Misspecified Z-estimation and OLS with mixed (random+fixed) regressors yield conservative robust SEs and identify causal ATEs under randomization, with corrections for fully-interacted specs and clustered data.
Standard errors when a regressor is randomly assigned
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abstract
We examine asymptotic properties of the OLS estimator when the values of the regressor of interest are assigned randomly and independently of other regressors. We find that the OLS variance formula in this case is often simplified, sometimes substantially. In particular, when the regressor of interest is independent not only of other regressors but also of the error term, the textbook homoskedastic variance formula is valid even if the error term and auxiliary regressors exhibit a general dependence structure. In the context of randomized controlled trials, this conclusion holds in completely randomized experiments with constant treatment effects. When the error term is heteroscedastic with respect to the regressor of interest, the variance formula has to be adjusted not only for heteroscedasticity but also for correlation structure of the error term. However, even in the latter case, some simplifications are possible as only a part of the correlation structure of the error term should be taken into account. In the context of randomized control trials, this implies that the textbook homoscedastic variance formula is typically not valid if treatment effects are heterogenous but heteroscedasticity-robust variance formulas are valid if treatment effects are independent across units, even if the error term exhibits a general dependence structure. In addition, we extend the results to the case when the regressor of interest is assigned randomly at a group level, such as in randomized control trials with treatment assignment determined at a group (e.g., school/village) level.
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Misspecified regressions with mixed regressors: robust inference and causal interpretation
Misspecified Z-estimation and OLS with mixed (random+fixed) regressors yield conservative robust SEs and identify causal ATEs under randomization, with corrections for fully-interacted specs and clustered data.