EquiTrends

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EquiTrends is an R package for equivalence testing in the context of Difference-in-Differences estimation. It allows users to test if pre-treatment trends in the treated group are “equivalent” to those in the control group. Here, “equivalence” means that rejection of the null hypothesis implies that a function of the pre-treatment placebo effects (maximum absolute, average or root mean squared value) does not exceed a pre-specified threshold below which trend differences are considered negligible. The package is based on the theory developed in Dette & Schumann (2024).

The package contains the functions maxEquivTest to perform the testing procedure surrounding the maximum placebo coefficient (see equation (3.1) of Dette & Schumann (2024)), meanEquivTest to perform the testing procedure surrounding the mean placebo coefficient (see equation (3.2) of Dette & Schumann (2024)) and rmsEquivTest to perform the testing procedure surrounding the root mean squared placebo coefficient (see equation (3.3) and (3.4) of Dette & Schumann (2024)). Furthermore, the package contains the function sim_paneldata to simulate a paneldataset for such testing purposes.

Installation

You can install the development version of EquiTrends from GitHub with:

# install.packages("devtools")
devtools::install_github("TiesBos/EquiTrends")

Data Simulation

The EquiTrends package contains a function to simulate panel data, tailored to the Difference-in-Differences framework. The function sim_paneldata simulates a panel dataset with a given number of individuals \(N\) (N), number of periods \(T+1\) (in the setting of this package, indicating the number of pre-treatment periods. In sim_paneldata \(T+1\) is referred to as tt), number of covariates \(p\) (p), and treatment effects. Typically, period \(T+1\) is referred to as the “base period”. The function also allows for the simulation of heterogeneity in treatment effects (specified through eta) and time fixed effects (through lambda). Furthermore, the function allows for heteroscedasticty (specified through the binary variable het), serial correlation (through the AR(1) coefficient phi: \(u_{i,t} = \phi u_{i,t-1} + v_{i,t}\) where \(v_{i,t}\) follows an i.i.d. \(N(0,\sigma^2)\) distribution and \(\sigma\) is specified through sd), and clustering in the model errors \(u_{i,t}\). The function returns a data frame with the following columns: ID (the cross-sectional individual identifier), period (the time identifier), Y (the dependent variable), G (a binary vector indicating if an individual receives treatment, indicated by 1, or not, indicated by 0), and X_1, X_2, …, X_p (additional control variables). The construction of the dependent variable follows the two-way fixed effect model, similar to the model in equation (2.5) of Dette & Schumann (2024):

\[Y_{i,t} = \eta_i + \lambda_t + \sum_{l=1}^{T}{\beta_l}G_iD_l(t) + X_{1, i, t}\gamma_1+ \dots + X_{p,i,t}\gamma_p +u_{i,t} \quad \text{with} \ \ i=1,...,N, \ \ t=1,...,T+1\]

where \(D_l(t)\) is a dummy variable that equals 1 if \(t=l\) and 0 otherwise. The error-terms \(u_{i,t}\) are generated through a normal distribution with mean 0 and a variance-covariance structure depending on the user-specified parameters. In the following, the \(\beta_l\) coefficients are referred to as placebo coefficients, since they represent the difference in pre-trends between the treatment and control group before treatment has been assigned.

An example of the sim_paneldata function is provided below:

library(EquiTrends)

# Simulate a panel dataset with 500 individuals, 5 periods, 2 additional 
# regressors, and a binary treatment variable without heteroscedasticity, 
# serial correlation, and clustering. Furthermore, there are no fixed effects or 
# pre-trends in the model (since all values in beta are 0).
sim_data <- sim_paneldata(N = 500, tt = 5, p = 2, beta = rep(0, 5), 
                          gamma = rep(1, 2), het = 0, phi = 0, sd = 1, 
                          burnins = 50)
head(sim_data)
#>   ID period          Y G        X_1          X_2
#> 1  1      1 -0.8123777 0 -0.4407095 -0.655157012
#> 2  1      2 -1.8888861 0 -0.2212108 -0.349846262
#> 3  1      3 -2.2912561 0 -0.9741446 -0.000781637
#> 4  1      4 -0.5314161 0  0.2259398 -1.557426790
#> 5  1      5 -1.5528134 0 -0.1413597 -1.590501621
#> 6  2      1  1.5202663 1 -0.1386675  1.074761245

The EquiTrends package contains functions to test for equivalence of pre-trends in Difference-in-Differences estimation. The functions rmsEquivTest, meanEquivTest, and maxEquivTest are used to test for equivalence of pre-trends in Difference-in-Differences estimation using the placebo coefficients \(\beta_{l} \ (l=1,...,T)\) estimates. The functions are based on the work of Dette & Schumann (2024).

The rmsEquivTest function

rmsEquivTest implements the equivalence testing procedure surrounding the root mean squared placebo coefficient as described in section 4.2.3 of Dette & Schumann (2024). The function tests the null hypothesis that the root mean squared placebo coefficient is larger than or equal to a user-specified equivalence threshold \(\delta\). That is, if

\[\beta_{RMS} = \sqrt{\frac{1}{T}\sum_{l=1}^{T} \beta_l^2},\]

the tested hypotheses can be represented as

\[H_0: \beta_{RMS} \geq \delta \quad \text{vs.} \quad H_1: \beta_{RMS} < \delta.\]

The null and alternative hypothesis can therefore be seen as non-negligible and negligible differences in pre-trends, respectively. The function returns an object of class rmsEquivTest containing

One should note that rows containing NA values are removed from the panel before the testing procedure is performed.

Please be aware that the equivalence test based on the root mean squared placebo coefficient applies a randomization technique (as described by Dette & Schumann (2024)), leading to a stochastic critical value and minimum equivalence threshold. Therefore, the results may vary between different runs of the function.

# Perform the equivalence test using an equivalence threshold of 1 with periods 
# 1-4 as pre-treatment periods based on the RMS testing procedure:
#  - option 1: using column names in the panel
# One can use the names of the columns in the panel to specify the variables:
rmsEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", X = c("X_1", "X_2"),
             data = sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
             base_period = 4)
#> 
#>                ==================================================
#>                Equivalence Tests for Pre-trends in DiD Estimation
#>                ==================================================
#> Type: Root Mean Squared Placebo Effect 
#> Significance level: 0.05 
#> Alternative hypothesis: the root mean squared placebo effect does not exceed the equivalence threshold of 1 .
#> ---
#> RMS Placebo Effect   Simulated Crit. Val.    Reject H0 
#> 0.1835               0.9558                  TRUE      
#> ---
#> No. placebo coefficients estimated: 3 
#> Base period: 4 
#>  
#> Balanced Panel: 
#>  + No. pre-treatment periods: 4 
#>  + No. individuals: 500 
#>  + Total no. observations: 2000
#  - option 2: using column numbers in the panel 
# Alternatively, one can use the column numbers in the panel to specify the variables:
rmsEquivTest(Y = 3, ID = 1, G = 4, period = 2, X = c(5, 6),
             data = sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
             base_period = 4)
             
#  - option 3: using separate variables 
# One can also use the variables directly without specifying the data variable:
data_Y <- sim_data$Y
data_ID <- sim_data$ID
data_G <- sim_data$G
data_period <- sim_data$period
data_X <- cbind(sim_data$X_1, sim_data$X_2)

rmsEquivTest(Y = data_Y, ID = data_ID, G = data_G, period = data_period, X = data_X,
             equiv_threshold = 1, pretreatment_period = 1:4,
             base_period = 4)

The testing procedures can also be performed without specifying the equivalence threshold. Then, the minimum equivalence threshold is returned for which the null hypothesis of non-negligible trend-differences can be rejected. Again, the three possible ways of entering the data as above can be used.

rmsEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", X = c("X_1", "X_2"),
             data = sim_data, equiv_threshold = NULL, pretreatment_period = 1:4,
             base_period = 4)
#> 
#>                ==================================================
#>                Equivalence Tests for Pre-trends in DiD Estimation
#>                ==================================================
#> Type: Root Mean Squared Placebo Effect 
#> Significance level: 0.05 
#> Alternative hypothesis: the root mean squared placebo effect does not exceed the equivalence threshold.
#> ---
#> RMS Placebo Effect   Min. Equiv. Threshold 
#> 0.1835               0.2558                
#> ---
#> No. placebo coefficients estimated: 3 
#> Base period: 4 
#>  
#> Balanced Panel: 
#>  + No. pre-treatment periods: 4 
#>  + No. individuals: 500 
#>  + Total no. observations: 2000

Finally, one should note that the test procedure also works for unbalanced panels.

# To illustrate this, we generate an unbalanced panel dataset by randomly selecting
# 70% of the observations from the balanced panel dataset:

random_indices <- sample(nrow(sim_data), 0.7*nrow(sim_data))
unbalanced_sim_data <- sim_data[random_indices, ]
#  With Equivalence Threshold:
rmsEquivTest(Y = 3, ID = 1, G = 4, period = 2, X = c(5, 6),
             data = unbalanced_sim_data, equiv_threshold = 1, 
             pretreatment_period = 1:4, base_period = 4)

#  Without Equivalence Threshold:
rmsEquivTest(Y = 3, ID = 1, G = 4, period = 2, X = c(5, 6),
             data = unbalanced_sim_data, equiv_threshold = NULL, 
             pretreatment_period = 1:4, base_period = 4)

The maxEquivTest function

The maxEquivTest function tests the null hypothesis that the maximum placebo coefficient is larger than or equal to a user-specified equivalence threshold \(\delta\). That is, if

\[\lVert\beta\rVert_\infty = \max_{l=1,...T} |\beta_l|,\]

the tested hypotheses can be represented as

\[H_0: \lVert\beta\rVert_\infty \geq \delta \quad \text{vs.} \quad H_1: \lVert\beta\rVert_\infty < \delta.\]

The null and alternative hypothesis can therefore be seen as non-negligible and negligible differences in pre-trends, respectively.

The function maxEquivTest contains three testing procedures for this test, as described in Section 4.2.1. of Dette & Schumann (2024). The function allows for the testing of the equivalence of pre-trends using a bootstrap for spherical errors (type = "Boot"), a wild bootstrap for clustered standard errors (type = "Wild"), and an Intersection Union approach (type = "IU") that rejects the null if all estimates for \(\beta_1,...,\beta_{T}\) are smaller than their individual critical values. The function returns an object of class maxEquivTestBoot if type = "Boot" or type = "Wild" or maxEquivTestIU if type = "IU". If no type is specified, maxEquivTest applies the Intersection Union procedure for efficiency reasons.

Implemention of the maxEquivTest function with type = "IU"

Examples of implementing the Intersection unit test with different possible variance-covariance matrices (required to perform the test) are provided below (for more information on the possible variance-covariance matrices, see the documentation of the maxEquivTest function). If an equivalence threshold is supplied, the function will test the previous hypothesis. If no equivalence threshold is supplied, the function finds the minimum equivalence threshold for which the null of non-negligible trend-differences can be reject using the Intersection Union test. The function returns an object of class maxEquivTestIU containing the following information:

One should note that rows containing NA values are removed from the panel before the testing procedure is performed.

# Perform the test with equivalent threshold specified as 1 based on 
# pre-treatment periods 1-4 and homoscedastic error-terms:
  # To select variables, one can use the column names / numbers in the panel data
maxEquivTest(Y = "Y", ID = "ID", G = "G", period = 2, X= c(5,6),
              data = sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
              base_period = 4, type = "IU")
#> 
#>                ==================================================
#>                Equivalence Tests for Pre-trends in DiD Estimation
#>                ==================================================
#> Type: Intersection Union 
#> Alternative hypothesis: the maximum placebo effect does not exceed the equivalence threshold of 1 .
#> Reject null hypothesis: TRUE 
#> ( Critical values are printed for the significance level: 0.05 )
#> ---
#> Abs. Estimate    Std. Error  Critical Value 
#> 0.09848          0.1221          0.7992        
#> 0.27253          0.1221          0.7992        
#> 0.13041          0.1220          0.7993        
#> ---
#> No. placebo coefficients estimated: 3 
#> Base period: 4 
#>  
#> Balanced Panel: 
#>  + No. pre-treatment periods: 4 
#>  + No. individuals: 500 
#>  + Total no. observations: 2000

  # Alternatively, one can enter the variables separately:
data_Y <- sim_data$Y
data_ID <- sim_data$ID
data_G <- sim_data$G
data_period <- sim_data$period
data_X <- sim_data[, c(5, 6)]
maxEquivTest(Y = data_Y, ID = data_ID, G = data_G, period = data_period, X = data_X,
             equiv_threshold = 1, pretreatment_period = 1:4,
             base_period = 4, type = "IU")
#> 
#>                ==================================================
#>                Equivalence Tests for Pre-trends in DiD Estimation
#>                ==================================================
#> Type: Intersection Union 
#> Alternative hypothesis: the maximum placebo effect does not exceed the equivalence threshold of 1 .
#> Reject null hypothesis: TRUE 
#> ( Critical values are printed for the significance level: 0.05 )
#> ---
#> Abs. Estimate    Std. Error  Critical Value 
#> 0.09848          0.1221          0.7992        
#> 0.27253          0.1221          0.7992        
#> 0.13041          0.1220          0.7993        
#> ---
#> No. placebo coefficients estimated: 3 
#> Base period: 4 
#>  
#> Balanced Panel: 
#>  + No. pre-treatment periods: 4 
#>  + No. individuals: 500 
#>  + Total no. observations: 2000
# Perform the test without specifying the equivalence threshold with heteroscedastic 
# and autocorrelation robust variance-covariance matrix estimator:
maxEquivTest(Y = 3, ID = 1, G = 4, period = 2, 
             data = sim_data, equiv_threshold = NULL, pretreatment_period = 1:4,
             base_period = 4, type = "IU", vcov = "HAC")
#> 
#>                ==================================================
#>                Equivalence Tests for Pre-trends in DiD Estimation
#>                ==================================================
#> Type: Intersection Union 
#> Significance level: 0.05 
#> Alternative hypothesis: the maximum placebo effect does not exceed the equivalence threshold.
#> Minimum equivalence threshold to accept the alternative: 0.4974 
#> ---
#>  Estimate    Std. Error   Minimum Equivalence Threshold 
#> 0.1028       0.2172      0.4489    
#> 0.1558       0.2088      0.4974    
#> 0.1257       0.2131      0.4711    
#> ---
#> No. placebo coefficients estimated: 3 
#> Base period: 4 
#>  
#> Balanced Panel: 
#>  + No. pre-treatment periods: 4 
#>  + No. individuals: 500 
#>  + Total no. observations: 2000
# Perform the test without specifying the equivalence threshold with a custom
# variance-covariance matrix estimator:
vcov_func <- function(x) {plm::vcovHC(x, method = "white1", type = "HC2")}
maxEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", 
             data = sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
             base_period = 4, type = "IU", vcov = vcov_func)
 
# Perform the test using clustered standard errors based on a vector indicating 
# the cluster. For instance, two clusters with the following rule: all
# individuals with an ID below 250 are in the same cluster.
cluster_ind <- ifelse(sim_data$ID < 250, 1, 2)
maxEquivTest(Y = data_Y, ID = data_ID, G = data_G, period = data_period, X = data_X,
               equiv_threshold = 1, pretreatment_period = 1:4,
               base_period = 4, type = "IU", vcov = "CL", cluster = cluster_ind)
#> Registered S3 method overwritten by 'clubSandwich':
#>   method    from    
#>   bread.mlm sandwich

Note that the testing procedure can also handle unbalanced panels.

# To illustrate this, we generate an unbalanced panel dataset by randomly selecting
# 70% of the observations from the balanced panel dataset:
random_indices <- sample(nrow(sim_data), 0.7*nrow(sim_data))
unbalanced_sim_data <- sim_data[random_indices, ]
maxEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", X = c(5, 6),
              data = unbalanced_sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
              base_period = 4, type = "IU", vcov = "HAC")
Implementation of the bootstrap approaches

Examples of implementing the bootstrap based test are provided below. For both type = "Boot" and type = "Wild", an equivalence threshold is required to perform the test. Furthermore, both testing procedures return an object of class “maxEquivTestBoot” containing

One should note that rows containing NA values are removed from the panel before the testing procedure is performed.

On top of that, please be aware that the bootstrap procedures for the equivalence test based on the maximum absolute placebo coefficient apply a bootstrap procedure (as described by Dette & Schumann (2024)), leading to a stochastic critical value and minimum equivalence threshold. Therefore, the results may vary slightly between different runs of the function.

The bootstrap for spherical errors with 1000 bootstrap iterations:

# Perform the test with equivalence threshold specified as 1 based on 
# pre-treatment periods 1:4 (with base period 4) with the general bootstrap procedure:
maxEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", 
             data = sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
             base_period = 4, type = "Boot", B = 1000)
#> 
#>                ==================================================
#>                Equivalence Tests for Pre-trends in DiD Estimation
#>                ==================================================
#> Type: Bootstrap for Spherical Errors  (Based on 1000 bootstrap samples)
#> Significance level: 0.05 
#> Alternative hypothesis: the maximum placebo effect does not exceed the equivalence threshold of 1 .
#> ---
#> Max. Abs. Coefficient    Bootstrap Critical Value    Reject H0 
#> 0.1558                   0.6586                      TRUE      
#> ---
#> No. placebo coefficients estimated: 3 
#> Base period: 4 
#>  
#> Balanced Panel:
#>  + No. pre-treatment periods: 4 
#>  + No. individuals: 500 
#>  + Total no. observations: 2000

The Wild boostrap with 1000 bootstrap iterations:

# Perform the test with the equivalence threshold specified as 1 based on 
# pre-treatment periods 1:4 (with base period 4) with the wild bootstrap procedure:
maxEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", 
             data = sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
             base_period = 4, type = "Wild")
#> 
#>                ==================================================
#>                Equivalence Tests for Pre-trends in DiD Estimation
#>                ==================================================
#> Type: Cluster Wild Bootstrap (Based on 1000 bootstrap samples)
#> Significance level: 0.05 
#> Alternative hypothesis: the maximum placebo effect does not exceed the equivalence threshold of 1 .
#> ---
#> Max. Abs. Coefficient    Bootstrap Critical Value    Reject H0 
#> 0.1558                   0.6642                      TRUE      
#> ---
#> No. placebo coefficients estimated: 3 
#> Base period: 4 
#>  
#> Balanced Panel:
#>  + No. pre-treatment periods: 4 
#>  + No. individuals: 500 
#>  + Total no. observations: 2000

The bootstrap procedures can handle unspecified equivalence thresholds:

maxEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", 
             data = sim_data, equiv_threshold = NULL, pretreatment_period = 1:4,
             base_period = 4, type = "Boot", B = 1000)
maxEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", 
             data = sim_data, equiv_threshold = NULL, pretreatment_period = 1:4,
             base_period = 4, type = "Wild", B = 1000)

The bootstrap procedures can handle unbalanced panels:

 maxEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", 
             data = unbalanced_sim_data, equiv_threshold = 1, 
             pretreatment_period = 1:4,
             base_period = 4, type = "Boot", B = 1000)
 maxEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", 
             data = unbalanced_sim_data, equiv_threshold = 1, 
             pretreatment_period = 1:4,
             base_period = 4, type = "Wild", B = 1000) 

The meanEquivTest function

The meanEquivTest implements the equivalence testing procedure surrounding the mean placebo coefficient, as described in Section 4.2.2. of Dette & Schumann (2024). The function tests the null hypothesis that the absolute mean placebo coefficient is larger than or equal to a user-specified equivalence threshold, \(\delta\). That is, if

\[\bar{\beta} = \frac{1}{T}\sum_{l=1}^{T} \beta_l,\]

the tested hypotheses can be represented as

\[H_0: |\bar{\beta}| \geq \delta \quad \text{vs.} \quad H_1: |\bar{\beta}| < \delta.\]

The null and alternative hypothesis can therefore be seen as non-negligible and negligible differences in pre-trends, respectively. Implementation of the test is similar to the maxEquivTest function in terms of the possible variance-covariance matrices (for more information on the possible variance-covariance matrices, see the documentation of the meanEquivTest function). The function returns an object of class meanEquivTest containing

One should note that rows containing NA values are removed from the panel before the testing procedure is performed.

# Perform the test with equivalent threshold specified as 1 based on 
# pre-treatment periods 1-4 and assuming homoscedastic error-terms:
  # To select variables, one can use the column names / column numbers in the panel data:
  meanEquivTest(Y = "Y", ID = "ID", G = "G", period = 2, X = c(5, 6),
                data = sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
                base_period = 4)
#> 
#>                ==================================================
#>                Equivalence Tests for Pre-trends in DiD Estimation
#>                ==================================================
#> Type: Mean Placebo Effect 
#> Alternative hypothesis: the mean placebo effect does not exceed the equivalence threshold of 1 .
#> ---
#> Abs. Mean Placebo Effect Std. Error  p-value Reject H0 
#> 0.1671                   0.09965     <2e-16  TRUE      
#> ---
#> No. placebo coefficients estimated: 3 
#> Base period: 4 
#>  
#> Balanced Panel: 
#>  + No. pre-treatment periods: 4 
#>  + No. individuals: 500 
#>  + Total no. observations: 2000
  # Alternatively, one can use separate variables:
  data_Y <- sim_data$Y
  data_ID <- sim_data$ID
  data_G <- sim_data$G
  data_period <- sim_data$period
  data_X <- sim_data[, c(5, 6)]
  meanEquivTest(Y = data_Y, ID = data_ID, G = data_G, period = data_period, X = data_X,
                equiv_threshold = 1, pretreatment_period = 1:4,
                base_period = 4)
# Perform the test with a heteroscedastic and autocorrelation robust 
# variance-covariance matrix estimator, and without specifying the equivalence threshold:
meanEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", X = c(5, 6),
              data = sim_data, equiv_threshold = NULL, pretreatment_period = 1:4,
              base_period = 4, vcov = "HAC")
#> 
#>                ==================================================
#>                Equivalence Tests for Pre-trends in DiD Estimation
#>                ==================================================
#> Type: Mean Placebo Effect 
#> Significance level: 0.05 
#> Alternative hypothesis: the mean placebo effect does not exceed the equivalence threshold.
#> ---
#> Abs. Mean Placebo Effect Std. Error  Min. Equiv. Threshold 
#> 0.1671                   0.09691     0.3265                
#> ---
#> No. placebo coefficients estimated: 3 
#> Base period: 4 
#>  
#> Balanced Panel: 
#>  + No. pre-treatment periods: 4 
#>  + No. individuals: 500 
#>  + Total no. observations: 2000
# Perform the test with an equivalence threshold of 1 and a custom
# variance-covariance matrix estimator:
vcov_func <- function(x) {plm::vcovHC(x, method = "white1", type = "HC2")}
meanEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", 
              data = sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
              base_period = 4, vcov = vcov_func)
               
# Perform the test using clustered standard errors based on a vector indicating 
# the cluster. For instance, two clusters with the following rule: all
# individuals with an ID below 250 are in the same cluster:
cluster_ind <- ifelse(sim_data$ID < 250, 1, 2)
meanEquivTest(Y = data_Y, ID = data_ID, G = data_G, period = data_period, X = data_X,
               equiv_threshold = 1, pretreatment_period = 1:4,
               base_period = 4, vcov = "CL", cluster = cluster_ind)

Note that the testing procedure can also handle unbalanced panels:

# Finally, one should note that the test procedure also works for unbalanced panels.
# To illustrate this, we generate an unbalanced panel dataset by randomly selecting
# 70% of the observations from the balanced panel dataset:
random_indices <- sample(nrow(sim_data), 0.7*nrow(sim_data))
unbalanced_sim_data <- sim_data[random_indices, ]
meanEquivTest(Y = "Y", ID = "ID", G = "G", period = "period", X = c(5, 6),
              data = unbalanced_sim_data, equiv_threshold = 1, pretreatment_period = 1:4,
              base_period = 4, vcov = "HAC")

References

Dette H., & Schumann M. (2024). “Testing for Equivalence of Pre-Trends in Difference-in-Differences Estimation.” Journal of Business & Economic Statistics, 1–13. DOI: 10.1080/07350015.2024.2308121