Nonparametric identification is not enough, but randomized controlled trials are.

Observational studies Pub Date : 2025-04-11 eCollection Date: 2025-01-01 DOI:10.1353/obs.2025.a956837
P M Aronow, James M Robins, Theo Saarinen, Fredrik Sävje, Jasjeet S Sekhon
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引用次数: 0

Abstract

We argue that randomized controlled trials (RCTs) are special even among studies for which a nonparametric unconfoundedness assumption is credible. This claim follows from two results of Robins and Ritov (1997). First, in settings with at least one continuous confounder, there exists no estimator of the average treatment effect that is uniformly consistent unless the propensity score is known or additional assumptions are made on the complexity of the propensity score function. Second, with binary outcomes, knowledge of the propensity score yields a uniformly consistent estimator and finite-sample valid confidence intervals that shrink at a parametric rate, regardless of how complicated the propensity score function might be. We emphasize the latter point, and note that a successfully executed RCT provides knowledge of the propensity score to the researcher. We conclude that statistical estimation and inference tend to be fundamentally more difficult in observational settings than in RCTs, even when all confounders are observed and measured without error.

非参数识别是不够的,但随机对照试验。
我们认为,随机对照试验(rct)是特殊的研究,即使是非参数无混杂假设是可信的。这一说法来自罗宾斯和里托夫(1997)的两个结果。首先,在至少有一个连续混杂因素的设置中,除非已知倾向得分或对倾向得分函数的复杂性做出额外假设,否则不存在均匀一致的平均治疗效果估计量。其次,对于二元结果,倾向得分的知识产生一致的估计量和有限样本有效置信区间,该置信区间以参数速率收缩,无论倾向得分函数可能有多复杂。我们强调后一点,并注意到成功执行的RCT为研究人员提供了倾向得分的知识。我们的结论是,在观察环境中,统计估计和推断往往比在随机对照试验中更困难,即使在所有混杂因素都被准确地观察和测量时也是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.80
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