In this final post we outline the typical flow of a causal study in relation to the main tools provided by Causalinference. At a high level, assuming that unconfoundedness holds true in the given problem, we can break down a typical study into two phases.
In the design phase, we inspect and manipulate the data set to ensure that the most credible analysis can be conducted on it. We achieve this by proceeding in the following steps:
summary_stats
. If the normalized differences in covariate means suggest severe covariate imbalance, we can try to address it by using the propensity-score-based techniques below.est_propensity_s
, so that the following two propensity methods can be employed.trim_s
to exclude subjects with extreme propensity scores. Since very little can be credibly said about such units, we should focus attention on the remaining units that exhibit a higher degree of covariate balance.stratify_s
to group similar subjects together and improve within-bin covariate balance.In the analysis phase, we estimate treatment effects using a number of reasonable estimators. The estimators with the most desirable properties are
est_via_blocking
, which aggregates the least squares estimates within each propensity bin to produce an overall average treatment effect estimate.est_via_matching
, which pairs subjects together via nearest-neighborhood matching to arrive at an overall average treatment effect estimate. Since bias can result when the matching is imperfect, bias correction is recommended.If the design phase is done well, the two estimates recommended above should result in similar estimates due to their stability properties.
We conclude by noting that additional checks and tests exist for assessing the validity of a causal study. Some of these tests (e.g. for assessing the unconfoundedness assumption) actually require no additional tools beyond what is provided in Causalinference. For the interested reader, please refer to Imbens (2014).
Imbens, G. (2014). Matching methods in practice: Three examples. NBER Working Paper No. 19959.