vignettes/did-basics.Rmd
did-basics.Rmd
This vignette discusses the basics of using Difference-in-Differences (DiD) designs to identify and estimate the average effect of participating in a treatment with a particular focus on tools from the did package. The background article for it is Callaway and Sant’Anna (2020), “Difference-in-Differences with Multiple Time Periods”.
The did package allows for multiple periods and variation in treatment timing
The did package allows the parallel trends assumption to hold conditional on covariates
Treatment effect estimates coming from the did package do not suffer from any of the drawbacks associated with two-way fixed effects regressions or event study regressions when there are multiple periods / variation in treatment timing
The did package can deliver disaggregated group-time average treatment effects as well as event-study type estimates (treatment effects parameters corresponding to different lengths of exposure to the treatment) and overall treatment effect estimates.
We use some notation in this vignette that is fully explained in our Introduction to DiD with Multiple Time Periods vignette.
Let’s start with a really simple example with simulated data. Here, there are going to be 4 time periods. There are 4000 units in the treated group that are randomly (with equal probability) assigned to first participate in the treatment (a group) in each time period. And there are 4000 ``never treated’’ units. The data generating process for untreated potential outcomes
\[ Y_{it}(0) = \theta_t + \eta_i + X_i'\beta_t + v_{it} \]
This is an example of a very simple model for untreated potential outcomes that is compatible with a conditional parallel trends assumption. In particular,
We consider the case where \(\eta_i\) can be distributed differently across groups. This means that comparisons of outcomes in levels between treated and untreated units will not deliver an average treatment effect parameter.
Next, notice that \[ \Delta Y_{it}(0) = (\theta_t - \theta_{t-1}) + X_i'(\beta_t - \beta_{t-1}) + \Delta v_{it} \]
so that the path of outcomes depends on covariates. And, in general, unconditional parallel trends is not valid in this setup unless either (i) the mean of the covariates is the same across groups (e.g., when treatment groups are independent of covariates), or (ii) \(\beta_t = \beta_{t-1} = \cdots = \beta_{1}\) (this is the case when the path of untreated potential outcomes doesn’t actually depend on covariates).
In order to think about treatment effects, we also use the following stylized model for treated potential outcomes \[ Y_{it}(g) = Y_{it}(0) + \mathbf{1}\{t \geq g\} (e+1) + ( u_{it} - v_{it}) \]
where \(e := t-g\) is the event time (i.e., the difference between the current time period and the time when a unit becomes treated), and the last term just allows for the error terms to be different for treated and untreated potential outcomes. It immediately follows that, in this particular example, \[ATT(g,t) = e+1\] for all post-treatment periods \(t \ge g\).
In other words, the average effect of participating in the treatment for units in group \(g\) is equal to their length of exposure plus one. Note that, for simplicity, we are considering the case where treatment effects are homogeneous across groups. Also, in this setup, units do not anticipate their treatment status, so the no-anticipation assumption is also satisfied.
For the simulations, we also set
Building the dataset
# set seed so everything is reproducible
set.seed(1814)
# generate dataset with 4 time periods
time.periods <- 4
# add dynamic effects
te.e <- 1:time.periods
# generate data set with these parameters
# here, we dropped all units who are treated in time period 1 as they do not help us recover ATT(g,t)'s.
dta <- build_sim_dataset()
# How many observations remained after dropping the ``always-treated'' units
nrow(dta)
#> [1] 27952
#This is what the data looks like
head(dta)
#> G X id period Y treat
#> 1 2 0.530541 1 1 4.795125 1
#> 8001 2 0.530541 1 2 7.159789 1
#> 16001 2 0.530541 1 3 8.482624 1
#> 24001 2 0.530541 1 4 11.288278 1
#> 2 4 1.123550 2 1 4.375698 1
#> 8002 4 1.123550 2 2 9.285481 1
Estimating Group-Time Average Treatment Effects
The main function to estimate group-time average treatment effects is the att_gt
function. See documentation here. The most basic call to att_gt
is given in the following
# estimate group-time average treatment effects using att_gt method
example_attgt <- att_gt(yname = "Y",
tname = "period",
idname = "id",
gname = "G",
xformla = ~X,
data = dta
)
# summarize the results
summary(example_attgt)
#>
#> Call:
#> att_gt(yname = "Y", tname = "period", idname = "id", gname = "G",
#> xformla = ~X, data = dta)
#>
#> Reference: Callaway, Brantly and Pedro H.C. Sant'Anna. "Difference-in-Differences with Multiple Time Periods." Forthcoming at the Journal of Econometrics <https://arxiv.org/abs/1803.09015>, 2020.
#>
#> Group-Time Average Treatment Effects:
#> Group Time ATT(g,t) Std. Error [95% Simult. Conf. Band]
#> 2 2 0.9615 0.0593 0.8035 1.1196 *
#> 2 3 2.0424 0.0587 1.8859 2.1989 *
#> 2 4 3.0104 0.0601 2.8503 3.1705 *
#> 3 2 -0.0392 0.0551 -0.1862 0.1077
#> 3 3 1.0877 0.0617 0.9233 1.2522 *
#> 3 4 1.9938 0.0589 1.8369 2.1506 *
#> 4 2 -0.0537 0.0585 -0.2096 0.1022
#> 4 3 0.0382 0.0563 -0.1119 0.1883
#> 4 4 0.9410 0.0578 0.7869 1.0951 *
#> ---
#> Signif. codes: `*' confidence band does not cover 0
#>
#> P-value for pre-test of parallel trends assumption: 0.79243
#> Control Group: Never Treated, Anticipation Periods: 0
#> Estimation Method: Doubly Robust
The summary of example_attgt
provides estimates of the group-time average treatment effects in the column labeled att
, and the corresponding bootstrapped-based standard errors are given in the column se
. The corresponding groups and times are given in the columns group
and time
. Under the no-anticipation and parallel trends assumptions, group-time average treatment effects are identified in periods when \(t \geq g\) (i.e., post-treatment periods for each group). The table also reports pseudo group-time average treatment effects when \(t < g\) (i.e., pre-treatment periods for group \(g\)). These can be used as a pre-test for the parallel trends assumption (as long as we assume that the no-anticipation assumption indeed holds). In addition, the results of a Wald pre-test of the parallel trends assumption is reported in the summary of the results. A much more detailed discussion of using the did package for pre-testing is available here.
Next, we’ll demonstrate how to plot group-time average treatment effects. To plot these, use the ggdid
function which builds off the ggplot2
package.
# plot the results
ggdid(example_attgt)
The resulting figure is one that contains separate plots for each group. Notice in the figure above, the first plot is labeled “Group 2”, the second “Group 3”, etc. Then, the figure contains estimates of group-time average treatment effects for each group in each time period along with a simultaneous confidence interval. The red dots in the plots are pre-treatment pseudo group-time average treatment effects and are most useful for pre-testing the parallel trends assumption. The blue dots are post-treatment group-time average treatment effects and should be interpreted as the average effect of participating in the treatment for units in a particular group at a particular point in time.
did
packageThe above discussion covered only the most basic case for using the did
package. There are a number of simple extensions that are useful in applications.
By default, the did
package reports simultaneous confidence bands in plots of group-time average treatment effects with multiple time periods – these are confidence bands that are robust to multiple hypothesis testing [essentially, the idea here is to use the same standard errors but make an adjustment to the critical value to account for multiple testing – in the example in this section, the critical value for a 95% uniform confidence band is 2.66 instead of 1.96]. You can turn this off and compute analytical standard errors and corresponding figures with pointwise confidence intervals by setting bstrap=FALSE, cband=FALSE
in the call to att_gt
…but we don’t recommend it!
In many applications, there can be a large number of groups and time periods. In this case, it may be infeasible to interpret plots of group-time average treatment effects. The did
package provides a number of ways to aggregate group-time average treatment effects using the aggte
function.
One idea that is likely to immediately come to mind is to just return a weighted average of all group-time average treatment effects with weights proportional to the group size. This is available by calling the aggte
function with type = simple
.
agg.simple <- aggte(example_attgt, type = "simple")
summary(agg.simple)
#>
#> Call:
#> aggte(MP = example_attgt, type = "simple")
#>
#> Reference: Callaway, Brantly and Pedro H.C. Sant'Anna. "Difference-in-Differences with Multiple Time Periods." Forthcoming at the Journal of Econometrics <https://arxiv.org/abs/1803.09015>, 2020.
#>
#>
#> ATT Std. Error [ 95% Conf. Int.]
#> 1.6557 0.0317 1.5937 1.7178 *
#>
#>
#> ---
#> Signif. codes: `*' confidence band does not cover 0
#>
#> Control Group: Never Treated, Anticipation Periods: 0
#> Estimation Method: Doubly Robust
This sort of aggregation immediately avoids the negative weights issue that two-way fixed effects regressions can suffer from, but we often think that there are better alternatives. In particular, this simple
aggregation tends to overweight the effect of early-treated groups simply because we observe more of them during post-treatment periods. We think there are likely to be better alternatives in most applications.
One of the most common alternative approaches is to aggregate group-time effects into an event study plot. Group-time average treatment effects can immediately be averaged into average treatment effects at different lengths of exposure to the treatment using the following code:
agg.es <- aggte(example_attgt, type = "dynamic")
summary(agg.es)
#>
#> Call:
#> aggte(MP = example_attgt, type = "dynamic")
#>
#> Reference: Callaway, Brantly and Pedro H.C. Sant'Anna. "Difference-in-Differences with Multiple Time Periods." Forthcoming at the Journal of Econometrics <https://arxiv.org/abs/1803.09015>, 2020.
#>
#>
#> Overall summary of ATT’s based on event-study/dynamic aggregation:
#> ATT Std. Error [ 95% Conf. Int.]
#> 2.0086 0.0346 1.9408 2.0763 *
#>
#>
#> Dynamic Effects:
#> Event time Estimate Std. Error [95% Simult. Conf. Band]
#> -2 -0.0537 0.0593 -0.2031 0.0956
#> -1 -0.0011 0.0370 -0.0944 0.0923
#> 0 0.9988 0.0300 0.9231 1.0744 *
#> 1 2.0166 0.0403 1.9150 2.1181 *
#> 2 3.0104 0.0599 2.8594 3.1613 *
#> ---
#> Signif. codes: `*' confidence band does not cover 0
#>
#> Control Group: Never Treated, Anticipation Periods: 0
#> Estimation Method: Doubly Robust
ggdid(agg.es)
In this figure, the x-axis is the length of exposure to the treatment. Length of exposure equal to 0 provides the average effect of participating in the treatment across groups in the time period when they first participate in the treatment (instantaneous treatment effect). Length of exposure equal to -1 corresponds to the time period before groups first participate in the treatment, and length of exposure equal to 1 corresponds to the first time period after initial exposure to the treatment.
As we would expect based on the data that we generated, it looks like parallel trends holds in pre-treatment periods and the effect of participating in the treatment is increasing with length of exposure of the treatment.
The Overall ATT here averages the average treatment effects across all lengths of exposure to the treatment.
Another idea is to look at average effects specific to each group. It is also straightforward to aggregate group-time average treatment effects into group-specific average treatment effects using the following code:
agg.gs <- aggte(example_attgt, type = "group")
summary(agg.gs)
#>
#> Call:
#> aggte(MP = example_attgt, type = "group")
#>
#> Reference: Callaway, Brantly and Pedro H.C. Sant'Anna. "Difference-in-Differences with Multiple Time Periods." Forthcoming at the Journal of Econometrics <https://arxiv.org/abs/1803.09015>, 2020.
#>
#>
#> Overall summary of ATT’s based on group/cohort aggregation:
#> ATT Std. Error [ 95% Conf. Int.]
#> 1.4801 0.0293 1.4227 1.5375 *
#>
#>
#> Group Effects:
#> Group Estimate Std. Error [95% Simult. Conf. Band]
#> 2 2.0048 0.0493 1.8915 2.1181 *
#> 3 1.5407 0.0483 1.4297 1.6517 *
#> 4 0.9410 0.0580 0.8077 1.0743 *
#> ---
#> Signif. codes: `*' confidence band does not cover 0
#>
#> Control Group: Never Treated, Anticipation Periods: 0
#> Estimation Method: Doubly Robust
ggdid(agg.gs)
In this figure, the y-axis is categorized by group. The x-axis provides estimates of the average effect of participating in the treatment for units in each group averaged across all time periods after that group becomes treated. In our example, the average effect of participating in the treatment is largest for group 2 – this is because the effect of treatment here increases with length of exposure to the treatment, and they are the group that is exposed to the treatment for the longest.
The Overall ATT averages the group-specific treatment effects across groups. In our view, this parameter is a leading choice as an overall summary effect of participating in the treatment. It is the average effect of participating in the treatment that was experienced across all units that participate in the treatment in any period. In this sense, it has a similar interpretation to the ATT in the textbook case where there are exactly two periods and two groups.
Finally, the did
package allows aggregations across different time periods. To do this
agg.ct <- aggte(example_attgt, type = "calendar")
summary(agg.ct)
#>
#> Call:
#> aggte(MP = example_attgt, type = "calendar")
#>
#> Reference: Callaway, Brantly and Pedro H.C. Sant'Anna. "Difference-in-Differences with Multiple Time Periods." Forthcoming at the Journal of Econometrics <https://arxiv.org/abs/1803.09015>, 2020.
#>
#>
#> Overall summary of ATT’s based on calendar time aggregation:
#> ATT Std. Error [ 95% Conf. Int.]
#> 1.4822 0.0336 1.4164 1.548 *
#>
#>
#> Time Effects:
#> Time Estimate Std. Error [95% Simult. Conf. Band]
#> 2 0.9615 0.0591 0.8163 1.1067 *
#> 3 1.5353 0.0475 1.4184 1.6521 *
#> 4 1.9498 0.0407 1.8498 2.0498 *
#> ---
#> Signif. codes: `*' confidence band does not cover 0
#>
#> Control Group: Never Treated, Anticipation Periods: 0
#> Estimation Method: Doubly Robust
ggdid(agg.ct)
In this figure, the x-axis is the time period and the estimates along the y-axis are the average effect of participating in the treatment in a particular time period for all groups that participated in the treatment in that time period.
Small group sizes can sometimes cause estimation problems in the did
package. To give an example, if there are any groups that have fewer observations than the number of covariates in the model, the code will error. The did
package reports a warning if there are any groups that have fewer than 5 observations.
In addition, statistical inference, particularly on group-time average treatment may become more tenuous with small groups. For example, the effective sample size for estimating the change in outcomes over time for individuals in a particular group is equal to the number of observations in that group and asymptotic results are unlikely to provide good approximations to the sampling distribution of group-time average treatment effects when the number of units in a group is small. In these cases, one should be very cautious about interpreting the \(ATT(g,t)\) results for these small groups.
A reasonable alternative approach in this case is to just focus on aggregated treatment effect parameters (i.e., to run aggte(..., type = "group")
or aggte(...,type = "dynamic")
). For each of these cases, the effective sample size is the total number of units that are ever treated. As long as the total number of ever treated units is “large” (which should be the case for many DiD application), then the statistical inference results provided by the did
package should be more stable.
By default, the did
package uses the group of units that never participate in the treatment as the control group. In this case, if there is no group that never participates, then the did
package will drop the last period and set units that do not become treated until the last period as the control group (this will also throw a warning). The other option for the control group is to use the “not yet treated”. The “not yet treated” include the never treated as well as those units that, for a particular point in time, have not been treated yet (though they eventually become treated). This group is at least as large as the never treated group though it changes across time periods. To use the “not yet treated” as the control, set the option control_group="notyettreated"
.
The did
package can also work with repeated cross section rather than panel data. If the data is repeated cross sections, simply set the option panel = FALSE
. In this case, idname
is also ignored. From a usage standpoint, everything else is identical to the case with panel data.
By default, the did
package takes in panel data and, if it is not balanced, coerces it into being a balanced panel by dropping units with observations that are missing in any time period. However, if the user specifies the option allow_unbalanced_panel = TRUE
, then the did
package will not coerce the data into being balanced. Practically, the main cost here is that the computation time will increase in this case. We also recommend that users think carefully about why they have an unbalanced panel before proceeding this direction.
The did
package implements all the \(2 \times 2\) DiD estimators that are in the DRDID
package. By default, the did
package uses “doubly robust” estimators that are based on first step linear regressions for the outcome variable and logit for the generalized propensity score. The other options are “ipw” for inverse probability weighting and “reg” for regression.
example_attgt_reg <- att_gt(yname = "Y",
tname = "period",
idname = "id",
gname = "G",
xformla = ~X,
data = data,
est_method = "reg"
)
summary(example_attgt_reg)
The argument est_method
is also available to pass in a custom function for estimating DiD with 2 periods and 2 groups. See its documentation for more details. Fair Warning: this is very advanced use of the did
package and should be done with caution.
Next, we use a subset of data that comes from Callaway and Sant’Anna (2020). This is a dataset that contains county-level teen employment rates from 2003-2007. The data can be loaded by
data(mpdta)
mpdta
is a balanced panel with 2500 observations. And the dataset looks like
head(mpdta)
#> year countyreal lpop lemp first.treat treat
#> 866 2003 8001 5.896761 8.461469 2007 1
#> 841 2004 8001 5.896761 8.336870 2007 1
#> 842 2005 8001 5.896761 8.340217 2007 1
#> 819 2006 8001 5.896761 8.378161 2007 1
#> 827 2007 8001 5.896761 8.487352 2007 1
#> 937 2003 8019 2.232377 4.997212 2007 1
Data Requirements
In particular applications, the dataset should look like this with the key parts being:
The dataset should be in long format – each row corresponds to a particular unit at a particular point in time. Sometimes panel data is in wide format – each row contains all the information about a particular unit in all time periods. To convert from wide to long in R
, one can use the tidyr::pivot_longer
function. Here is an example
There needs to be an id variable. In mpdta
, it is the variable countyreal
. This should not vary over time for particular units. The name of this variable is passed to methods in the did
package by setting, for example, idname = "countyreal"
There needs to be a time variable. In mpdta
, it is the variable year
. The name of this variable is passed to methods in the did
package by setting, for example, tname = "year"
In this application, the outcome is lemp
. The name of this variable is passed to methods in the did
package by setting, for example, yname = "lemp"
There needs to be a group variable. In mpdta
, it is the variable first.treat
. This is the time period when an individual first becomes treated. For individuals that are never treated, this variable should be set equal to 0. The name of this variable is passed to methods in the did
package by setting, for example, gname = "first.treat"
The did
package allows for incorporating covariates so that the parallel trends assumption holds only after conditioning on these covariates. In mpdta
, lpop
is the log of county population. The did
package requires that covariates be time-invariant. For time varying covariates like county population, the did
package sets the value of the covariate to be equal to the value of the covariate in the first time period. Covariates are passed as a formula to the did
package by setting, for example, xformla = ~lpop
. For estimators under unconditional parallel trends, the xformla
argument can be left blank or can be set as xformla = ~1
to only include a constant.
Next, we walk through a straightforward, but realistic way to use the did
package to carry out an application.
Side Comment: This is just an example of how to use our method in a real-world setup. To really evaluate the effect of the minimum wage on teen employment, one would need to be more careful along a number of dimensions. Thus, results displayed here should be interpreted as illustrative only.
We’ll consider two cases. For the first case, we will not condition on any covariates. For the second, we will condition on the log of county population (in a “real” application, one might want to condition on more covariates).
# estimate group-time average treatment effects without covariates
mw.attgt <- att_gt(yname = "lemp",
gname = "first.treat",
idname = "countyreal",
tname = "year",
xformla = ~1,
data = mpdta,
)
# summarize the results
summary(mw.attgt)
#>
#> Call:
#> att_gt(yname = "lemp", tname = "year", idname = "countyreal",
#> gname = "first.treat", xformla = ~1, data = mpdta)
#>
#> Reference: Callaway, Brantly and Pedro H.C. Sant'Anna. "Difference-in-Differences with Multiple Time Periods." Forthcoming at the Journal of Econometrics <https://arxiv.org/abs/1803.09015>, 2020.
#>
#> Group-Time Average Treatment Effects:
#> Group Time ATT(g,t) Std. Error [95% Simult. Conf. Band]
#> 2004 2004 -0.0105 0.0240 -0.0763 0.0553
#> 2004 2005 -0.0704 0.0316 -0.1569 0.0161
#> 2004 2006 -0.1373 0.0373 -0.2394 -0.0351 *
#> 2004 2007 -0.1008 0.0346 -0.1957 -0.0059 *
#> 2006 2004 0.0065 0.0224 -0.0549 0.0679
#> 2006 2005 -0.0028 0.0191 -0.0551 0.0496
#> 2006 2006 -0.0046 0.0190 -0.0566 0.0474
#> 2006 2007 -0.0412 0.0202 -0.0967 0.0142
#> 2007 2004 0.0305 0.0146 -0.0096 0.0707
#> 2007 2005 -0.0027 0.0165 -0.0480 0.0425
#> 2007 2006 -0.0311 0.0173 -0.0784 0.0163
#> 2007 2007 -0.0261 0.0174 -0.0738 0.0217
#> ---
#> Signif. codes: `*' confidence band does not cover 0
#>
#> P-value for pre-test of parallel trends assumption: 0.16812
#> Control Group: Never Treated, Anticipation Periods: 0
#> Estimation Method: Doubly Robust
# plot the results
# set ylim so that all plots have the same scale along y-axis
ggdid(mw.attgt, ylim = c(-.3,.3))
There are a few things to notice in this case
There does not appear to be much evidence against the parallel trends assumption. One fails to reject using the Wald test reported in summary
; likewise the uniform confidence bands cover 0 in all pre-treatment periods.
There is some evidence of negative effects of the minimum wage on employment. Two group-time average treatment effects are negative and statistically different from 0. These results also suggest that it may be helpful to aggregate the group-time average treatment effects.
# aggregate the group-time average treatment effects
mw.dyn <- aggte(mw.attgt, type = "dynamic")
summary(mw.dyn)
#>
#> Call:
#> aggte(MP = mw.attgt, type = "dynamic")
#>
#> Reference: Callaway, Brantly and Pedro H.C. Sant'Anna. "Difference-in-Differences with Multiple Time Periods." Forthcoming at the Journal of Econometrics <https://arxiv.org/abs/1803.09015>, 2020.
#>
#>
#> Overall summary of ATT’s based on event-study/dynamic aggregation:
#> ATT Std. Error [ 95% Conf. Int.]
#> -0.0772 0.0208 -0.1181 -0.0364 *
#>
#>
#> Dynamic Effects:
#> Event time Estimate Std. Error [95% Simult. Conf. Band]
#> -3 0.0305 0.0152 -0.0072 0.0682
#> -2 -0.0006 0.0135 -0.0339 0.0328
#> -1 -0.0245 0.0139 -0.0588 0.0099
#> 0 -0.0199 0.0119 -0.0495 0.0096
#> 1 -0.0510 0.0173 -0.0937 -0.0082 *
#> 2 -0.1373 0.0438 -0.2457 -0.0289 *
#> 3 -0.1008 0.0341 -0.1854 -0.0163 *
#> ---
#> Signif. codes: `*' confidence band does not cover 0
#>
#> Control Group: Never Treated, Anticipation Periods: 0
#> Estimation Method: Doubly Robust
ggdid(mw.dyn, ylim = c(-.3,.3))
These continue to be simultaneous confidence bands for dynamic effects. The results are broadly similar to the ones from the group-time average treatment effects: one fails to reject parallel trends in pre-treatment periods and it looks like somewhat negative effects of the minimum wage on youth employment.
One potential issue with these dynamic effect estimators is that the composition of the groups changes with different lengths of exposure in the event study plots. For example, for the group of states who increased their minimum wage in 2007, we can only identify the instantaneous average effect of the minimum wage (\(e=0\)), whereas for states that raised their minimum wage in 2004 (2006), we can identify the average effect of the minimum wage on event-times \(e=0,1,2,3\) (\(e=0,1\)). When computing the event-study plot for \(e=0\), we would aggregate the effects for all three groups, but this is not the case when \(e=1,2,3\). If the effects of the minimum wage are systematically different across groups (here, there is not much evidence of this as the effect for all groups seems to be close to 0 on impact and perhaps becoming more negative over time), then this can lead to confounding dynamics and selective treatment timing among different groups.
One way to combat this is to balance the sample by (i) only including groups that are exposed to the treatment for at least a certain number of time periods and (ii) only look at dynamic effects in those time periods. In the did
package, one can do this by specifying the balance_e
option. Here, we set balance_e = 1
– what this does is to only consider groups of states that are treated in 2004 and 2006 (so we can compute event-study-type parameters for them for \(e=0,1\)), drops the group treated in 2007 (as we can not compute the event-study-type parameter with \(e=1\) for this group)), and then only looks at instantaneous average effects and the average effect one period after states raised the minimum wage.
mw.dyn.balance <- aggte(mw.attgt, type = "dynamic", balance_e=1)
summary(mw.dyn.balance)
#>
#> Call:
#> aggte(MP = mw.attgt, type = "dynamic", balance_e = 1)
#>
#> Reference: Callaway, Brantly and Pedro H.C. Sant'Anna. "Difference-in-Differences with Multiple Time Periods." Forthcoming at the Journal of Econometrics <https://arxiv.org/abs/1803.09015>, 2020.
#>
#>
#> Overall summary of ATT’s based on event-study/dynamic aggregation:
#> ATT Std. Error [ 95% Conf. Int.]
#> -0.0288 0.0137 -0.0556 -0.0019 *
#>
#>
#> Dynamic Effects:
#> Event time Estimate Std. Error [95% Simult. Conf. Band]
#> -2 0.0065 0.0247 -0.0534 0.0665
#> -1 -0.0028 0.0194 -0.0498 0.0443
#> 0 -0.0066 0.0144 -0.0414 0.0283
#> 1 -0.0510 0.0180 -0.0946 -0.0073 *
#> ---
#> Signif. codes: `*' confidence band does not cover 0
#>
#> Control Group: Never Treated, Anticipation Periods: 0
#> Estimation Method: Doubly Robust
ggdid(mw.dyn.balance, ylim = c(-.3,.3))
Finally, we can run all the same results including a covariate. In this application the results turn out to be nearly identical, and here we provide just the code for estimating the group-time average treatment effects while including covariates. The other steps are otherwise the same.
mw.attgt.X <- att_gt(yname = "lemp",
gname = "first.treat",
idname = "countyreal",
tname = "year",
xformla = ~lpop,
data = mpdta,
)
We update this section with common issues that people run into when using the did
package. Please feel free to contact us with questions or comments.
did
package is only built to handle staggered treatment adoption designs. This means that once an individual becomes treated, they remain treated in all subsequent periods.