\newpage
“If I had just five minutes to chop down a tree I would spend the first two and a half minutes sharpening my axe.”
— An anonymous woodsman
\vspace{13pt}
This R package provides functions for handling data from the clinical data management system (CDMS) \textcolor{blue}{secuTrial}. The most important components are related to reading data exports from secuTrial into R. In brief, the package aims to enable swift execution of repetitive tasks in order to allow spending more time on the unique aspects of a dataset. It is developed and maintained by the Swiss Clinical Trial Organisation (\textcolor{blue}{SCTO}).
If you are still challenged by more basic operations in R we suggest reading \textcolor{blue}{Hands-On Programming with R}, which serves as an excellent introduction to the basic concepts of R.
This vignette will teach you how to use the secuTrialR package and you will likely
learn quite a bit about secuTrial exports in general along the way.
Throughout the secuTrialR package and within this vignette we refer to
patients, cases, subjects etc. enrolled in a secuTrial database as participants.
Please note that R versions >= 3.5 should be used to run secuTrialR.
\vspace{5pt}
Stable release from CRAN \vspace{5pt}
install.packages("secuTrialR", dependencies = TRUE)
Development release from GitHub with devtools
For this you will need to have devtools installed.
If you are working on Windows and would like to install with devtools you
will likely need to install
\textcolor{blue}{Rtools}.
Installing everything, including the dependencies, from scratch may take a while (20-30 minutes).
\vspace{5pt}
# install
devtools::install_github("SwissClinicalTrialOrganisation/secuTrialR")
# load silently
suppressMessages(library(secuTrialR))
# show secuTrialR version
packageVersion("secuTrialR")
#> [1] '1.0.6'
Before we continue with the functionalities let's briefly talk about the test data which is
delivered as a part of the package. We refer to it as the CTU05 (clinical trial unit project 05)
data. This dataset has been fabricated for demonstration purposes only and is not
real clinical data. Principally it is made up of eight forms. These are called “surgeries”,
“baseline”, “outcome”, “treatment”, “allmedi”, “studyterminat”, “ae” and “sae”.
You will see these names again later when the data has been read into R.
The project setup includes most data types implementable in secuTrial. It is, however,
not exhaustive. Since the data is delivered with the installation of the secuTrialR
package we can point to it via the system.file() function.
\vspace{5pt}
ctu05_data_location <- system.file("extdata", "sT_exports", "exp_opt",
"s_export_CSV-xls_CTU05_all_info.zip",
package = "secuTrialR")
If you work on your own datasets you can specify a path as a regular character string without
using system.file().
Prior to reading your data into R you need to export it with the secuTrial ExportSearchTool. We suggest exporting non-rectangular, zipped, English data with reference values stored in a separate table including Add-IDs, centre information, structure information, form status, project setup, without duplicated meta data and without form data of hidden fields. Furthermore, it is important to use “CSV format”/“CSV format for MS Excel” and suggested to select UTF-8 encoding. Most of these options are truly optional and reading your data should work even with differences from the above specifications.
A description of how data can be exported from secuTrial can be found \textcolor{blue}{here}. This description includes screenshots of the export options configuration interface.
There is one principle function to read your data (i.e. read_secuTrial()).
Below you can see it in action with the CTU05 dataset.
\vspace{5pt}
ctu05_data <- read_secuTrial(data_dir = ctu05_data_location)
#> Read export successfully.
#> The following export options deviate from the suggested specifications:
#> Data from hidden fields is part of the export.
If the “Read export successfully.” message appears your data was correctly read. In this example you are also warned that hidden data fields are in the export which is a deviation from the suggested export option configuraion.
secuTrialdata objectIf you inspect the class() of ctu05_data you will find that it is a secuTrialdata object.
\vspace{5pt}
class(ctu05_data)
#> [1] "secuTrialdata"
Really this is only a list containing all the information from your secuTrial export.
\vspace{5pt}
typeof(ctu05_data)
#> [1] "list"
\newpage
secuTrialdata objectWe have implemented a custom variation of the print() function for secuTrialdata objects.
print(ctu05_data)
#> secuTrial data imported from:
#> /tmp/Rtmp3h4w8z/Rinst225b11c8d525/secuTrialR/extdata/sT_exports/exp_opt/
#> s_export_CSV-xls_CTU05_all_info.zip
#> table nrow ncol meta original_name
#> vp 4 12 TRUE vp.xls
#> vpfs 8 2 TRUE vpfs.xls
#> fs 8 8 TRUE fs.xls
#> qs 29 8 TRUE qs.xls
#> is 85 9 TRUE is.xls
#> ctr 3 3 TRUE ctr.xls
#> cn 11 15 TRUE cn.xls
#> atcn 0 9 TRUE atcn.xls
#> atcvp 0 16 TRUE atcvp.xls
#> qac 0 12 TRUE qac.xls
#> cts 0 10 TRUE cts.xls
#> miv 0 10 TRUE miv.xls
#> atmiv 0 15 FALSE atmiv.xls
#> baseline 17 107 FALSE baseline.xls
#> atbaseline 0 79 FALSE atbaseline.xls
#> outcome 13 48 FALSE outcome.xls
#> atoutcome 5 47 FALSE atoutcome.xls
#> treatment 11 44 FALSE treatment.xls
#> attreatment 0 45 FALSE attreatment.xls
#> allmedi 17 47 FALSE allmedi.xls
#> atallmedi 2 47 FALSE atallmedi.xls
#> studyterminat 10 41 FALSE studyterminat.xls
#> atstudyterminat 1 39 FALSE atstudyterminat.xls
#> ae 1 66 FALSE ae.xls
#> atae 0 58 FALSE atae.xls
#> sae 2 64 FALSE sae.xls
#> atsae 0 57 FALSE atsae.xls
#> esurgeries 18 11 FALSE esurgeries.xls
#> atesurgeries 0 9 FALSE atesurgeries.xls
#> cl 205 3 TRUE cl.xls
#> atae1 0 20 FALSE atae1.xls
It shows you where the export archive of your secuTrialdata object is located, tells you which
data tables (i.e. table) it contains, what the source files (i.e. original_name) are and
specifies each table's dimensions (i.e. ncol, nrow).
By now you have possibly realized that all the forms specified earlier (i.e. “surgeries”, “baseline”, “outcome”, “treatment”, “allmedi”, “studyterminat”, “ae” and “sae”) are present, but also that there are many tables that do not correspond to the previously introduced forms.
The majority of the unfamiliar tables are tagged as TRUE in the meta column.
This means that they are metadata tables. Their names and data structures
are fixed in secuTrial exports. In the following we will briefly explain
which information the most relevant meta tables contain.
vp - visitplan definitionvpfs - visitplan form linkagefs - forms informationqs - questionsis - items i.e. variable definitionsctr - centre informationcn - casenodes i.e. table of entered study participantscl - information how the data in the variables is codedFurthermore, there is a set of tables whose names start with “at”. These are
audit trail tables. They are only relevant if you need to investigate changes
in the data over time. For example certain values may be corrected (i.e. changed)
due to findings during monitoring visits at study centres.
Last but not least you may have also realized that the “surgeries” table is
called esurgeries. This is because it is a so-called repetition form.
Repetition forms are labelled with a leading “e” and are implemented
as subforms in other forms. In this case, esurgeries is a subform in
baseline and the linkage is defined by the mnpdocid column in both tables.
If this sounds cryptic to you we suggest you talk so someone who has implemented
a database in secuTrial and let them explain it with a specific example.
It is pretty straight forward when you look at a concrete implementation.
Since the secuTrialdata object is a list and the data tables within this list are
data.frames you can simply access the tables using $. Let's say you would like to have
a look at the placebo to verum ratio in your treatment data or what types of other
medication were entered in allmedi.
\vspace{5pt}
table(ctu05_data$treatment$rando_treatment)
#>
#> Placebo Verum
#> 8 3
table(ctu05_data$allmedi$med_product)
#>
#> Amoxicillin Doxycycline Importal
#> 2 1 3
During the loading process, coded categorical data is transformed. For example
the gender variable in the baseline form is categorical. The raw data is
accessible via gender and the transformed version of the data is added during
the reading process and becomes accessible via gender.factor. Thus, data is not overwritten
but added with the .factor extension. If there are issues during factorization
a warning() will inform you of this.
\vspace{5pt}
# raw gender data
ctu05_data$baseline$gender
#> [1] 1 NA NA 2 1 2 1 NA NA 1 2 NA NA 1 2 2 NA
#> attr(,"label")
#> [1] "Gender"
# transformed gender data
ctu05_data$baseline$gender.factor
#> [1] male <NA> <NA> female male female male <NA> <NA> male
#> [11] female <NA> <NA> male female female <NA>
#> attr(,"label")
#> [1] Gender
#> Levels: male female
# raw more meds
ctu05_data$allmedi$no_more_meds
#> [1] 1 1 0 1 1 1 0 0 0 1 0 0 1 1 1 1 0
#> attr(,"label")
#> [1] "No further medication"
# transformed more meds
ctu05_data$allmedi$no_more_meds.factor
#> [1] yes yes no yes yes yes no no no yes no no yes yes yes yes no
#> attr(,"label")
#> [1] No further medication
#> Levels: no yes
Note that descriptive labels have also been automatically added to the data. \vspace{5pt}
label(ctu05_data$allmedi$no_more_meds.factor)
#> [1] "No further medication"
label(ctu05_data$baseline$gender.factor)
#> [1] "Gender"
label(ctu05_data$esurgeries$surgery_organ.factor)
#> [1] "Organ"
Datetime data is also transformed and similarly to the factorization
process the names are concatenated with
.date or .datetime.
\vspace{5pt}
# raw
ctu05_data$baseline$visit_date
#> [1] 20190401 20190402 20190403 20190402 20190403 20190404 20190405
#> [8] 20190406 20190407 20190411 20190412 20190413 20190414 20190413
#> [15] 20190414 20190415 20180501
#> attr(,"label")
#> [1] "Date of visit"
# processed
ctu05_data$baseline$visit_date.date
#> [1] "2019-04-01" "2019-04-02" "2019-04-03" "2019-04-02" "2019-04-03"
#> [6] "2019-04-04" "2019-04-05" "2019-04-06" "2019-04-07" "2019-04-11"
#> [11] "2019-04-12" "2019-04-13" "2019-04-14" "2019-04-13" "2019-04-14"
#> [16] "2019-04-15" "2018-05-01"
# raw only head
head(ctu05_data$baseline$hiv_date)
#> [1] 201903052356 NA NA NA NA
#> [6] NA
# processed only head
head(ctu05_data$baseline$hiv_date.datetime)
#> [1] "2019-03-05 23:56:00 CET" NA
#> [3] NA NA
#> [5] NA NA
# classes
class(ctu05_data$baseline$visit_date)
#> [1] "integer"
class(ctu05_data$baseline$visit_date.date)
#> [1] "Date"
class(ctu05_data$baseline$hiv_date)
#> [1] "numeric"
class(ctu05_data$baseline$hiv_date.datetime)
#> [1] "POSIXct" "POSIXt"
Depending on the setup, incomplete dates can be valid entries in a secuTrial database.
Thus they will also occasionally appear in your exports. The datetime conversion
does not work in these cases and NAs are created. If this happens, secuTrialR will
warn you accordingly and you should have a closer look into the affected
datetime variables and whether you would like to perform so-called date imputation.
The secuTrialdata object also contains information on the export options.
\vspace{5pt}
ctu05_data$export_options
#> secuTrial version: 5.5.1.10
#> Time of export on server: 03.10.2019 - 14:43:49 (CEST)
#> Project version: (20.06.2019 - 11:22:04 (CEST))
#> Exported with short names
#> File extension: xls
#> Seperator: ' '
#> 32 files exported
#> including 13 metadata tables
#> Reference values exported - factorize possible
#> Metadata tables:
#> type exportname available
#> forms fs TRUE
#> casenodes cn TRUE
#> centres ctr TRUE
#> items is TRUE
#> questions qs TRUE
#> queries qac TRUE
#> visitplan vp TRUE
#> visitplanforms vpfs TRUE
#> atcasenodes atcn TRUE
#> atcasevisitplans atcvp TRUE
#> comments cts TRUE
#> miv miv TRUE
#> cl cl TRUE
export_options itself is a list. If you are interested in more information
than is printed you can also access it. Let's assume you would like to know
the project_name and encoding.
\vspace{5pt}
ctu05_data$export_options$project_name
#> [1] "secuTrialR example CDMA"
ctu05_data$export_options$encoding
#> [1] "UTF-8"
Much more information is stored in the elements of export_options.
The names of the elements should be descriptive enough to infer the contents.
\vspace{5pt}
names(ctu05_data$export_options)
#> [1] "sep" "date_format" "datetime_format"
#> [4] "date_format_meta" "na.strings" "short_names"
#> [7] "is_zip" "is_rectangular" "audit_trail"
#> [10] "column_names" "lang_not_supported" "dict_items"
#> [13] "refvals_separate" "add_id" "lab_id"
#> [16] "meta_names" "meta_available" "duplicate_meta"
#> [19] "all_files" "data_files" "data_names"
#> [22] "file_end" "extension" "data_dir"
#> [25] "secuTrial_version" "project_version" "project_name"
#> [28] "format_info" "time_of_export" "encoding"
#> [31] "form_status" "centre_info" "hidden_fields"
#> [34] "structure" "proj_setup" "factorized"
#> [37] "dated" "labelled"
secuTrialdata objectsNow that you understand the secuTrialdata object we will show you some generic functions
you can use on objects of this class.
First off you may be interested in a table of participants. \vspace{5pt}
get_participants(ctu05_data)
#> mnppid mnpaid mnpctrid mnpctrname
#> 1 1204 RPACK-CBE-001 462 Charité Berlin (RPACK)
#> 2 1205 RPACK-CBE-002 462 Charité Berlin (RPACK)
#> 3 1206 RPACK-CBE-003 462 Charité Berlin (RPACK)
#> 4 1207 RPACK-CBE-004 462 Charité Berlin (RPACK)
#> 5 1208 RPACK-CBE-005 462 Charité Berlin (RPACK)
#> 6 1209 RPACK-INS-011 461 Inselspital Bern (RPACK)
#> 7 1210 RPACK-INS-012 461 Inselspital Bern (RPACK)
#> 8 1211 RPACK-INS-013 461 Inselspital Bern (RPACK)
#> 9 1212 RPACK-INS-014 461 Inselspital Bern (RPACK)
#> 10 1213 RPACK-INS-015 461 Inselspital Bern (RPACK)
#> 11 1214 RPACK-USB-123 441 Universitätsspital Basel (RPACK)
Please note that the mnpaid column in this table corresponds to the pat_id
column in other tables.
\newpage
You can extract information about participant recruitment per centre and year by applying
annual_recruitment() on a secuTrialdata object.
\vspace{5pt}
annual_recruitment(ctu05_data)
#> Center Total 2018 2019
#> 1 All 11 1 10
#> 2 Charité Berlin (RPACK) 5 0 5
#> 3 Inselspital Bern (RPACK) 5 0 5
#> 4 Universitätsspital Basel (RPACK) 1 1 0
Since the centre names often have a systematic addition (e.g. (RPACK)) we have
enabled the option to remove certain parts of the centre descriptions via
regular expressions (i.e. rm_regex argument). In this case the regular expression
removes trailing parentheses and everything they enclose.
\vspace{5pt}
annual_recruitment(ctu05_data, rm_regex = "\\(.*\\)$")
#> Center Total 2018 2019
#> 1 All 11 1 10
#> 2 Charité Berlin 5 0 5
#> 3 Inselspital Bern 5 0 5
#> 4 Universitätsspital Basel 1 1 0
It is also possible to plot the recruitment over time. \vspace{5pt}
plot_recruitment(ctu05_data, cex = 1.2, rm_regex = "\\(.*\\)$")
\newpage
secuTrialR can provide a depiction of the visit structure, although only where
the visit plan is fixed. Black rectangles in the grid represent a form to be filled (x)
during one of the visits (y).
\vspace{5pt}
vs <- visit_structure(ctu05_data)
plot(vs)
If you are not sure about how complete the data in your export is, it may be useful to get a quick overview of how well the forms have been filled. The below table shows both absolute and relative numbers for a few forms. \vspace{5pt}
fss <- form_status_summary(ctu05_data)
tail(fss, n = 5)
#> form_name partly_filled completely_filled empty with_warnings
#> 6 baseline 3 14 0 0
#> 7 outcome 1 12 0 0
#> 8 sae 0 2 0 0
#> 9 studyterminat 0 10 0 0
#> 10 treatment 0 11 0 0
#> with_errors partly_filled.percent completely_filled.percent
#> 6 0 0.17647059 0.8235294
#> 7 0 0.07692308 0.9230769
#> 8 0 0.00000000 1.0000000
#> 9 0 0.00000000 1.0000000
#> 10 0 0.00000000 1.0000000
#> empty.percent with_warnings.percent with_errors.percent form_count
#> 6 0 0 0 17
#> 7 0 0 0 13
#> 8 0 0 0 2
#> 9 0 0 0 10
#> 10 0 0 0 11
Please note that a form is only complete if all required fields have been filled. Thus, a whole study may have 99% completeness on variable basis while showing 0% completeness on form basis. It is currently not technically possible to assess completeness on variable basis in a generic way. Hence, high completeness on form basis implies high completeness on variable basis but NOT vice versa.
If you would rather retrieve information on form completeness for each participant individually you can perform the following. \vspace{5pt}
fsc <- form_status_counts(ctu05_data)
# show the top
head(fsc)
#> pat_id form_name completely_filled partly_filled empty
#> 1 RPACK-CBE-001 baseline 3 0 0
#> 2 RPACK-CBE-002 baseline 1 0 0
#> 3 RPACK-CBE-003 baseline 1 0 0
#> 4 RPACK-CBE-004 baseline 1 0 0
#> 5 RPACK-CBE-005 baseline 1 2 0
#> 6 RPACK-INS-011 baseline 1 0 0
#> with_warnings with_errors
#> 1 0 0
#> 2 0 0
#> 3 0 0
#> 4 0 0
#> 5 0 0
#> 6 0 0
Linkages amongst forms can be explored with the links_secuTrial() function.
This relies on the igraph package to create a network. It is possible to
interact with the network, e.g. move nodes around in order to read the labels better.
The R graphics device ID is returned to the console, but can be ignored. Forms are plotted in
deep yellow, variables in light blue.
\vspace{5pt}
links_secuTrial(ctu05_data)
The output can not be shown within this vignette but you should give it a try. Please note that the linkage plot is likely most useful without the audit trail data in the export.
\newpage
During study monitoring it is common practice to check random participants from a study database. These participants should be retrieved in a reproducible fashion, which can be achieved by setting a so-called seed. The below function allows reproducible retrieval for a loaded secuTrial data export. \vspace{5pt}
# randomly retrieve at least 25 percent of participants recorded after March 18th 2019
# from the centres "Inselspital Bern" and "Charité Berlin"
return_random_participants(ctu05_data,
percent = 0.25,
seed = 1337,
date = "2019-03-18",
centres = c("Inselspital Bern (RPACK)",
"Charité Berlin (RPACK)"))
#> $participants
#> mnpaid centre mnpvisstartdate
#> 2 RPACK-INS-012 Inselspital Bern (RPACK) 2019-04-12
#> 4 RPACK-INS-014 Inselspital Bern (RPACK) 2019-04-14
#> 5 RPACK-CBE-005 Charité Berlin (RPACK) 2019-04-05
#> 3 RPACK-CBE-003 Charité Berlin (RPACK) 2019-04-03
#>
#> $rng_config
#> [1] "Mersenne-Twister" "Inversion" "Rejection"
Please note that earlier R versions may return different results because
there is a different rng_config (i.e. RNGkind()).
For this reason we have added the rng_config to the output.
secuTrial allows implementing calculated variables (i.e. scores). Data is not directly entered into these variables but rather calculated automatically. Scores are defined by a set of rules and use the data in other variables as basis. For example the age of a study participant at data entry can be calculated as the difference between the participant's birthday and the day of data entry.
It is advisable to recalculate or validate score variable data before data analysis. A rule of thumb: The more complex a score is and the more data from different forms is necessary for its calculation the more likely its value should be recalculated. The below function will allow you to detect which variables this concerns. \vspace{5pt}
return_scores(ctu05_data)
#> name itemtype label
#> 1 age Years y (calculated only) Age
Sometimes, during a study, certain fields may be hidden because data should no longer be entered into them. If this is the case and the data of these fields is part of your export is likely good to know about it. In this case nothing is hidden. \vspace{5pt}
return_hidden_items(ctu05_data)
#> [1] name itemtype label
#> <0 rows> (or 0-length row.names)
In ongoing studies it is possible that changes to the secuTrial data entry
interface (i.e. the electronic case report forms) are made. Sometimes these
changes may call for adjustments in analysis code. It is considered good practice
to run diff_secuTrial() on the last export and the current export of a project
to at least make yourself aware of potential changes in the setup. If there are
differences, the results of this function should be interpreted as a first indicator
since they may not cover all alterations. Information is returned on forms and
variables. A detailed list of changes can be produced in the secuTrial
FormBuilder with “Compare project setup”.
For the below diff_secuTrial() showcase we emulated a changed setup of CTU05
by copying the setup and importing it in the FormBuilder as a new secuTrial
project (CTU06). From this, we created a data export (v1) and then made a few
minor changes and exported again (v2). If this sounds confusing, never mind.
CTU06 v1 is simply a copy of CTU05. CTU06 v2 is a slighly altered version of CTU06 v1.
\vspace{5pt}
ctu06_v1 <- read_secuTrial(system.file("extdata", "sT_exports", "change_tracking",
"s_export_CSV-xls_CTU06_version1.zip",
package = "secuTrialR"))
#> Read export successfully.
#> The following export options deviate from the suggested specifications:
#> Data from hidden fields is part of the export.
ctu06_v2 <- read_secuTrial(system.file("extdata", "sT_exports", "change_tracking",
"s_export_CSV-xls_CTU06_version2.zip",
package = "secuTrialR"))
#> Read export successfully.
#> The following export options deviate from the suggested specifications:
#> Data from hidden fields is part of the export.
diff_secuTrial(ctu06_v1, ctu06_v2)
#> $new_forms
#> [1] "mnpctu06anewform" "mnpctu06anothernewform"
#>
#> $new_variables
#> [1] "new_item_in_fu" "new_item_in_new_form"
#>
#> $removed_forms
#> character(0)
#>
#> $removed_variables
#> character(0)
As you can see ctu06_v2 contains the two additional forms mnpctu06anewform and
mnpctu06anothernewform and the two additional variables new_item_in_fu and
new_item_in_new_form.
Given that you are working with R it is unlikely that you need such conversions for
yourself. However, collaborators may ask for data which is readily importable into SPSS,
STATA or SAS. For this you can use write_secuTrial().
Since this has not been heavily tested or used there may be issues and
you might prefer doing this manually with the haven package. One particular
sticking point is the length of variable names - R is not restrictive in this
respect, but other software can be. secuTrialR does not truncate names, prefering
to leave this to the user, which can cause write_secuTrial() to fail with an error.
\vspace{5pt}
# retrieve path to a temporary directory
tdir <- tempdir()
# write spss
write_secuTrial(ctu05_data, format = "sav", path = tdir)
secuTrialdataIn some cases it may be useful to subset your secuTrialdata object.
For example if you have cohort data and would like to supply a subset of
the data for a retrospective study. We have implemented this
option with subset_secuTrial(). It will truncate your secuTrialdata object
and return a new secuTrialdata object which is a subset of the original data.
It is possible to subset by including or excluding specific participant
ids or centres.
\vspace{5pt}
# initialize some subset identifiers
participants <- c("RPACK-INS-011", "RPACK-INS-014", "RPACK-INS-015")
centres <- c("Inselspital Bern (RPACK)", "Universitätsspital Basel (RPACK)")
# exclude Bern and Basel
ctu05_data_berlin <- subset_secuTrial(ctu05_data, centre = centres, exclude = TRUE)
#> If you changed any labels in the secuTrialdata object manually these will be reset to their original state.
# exclude Berlin
ctu05_data_bern_basel <- subset_secuTrial(ctu05_data, centre = centres)
#> If you changed any labels in the secuTrialdata object manually these will be reset to their original state.
# keep only subset of participants
ctu05_data_pids <- subset_secuTrial(ctu05_data, participant = participants)
#> If you changed any labels in the secuTrialdata object manually these will be reset to their original state.
class(ctu05_data_berlin)
#> [1] "secuTrialdata"
class(ctu05_data_bern_basel)
#> [1] "secuTrialdata"
class(ctu05_data_pids)
#> [1] "secuTrialdata"
If you subset based on centres all traces of deleted centres will be removed. If you remove based on participant ids all traces of deleted participants will be removed. \vspace{5pt}
# only Berlin remains
ctu05_data_berlin$ctr
#> mnpctrid mnpctrname mnpcname
#> 1 462 Charité Berlin (RPACK) NA
# all centres remain even though all three participant ids are from Bern
ctu05_data_pids$ctr
#> mnpctrid mnpctrname mnpcname
#> 1 462 Charité Berlin (RPACK) NA
#> 2 461 Inselspital Bern (RPACK) NA
#> 3 441 Universitätsspital Basel (RPACK) NA
\newpage
Since the truncated object's class remains unchanged (i.e. secuTrialdata) you can
still use the generic functions on it.
Let's say you would only like to look at the recruitment plot for Bern alone.
\vspace{5pt}
# keep only Bern
ctu05_data_bern <- subset_secuTrial(ctu05_data, centre = "Inselspital Bern (RPACK)")
#> If you changed any labels in the secuTrialdata object manually these will be reset to their original state.
# plot
plot_recruitment(ctu05_data_bern)
… or Bern and Berlin. \vspace{5pt}
# keep only Bern and Berlin
ctu05_data_bern_berlin <- subset_secuTrial(ctu05_data,
centre = c("Inselspital Bern (RPACK)",
"Charité Berlin (RPACK)"))
#> If you changed any labels in the secuTrialdata object manually these will be reset to their original state.
# plot
plot_recruitment(ctu05_data_bern_berlin)
If you are creating reports in which you would like to directly
link to specific pages of your secuTrial DataCapture you can
use build_secuTrial_url. If you are no expert regarding the
secuTrial server architecture you would like to build links for, you should
talk to the server admin or consult the build_secuTrial_url help page.
They will be able to guide you regarding the information for the server,
instance, customer and project parameters. The docid, however, is
included in your export data in the non-meta data tables of the
secuTrialdata object and can be found in the mnpdocid columns.
head(ctu05_data$treatment$mnpdocid)
#> [1] 181 193 200 205 213 224
head(ctu05_data$baseline$mnpdocid)
#> [1] 180 184 187 191 199 203
To demsonstrate build_secuTrial_url we will use imaginary data
for the server, instance, customer and project parameters.
The real counterparts on your server will likely look structurally
similar.
server <- "server.secutrial.com"
instance <- "ST21-setup-DataCapture"
customer <- "TES"
project <- "7036"
# make three links with the first three baseline docids
bl_docids <- head(ctu05_data$baseline$mnpdocid, n = 3)
links <- build_secuTrial_url(server, instance, customer,
project, bl_docids)
These are the links:
https://server.secutrial.com/apps/WebObjects/ST21-setup-DataCapture.woa/wa/choose?customer=TES&projectid=7036&docid=180
Of course they are dead ends but maybe you can use them to make out the arguments for your server.
as.data.frame functionThis vignette has been working with the secuTrialdata object, which is of type list.
For some users, working with a list can be tiresome so secuTrialR provides an
as.data.frame() method to save the data.frames in the secuTrialdata object to
an environment of your choice.
As an example, we will create an environment called env and check that it's empty
before running as.data.frame()…
\vspace{5pt}
env <- new.env()
ls(env)
#> character(0)
# add files to env
as.data.frame(ctu05_data, envir = env)
… and afterwards. \vspace{5pt}
ls(env)
#> [1] "ae" "allmedi" "atae"
#> [4] "atae1" "atallmedi" "atbaseline"
#> [7] "atesurgeries" "atmiv" "atoutcome"
#> [10] "atsae" "atstudyterminat" "attreatment"
#> [13] "baseline" "esurgeries" "outcome"
#> [16] "sae" "studyterminat" "treatment"
Substituting env with .GlobalEnv instead would also be an option and would make the data.frames immediately accessible without having to refer to an environment.
Certain warning messages can occur quite frequently when running read_secuTrial().
Some of them may call for deliberate action and thus it is important to understand them.
We briefly mentioned some of them earlier in this document but will now more closely
explain how they can be interpreted.
Please note that warning messages may “pile up” depending on the export you are reading.
For example this may happen if there are many date variables with incomplete data. This is
no reason for concern. We suggest that you read them and interpret them based on the
explanations below. We use a_form_name and a_variable_name as place holders in the examples.
If in doubt you can always work with the raw data because it is never overwritten.
The below warning tells you that some data in a date variable could not be converted
during the process of date conversion (i.e. dates_secuTrial()). This ususally occurs
if incomplete date entries are present. Since the raw data is not overwritten but rather a
variable_name.date or variable_name.datetime column are added to the dataset you can specifically see which
values could not be converted because the raw data will contain data while the corresponding .date/.datetime
entires will be NA. The warning also indicates where to look. The dummy example below indicates to look
at the variable a_variable_name in form a_form_name.
#> Warning: In dates_secuTrial.data.frame(tmp, datevars, timevars, dateformat, :
#> Not all dates were converted for
#> variable: 'a_variable_name'
#> in form: 'a_form_name'
#> This is likely due to incomplete date entries.
In some cases secuTrial allows differently coded data to be decoded to the same target value for the
same variable. For instance this can happen if hierarchical lookuptables have been implemented
in the database. Because this interferes with the factorization (i.e. factorize_secuTrial())
we add the code to the duplicate decoded value and return the below message to make you aware.
If you run into this warning message we suggest running the table() function on the
variable in question. This will likely clarify the above explanation.
#> Warning: In factorize_secuTrial.data.frame(curr_form_data, cl = object$cl, :
#> Duplicate values found during factorization of a_variable_name
Sometimes the labels of variables in a secuTrial database implementation may be changed
after release of the database. In these cases all labels (current and previous versions) are
added to the label attribute during labelling (i.e. label_secuTrial()) and the below warning
is triggered. It indicates which variables in which forms are affected.
#> Warning: In label_secuTrial.secuTrialdata(d) :
#> The labels attribute may be longer than 1 for the following variables and forms.
#> Likely the label was changed from its original state in the secuTrial project setup.
#> variables: a_variable_name
#> forms: a_form_name
secuTrialdata objectNaturally, you will sometimes need to merge/join some of the data from the individual form data stored
in your secuTrialdata object. To achieve this you can use the base R merge() function.
For our dataset we might be interested in merging the baseline form data with that of the treatment
form. For this we can use the mnpcvpid which uniquely identifies each participant visit. Since we
are only interested in the rando_treatment variable we will shrink the data in the treatment form prior to merging.
\vspace{5pt}
treatment_shrink <- ctu05_data$treatment[, c("mnpcvpid", "rando_treatment")]
Because we do not want to drop non-matching rows from baseline we set all.x = TRUE.
As you can see from the dim() calls, one column has been added after the merge.
This corresponds to the rando_treatment variable.
bl_treat <- merge(x = ctu05_data$baseline, y = treatment_shrink,
by = "mnpcvpid", all.x = TRUE)
# check dimensions
dim(ctu05_data$baseline)
#> [1] 17 107
dim(bl_treat)
#> [1] 17 108
Another common task may be to merge repetition form data to its parent form.
In our case esurgeries can be naively merged with baseline via the
mnpdocid (from the secuTrial manual: “Each eCRF document record has a unique document identifier.”):
\vspace{5pt}
bl_surg <- merge(x = ctu05_data$baseline, y = ctu05_data$esurgeries, by = "mnpdocid")
Please note, that such naive merging can cause duplication of data if the ids that the merge is directed by are not unique.
This also happened during the production of bl_surg in the code above. Participant “RPACK-INS-012” exhibits the
mnpdocid 234 twice in the esurgeries repetition form which causes a duplication of the baseline data matching
mnpdocid 234.
\vspace{5pt}
table(ctu05_data$esurgeries$mnpdocid)
#>
#> 180 184 187 191 199 203 211 216 220 222 230 234 238 243 249 255 265
#> 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 1 1
Lets briefly illustrate the consequences by looking at a table() of the height variable from the baseline
form before and after merging.
\vspace{5pt}
# before merge
table(ctu05_data$baseline$height)
#>
#> 110.1 150 150.1 160 167.9 170.3 170.4 180 180.1 190.2
#> 1 1 1 1 1 1 1 3 3 1
# after merge
table(bl_surg$height)
#>
#> 110.1 150 150.1 160 167.9 170.3 170.4 180 180.1 190.2
#> 1 1 1 1 1 1 1 4 3 1
A closer look reveals that 180 now appears four times instead of three, which can be attributed to
the duplication. This is not a favourable outcome because it can cause confusion and misinterpretation.
A better approach is to change the structure of your repetition form before merging to make the ids you merge by unique.
For this you need to investigate which data you would like to merge and design an appropriate stategy.
In our example case we are interested in the surgery_organ. Of course we also need to drag the mnpdocid along
to perform the actual merge.
\vspace{5pt}
# write a temporary object
surg <- ctu05_data$esurgeries[, c("mnpdocid", "surgery_organ.factor")]
# only retain non NA rows
surg <- surg[which(! is.na(surg$surgery_organ.factor)), ]
# show it
surg
#> mnpdocid surgery_organ.factor
#> 12 234 Stomach
#> 13 234 Other
\newpage
In order to prevent duplication we can restructure the data before merging.
\vspace{5pt}
library(tidyr) # pivot_wider
# add a count
surg$count <- 1
# show the data
surg
#> mnpdocid surgery_organ.factor count
#> 12 234 Stomach 1
#> 13 234 Other 1
# make it wide
surg_wide <- pivot_wider(surg, names_from = surgery_organ.factor, values_from = count)
# show the wide data
surg_wide
#> # A tibble: 1 x 3
#> mnpdocid Stomach Other
#> <int> <dbl> <dbl>
#> 1 234 1 1
Checking the dimensions before and after merging reveals that the structure, especially the line count, remains
the same except for the data added from the esurgeries repetition form (i.e. Stomach and Other). Also,
as expected, the table() of the height variable returns the expected result (i.e. 180 is present three not four times).
\vspace{5pt}
# merge
bl_surg_no_dup <- merge(x = ctu05_data$baseline, y = surg_wide,
by = "mnpdocid", all.x = TRUE)
# compare dimensions
dim(bl_surg_no_dup)
#> [1] 17 109
dim(ctu05_data$baseline)
#> [1] 17 107
# check the height variable
table(bl_surg_no_dup$height)
#>
#> 110.1 150 150.1 160 167.9 170.3 170.4 180 180.1 190.2
#> 1 1 1 1 1 1 1 3 3 1
The above description only provides a very brief and simplified example. Merging
strategies need to be individually tailored and require a good understanding of the data at hand.
The links_secuTrial() function may be helpful to understand which variables will allow you to
merge forms.
mnp* variablesThere is a plethora of variables in the tables of secuTrial exports whose names start
with mnp. These are metadata variables which are e.g. important to logically link the
different tables. Explaining them all is beyond the scope of this vignette.
For detailed explanations, please refer to the secuTrial “Export Formats” user manual.
\newpage
sessionInfo()
#> R version 3.6.3 (2020-02-29)
#> Platform: x86_64-pc-linux-gnu (64-bit)
#> Running under: Ubuntu 18.04.5 LTS
#>
#> Matrix products: default
#> BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.7.1
#> LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.7.1
#>
#> locale:
#> [1] LC_CTYPE=C.UTF-8 LC_NUMERIC=C LC_TIME=C.UTF-8
#> [4] LC_COLLATE=C LC_MONETARY=C.UTF-8 LC_MESSAGES=C.UTF-8
#> [7] LC_PAPER=C.UTF-8 LC_NAME=C LC_ADDRESS=C
#> [10] LC_TELEPHONE=C LC_MEASUREMENT=C.UTF-8 LC_IDENTIFICATION=C
#>
#> attached base packages:
#> [1] stats graphics grDevices utils datasets methods base
#>
#> other attached packages:
#> [1] tidyr_1.0.0 secuTrialR_1.0.6
#>
#> loaded via a namespace (and not attached):
#> [1] igraph_1.2.4.1 Rcpp_1.0.3 knitr_1.25 magrittr_1.5
#> [5] hms_0.5.2 tidyselect_1.1.0 R6_2.4.0 rlang_0.4.6
#> [9] fansi_0.4.0 highr_0.8 stringr_1.4.0 dplyr_1.0.0
#> [13] tcltk_3.6.3 tools_3.6.3 xfun_0.10 utf8_1.1.4
#> [17] cli_1.1.0 htmltools_0.4.0 assertthat_0.2.1 readxl_1.3.1
#> [21] digest_0.6.22 tibble_2.1.3 lifecycle_0.2.0 crayon_1.3.4
#> [25] purrr_0.3.3 readr_1.3.1 vctrs_0.3.1 glue_1.4.1
#> [29] evaluate_0.14 haven_2.3.1 stringi_1.4.3 cellranger_1.1.0
#> [33] compiler_3.6.3 pillar_1.4.2 forcats_0.4.0 generics_0.0.2
#> [37] lubridate_1.7.4 tufte_0.5 pkgconfig_2.0.3
\vspace{185pt}
Disclaimer
The descriptions of the secuTrial exports used in this vignette and other secuTrialR
documentation correspond to our understanding of them and come with no warranty.
For in depth details please refer to the original secuTrial manuals.