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Nonparametric identification is not enough, but randomized controlled trials are

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arxiv 2108.11342 v2 pith:KKQ5UYYR submitted 2021-08-25 stat.ME

classification stat.ME
keywords rctspropensityscoreaverageconsistentcontrolledcovariateestimator
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We argue that randomized controlled trials (RCTs) are special even among settings where average treatment effects are identified by a nonparametric unconfoundedness assumption. This claim follows from two results of Robins and Ritov (1997): (1) with at least one continuous covariate control, no estimator of the average treatment effect exists which is uniformly consistent without further assumptions, (2) knowledge of the propensity score yields a uniformly consistent estimator and honest confidence intervals that shrink at parametric rates with increasing sample size, regardless of how complicated the propensity score function is. We emphasize the latter point, and note that successfully-conducted RCTs provide knowledge of the propensity score to the researcher. We discuss modern developments in covariate adjustment for RCTs, noting that statistical models and machine learning methods can be used to improve efficiency while preserving finite sample unbiasedness. We conclude that statistical inference has the potential to be fundamentally more difficult in observational settings than it is in RCTs, even when all confounders are measured.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. Two Layers of Instability in Causal Estimation

    stat.ML 2026-06 unverdicted novelty 6.5 of 10

    Standard causal estimators like IPW and regression can jump discontinuously because they summarize multimodal SCM distributions, while explicit posterior means and medians remain continuous.

  2. Constructing g-computation estimators: two case studies in selection bias

    stat.ME 2025-06 conditional novelty 6.0 of 10

    New g-computation estimators, expressed as stacked estimating equations, recover average causal effects under treatment-induced selection and under confounding plus selection bias when no single adjustment set exists.

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