Simulate from the non-longitudinal pooled model.
Usage
hb_sim_pool(
n_study = 5,
n_group = 3,
n_patient = 100,
n_continuous = 0,
n_binary = 0,
s_alpha = 1,
s_delta = 1,
s_beta = 1,
s_sigma = 1,
alpha = stats::rnorm(n = 1, mean = 0, sd = s_alpha),
delta = stats::rnorm(n = n_group - 1, mean = 0, sd = s_delta),
beta = stats::rnorm(n = n_study * (n_continuous + n_binary), mean = 0, sd = s_delta),
sigma = stats::runif(n = n_study, min = 0, max = s_sigma)
)
Arguments
- n_study
Number of studies to simulate.
- n_group
Number of groups (e.g. study arms) to simulate per study.
- n_patient
Number of patients to simulate per study per group.
- n_continuous
Number of continuous covariates to simulate (all from independent standard normal distributions).
- n_binary
Number of binary covariates to simulate (all from independent Bernoulli distributions with p = 0.5).
- s_alpha
Numeric of length 1, prior standard deviation of the study-specific control group mean parameters
alpha
.- s_delta
Numeric of length 1, prior standard deviation of the study-by-group effect parameters
delta
.- s_beta
Numeric of length 1, prior standard deviation of the fixed effects
beta
.- s_sigma
Numeric of length 1, prior upper bound of the residual standard deviations.
- alpha
Numeric vector of length 1 for the pooled and mixture models and length
n_study
for the independent and hierarchical models.alpha
is the vector of control group mean parameters.alpha
enters the model by multiplying with$matrices$x_alpha
(see the return value). The control group in the data is the one with thegroup
column equal to 1.- delta
Numeric vector of length
n_group - 1
of treatment effect parameters.delta
enters the model by multiplying with$matrices$x_delta
(see the return value). The control (non-treatment) group in the data is the one with thegroup
column equal to 1.- beta
Numeric vector of
n_study * (n_continuous + n_binary)
fixed effect parameters. Within each study, the firstn_continuous
betas are for the continuous covariates, and the rest are for the binary covariates. All thebeta
s for one study appear before all thebeta
s for the next study, and studies are arranged in increasing order of the sorted unique values in$data$study
in the output.betas
enters the model by multiplying with$matrices$x_alpha
(see the return value).- sigma
Numeric vector of
n_study
study-specific residual standard deviations.
Value
A list with the following elements:
data
: tidy long-form dataset with the patient-level data. one row per patient and indicator columns for the study, group (e.g. treatment arm), and patient ID. Theresponse
columns is the patient response. The other columns are baseline covariates. The control group is the one with thegroup
column equal to 1, and the current study (non-historical) is the one with the maximum value of thestudy
column. Only the current study has any non-control-group patients, the historical studies have only the control group.parameters
: named list of model parameter values. See the model specification vignette for details.matrices
: A named list of model matrices. See the model specification vignette for details.
See also
Other simulate:
hb_sim_hierarchical()
,
hb_sim_independent()
,
hb_sim_mixture()
Examples
hb_sim_pool(n_continuous = 1)$data
#> # A tibble: 700 × 9
#> study group patient covariate_study1_continuous1 covariate_study2_continuous1
#> <int> <int> <int> <dbl> <dbl>
#> 1 1 1 1 0.749 0
#> 2 1 1 2 -0.104 0
#> 3 1 1 3 -1.78 0
#> 4 1 1 4 -0.748 0
#> 5 1 1 5 0.980 0
#> 6 1 1 6 1.92 0
#> 7 1 1 7 -0.558 0
#> 8 1 1 8 0.499 0
#> 9 1 1 9 -0.329 0
#> 10 1 1 10 -0.829 0
#> # ℹ 690 more rows
#> # ℹ 4 more variables: covariate_study3_continuous1 <dbl>,
#> # covariate_study4_continuous1 <dbl>, covariate_study5_continuous1 <dbl>,
#> # response <dbl>