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Robust Alternatives to ANCOVA for Estimating the Treatment Effect via a Randomized Comparative Study

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  • Fei Jiang
  • Lu Tian
  • Haoda Fu
  • Takahiro Hasegawa
  • L. J. Wei

Abstract

In comparing two treatments via a randomized clinical trial, the analysis of covariance (ANCOVA) technique is often utilized to estimate an overall treatment effect. The ANCOVA is generally perceived as a more efficient procedure than its simple two sample estimation counterpart. Unfortunately, when the ANCOVA model is nonlinear, the resulting estimator is generally not consistent. Recently, various nonparametric alternatives to the ANCOVA, such as the augmentation methods, have been proposed to estimate the treatment effect by adjusting the covariates. However, the properties of these alternatives have not been studied in the presence of treatment allocation imbalance. In this article, we take a different approach to explore how to improve the precision of the naive two-sample estimate even when the observed distributions of baseline covariates between two groups are dissimilar. Specifically, we derive a bias-adjusted estimation procedure constructed from a conditional inference principle via relevant ancillary statistics from the observed covariates. This estimator is shown to be asymptotically equivalent to an augmentation estimator under the unconditional setting. We utilize the data from a clinical trial for evaluating a combination treatment of cardiovascular diseases to illustrate our findings.

Suggested Citation

  • Fei Jiang & Lu Tian & Haoda Fu & Takahiro Hasegawa & L. J. Wei, 2019. "Robust Alternatives to ANCOVA for Estimating the Treatment Effect via a Randomized Comparative Study," Journal of the American Statistical Association, Taylor & Francis Journals, vol. 114(528), pages 1854-1864, October.
  • Handle: RePEc:taf:jnlasa:v:114:y:2019:i:528:p:1854-1864
    DOI: 10.1080/01621459.2018.1527226
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    Cited by:

    1. Massimiliano Russo & Steffen Ventz & Victoria Wang & Lorenzo Trippa, 2023. "Inference in response‐adaptive clinical trials when the enrolled population varies over time," Biometrics, The International Biometric Society, vol. 79(1), pages 381-393, March.
    2. Zhao, Anqi & Ding, Peng, 2021. "Covariate-adjusted Fisher randomization tests for the average treatment effect," Journal of Econometrics, Elsevier, vol. 225(2), pages 278-294.
    3. Xuan Ye & Heng Li, 2023. "A Non-parametric Test Based on Local Pairwise Comparisons of Patients for Single and Composite Endpoints," Statistics in Biosciences, Springer;International Chinese Statistical Association, vol. 15(2), pages 419-429, July.
    4. David Benkeser & Iván Díaz & Alex Luedtke & Jodi Segal & Daniel Scharfstein & Michael Rosenblum, 2021. "Improving precision and power in randomized trials for COVID‐19 treatments using covariate adjustment, for binary, ordinal, and time‐to‐event outcomes," Biometrics, The International Biometric Society, vol. 77(4), pages 1467-1481, December.

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