Adaptive Experimental Design Using Shrinkage Estimators
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In multi-armed trials, adaptive designs are a popular way to increase estimation efficiency or identify optimal treatments. Several recent papers have proposed adaptive variants of the classical Neyman allocation to assign treatments in sequential trials, with the goal of minimizing the error of a Horvitz-Thompson-style estimator. However, this approach may be inefficient, because it fails to borrow information across the treatment arms. In this paper, we consider adaptivity in a sequential trial with K active treatments and a control, and suggest the use of Stein-like shrinkage estimators to obtain the final causal estimates. These estimators share information across arms, yielding provable reductions in expected squared error loss relative to estimating each causal effect in isolation. Moreover, for each of our candidate shrinkers, the risk is the expectation of ratios of Gaussian quadratic forms, and can be computed efficiently via numerical integration. Hence, we suggest a simple algorithm for sequential adaptivity: assign treatments to each new arrival by choosing the arm that will minimize the estimated shrinker loss. Through simulations, we demonstrate that this approach can yield meaningful reductions in estimation error, especially in the low signal-to-noise regime. We also characterize how our adaptive algorithm assigns treatments differently than would a sequential Neyman allocation, and suggest a method for constructing shorter confidence intervals at the trial's conclusion.
Two frequent approaches for identifying structural VARs are external instruments, which carry economic content but are often weak, and non-Gaussianity of the shocks, which provides statistical identification but carries no economic meaning. We combine the two strategies in a single generalized method of moments framework. This hybrid approach point-identifies the target shocks while also identifying the non-target shocks up to sign and ordering. Under suitable rank…
The conditional average treatment effect (CATE) is frequently estimated in clinical studies to refute a homogeneous treatment effect hypothesis. Under this regime, all patients making up the population experience identical benefit from a given treatment relative to a comparator. Uncovering heterogeneous treatment effects through inference about the CATE, however, requires that covariates truly modifying the treatment effect be reliably collected at baseline. CATE-based…
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A standard assumption in the Bayesian estimation of linear regression models is that the regressors are exogenous in the sense that they are uncorrelated with the model error term. In practice, however, this assumption can be invalid. In this article, using the exponentially tilted empirical likelihood (ETEL) framework, we develop a Bayes factor test for endogeneity that compares a base model that is correctly specified under exogeneity but misspecified under endogeneity…
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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…
自适应实验中策略改进价值的推断
In this paper, we develop an asymptotically normal estimator for the value of policy improvement (VPI) under adaptively collected data. This value, which is defined as the gap between the value of the best treatment policy in a class and that of a baseline policy, gauges whether or not it is worth deploying a personalized treatment policy. Building an estimator for the VPI is naturally more difficult than estimating the value of a fixed policy. This is because, in addition…