Optimal Designs with Robust Inference for Binary Treatment Effects
二元结局处理效应的最优实验设计与稳健推断AI 解读 ↓
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We study randomized experiments with binary outcomes under Neyman's nonparametric model, where covariate measurements are fixed but potential outcomes are random. In this setting we derive the exact variance of the difference-in-means estimator and characterize designs that minimize it. We show that any balanced design satisfying a covariate-balance condition is asymptotically optimal, and we prove that a broad class of blocking designs satisfies this condition under mild smoothness assumptions. Because the variance depends on unknown success probabilities, unbiased variance estimation is impossible. We therefore develop two conservative estimators: a generalization of the Cochran-Mantel-Haenszel (CMH) statistic applicable to any balanced design, and an extension of Robins' variance estimator for blocking designs. We establish conditions under which the CMH-based estimator is asymptotically tight under local alternatives, thereby yielding asymptotically valid confidence intervals. Our theoretical and simulations results show that blocking and other designs that achieve covariate balance and sufficient degree of randomness, perform well when they are equipped with the CMH-based inference. Thus, we provide an experimental design and inference framework for incidence outcomes that is simultaneously variance-optimal, conservative in finite samples and asymptotically tight.
We study difference-in-differences designs in which all units are initially untreated and later receive heterogeneous, strictly positive treatment doses. When quasi-untreated units receive doses close to zero, a difference-in-difference estimand using those units as the control group identifies a weighted average treatment effect per unit of treatment, under a parallel-trends assumption. We develop a nonparametric estimator and bias-corrected confidence intervals for this…
伪面板事件研究:可信应用的计量经济学基础
Event studies with panel data are widely used to estimate treatment effects. With repeated cross-sections, future treatment dates are unobserved for untreated individuals. Pseudo-panel event studies impute pre-treatment outcomes of the treated using matched untreated individuals. This paper establishes identification in such designs and characterizes bias when identification conditions fail. I show that the pseudo-panel regression is equivalent to weighted least squares with…
嵌套工具变量分析:转换者平均处理效应及可推广性
Instrumental variables (IVs) are widely used to estimate causal effects from non-randomized data. A canonical example is a randomized trial with noncompliance, in which the randomized treatment assignment serves as an IV for the non-ignorable treatment received. Under a monotonicity assumption, a valid IV nonparametrically identifies the average treatment effect among a latent complier subgroup, whose generalizability is often under debate. In many studies, there exist…
We study nonparametric inference for a continuous-treatment causal dose-response curve and its first derivative under unmeasured confounding, using treatment- and outcome-inducing proxies. We establish a proximal doubly robust pseudo-outcome whose conditional mean given treatment equals the dose-response curve whenever either bridge function is correctly specified. Their (smoothed) efficient influence function representations lead to cross-fitted local-polynomial estimators…
平均处理效应局部化:合成控制中的投影方法
Many real-world policies and business interventions require assessing short-term effects to inform timely decisions, even though most causal inference methods focus on long-term average treatment effects. In this article, we introduce average treatment effect localization (ATEL), which captures localized, short-term policy impacts in panel data settings with a single treated unit and provides early indicators of policy impact. To accommodate both time-varying and nonlinear…
利用辅助事件信息进行删失结局的因果推断
Clinical trials with survival endpoints lose information when participants are censored before death is observed. We develop target-preserving estimators that use posttreatment disease history, such as recurrence or progression, to recover information lost to censoring for marginal survival and restricted mean survival effects. The difficulty is that the intermediate event is downstream of treatment: naive adjustment can change the causal estimand, and the useful information…