fifteen to twenty years, with cognitive decline trajectories nonlinear and heterogeneous between subjects. Characterizing cognitive decline in the preclinical phase of AD is critical for the development of early intervention strategies when disease-modifying therapies may be most effective. In the last decade, there has been an increased interest in the application of change point (CP) models to longitudinal cognitive outcomes. Because patients' change points can vary greatly, it is essential to model this variation. In this paper, we introduce a BAyesian Bent-Line Regression model longitudinal data on cognitive function in middle-aged adults with a high risk of AD. We provide an approach for estimating the fixed (group-level) and random (person-level) CPs, slopes pre- and post-CP, and intercepts at CP for cognition. Our model not only estimates the individual cognitive trajectories but also the distributions of the cognitive bent line curves at each age, enabling researchers and clinicians to estimate subjects' quantiles. Simulation studies show that the estimation and inferential procedures perform reasonably well in finite samples. The practical use is illustrated by an application to a longitudinal cognitive composite in the Wisconsin Registry for Alzheimer's Prevention (WRAP).

stat.ME

Robust Blocked Response-Adaptive Randomization Designs

In most clinical trials, patients are randomized with equal probability among treatments to obtain an unbiased estimate of the treatment effect. Response-adaptive randomization (RAR) has been proposed for ethical reasons, where the randomization ratio is tilted successively to favor the better performing treatment. However, the substantial disagreement regarding bias due to time-trends in adaptive randomization is not fully recognized. The type-I error is inflated in the traditional Bayesian RAR approaches when a time-trend is present. In our approach, patients are assigned in blocks and the randomization ratio is recomputed for blocks rather than traditional adaptive randomization where it is done per patient. We further investigate the design with a range of scenarios for both frequentist and Bayesian designs. We compare our method with equal randomization and with different numbers of blocks including the traditional RAR design where randomization ratio is altered patient by patient basis. The analysis is stratified if there are two or more patients in each block. Small blocks should be avoided due to the possibility of not acquiring any information from the $\mu_i$. On the other hand, RAR with large blocks has a good balance between efficiency and treating more subjects to the better-performing treatment, while retaining blocked RAR's unique unbiasedness.

stat.AP

Imbalanced Randomization in Clinical Trials

Randomization is a common technique used in clinical trials to eliminate potential bias and confounders in a patient population. Equal allocation to treatment groups is the standard due to its optimal efficiency in many cases. However, in certain scenarios, unequal allocation can improve efficiency. In superiority trials with more than two groups, the optimal randomization is not always a balanced randomization. In non-inferiority trials, additive margin with equal variance is the only instance with balanced randomization. Optimal randomization for non-inferiority trials can be far from 1:1 and can greatly improve efficiency, a fact which is commonly overlooked. A tool for sample size calculation for non-inferiority trials with additive or multiplicative margin with normal, binomial or Poisson distribution is available at http://www.statlab.wisc.edu/shiny/SSNI/.

stat.AP