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Tanvi Shinkre

Publications and source records attributed to Tanvi Shinkre.

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Post-treatment problems: What can we say about the effect of a treatment among sub-groups who (would) respond in some way?

Investigators are often interested in how a treatment affects an outcome for units responding to treatment in a certain way. We may wish to know the effect among units that, for example, meaningfully implemented an intervention, passed an attention check, or demonstrated some important mechanistic response. Simply conditioning on the observed value of the post-treatment variable introduces problematic biases. Further, the identification assumptions required of several existing strategies are often indefensible. We propose the Treatment Reactive Average Causal Effect (TRACE), which we define as the total effect of treatment in the group that, if treated, would realize a particular value of the relevant post-treatment variable. By reasoning about the effect among the "non-reactive" group, we can identify and estimate the range of plausible values for the TRACE. We demonstrate the use of this approach with three examples: (i) learning the effect of police-perceived race on police violence during traffic stops, a case where point identification may be possible; (ii) estimating effects of a community-policing intervention in Liberia, in communities that meaningfully implemented it, and (iii) studying how in-person canvassing affects support for transgender rights, among participants for whom the intervention would result in more positive feelings towards transgender people.

stat.ME

Demystifying and avoiding the OLS "weighting problem": Unmodeled heterogeneity and straightforward solutions

Researchers frequently estimate treatment effects by regressing outcomes (Y) on treatment (D) and covariates (X). Even without unobserved confounding, the coefficient on D yields a conditional-variance-weighted average of strata-wise effects, not the average treatment effect. Scholars have proposed characterizing the severity of these weights, evaluating resulting biases, or changing investigators' target estimand to the conditional-variance-weighted effect. We aim to demystify these weights, clarifying how they arise, what they represent, and how to avoid them. Specifically, these weights reflect misspecification bias from unmodeled treatment-effect heterogeneity. Rather than diagnosing or tolerating them, we recommend avoiding the issue altogether, by relaxing the standard regression assumption of "single linearity" to one of "separate linearity" (of each potential outcome in the covariates), accommodating heterogeneity. Numerous methods--including regression imputation (g-computation), interacted regression, and mean balancing weights--satisfy this assumption. In many settings, the efficiency cost to avoiding this weighting problem altogether will be modest and worthwhile.

stat.ME