Type: | Package |
Title: | A Toolbox for Clinical Significance Analyses in Intervention Studies |
Version: | 2.1.0 |
Description: | A clinical significance analysis can be used to determine if an intervention has a meaningful or practical effect for patients. You provide a tidy data set plus a few more metrics and this package will take care of it to make your results publication ready. Accompanying package to Claus et al. <doi:10.18637/jss.v111.i01>. |
License: | GPL (≥ 3) |
Encoding: | UTF-8 |
LazyData: | true |
Depends: | R (≥ 2.10) |
RoxygenNote: | 7.3.2 |
Imports: | BayesFactor, bayestestR, cli, dplyr, ggplot2, insight, lme4, purrr, rlang, tibble, tidyr |
Suggests: | knitr, rmarkdown, testthat (≥ 3.0.0), tidyverse, vdiffr |
Config/testthat/edition: | 3 |
VignetteBuilder: | knitr |
URL: | https://pedscience.github.io/clinicalsignificance/, https://github.com/pedscience/clinicalsignificance |
BugReports: | https://github.com/pedscience/clinicalsignificance/issues |
NeedsCompilation: | no |
Packaged: | 2024-12-02 14:58:09 UTC; bened |
Author: | Benedikt Claus |
Maintainer: | Benedikt Claus <b.claus@pedscience.de> |
Repository: | CRAN |
Date/Publication: | 2024-12-02 15:40:16 UTC |
Antidepressant Data
Description
A fictional dataset used to showcase group-based clinical significance analyses and analyses with many participants.
Usage
antidepressants
Format
A tibble with 1140 rows and 4 variables:
patient
Patient identifier
condition
Experimental condition
measurement
Indicator of measurement
mom_di
Mind over Mood Depression inventory scores (lower is better)
Details
In a fictional clinical trial, the effectiveness of a new antidepressant should be examined and depressed patients were randomized to one of four groups:
A wait list control group that did not receive a medication
An inactive placebo group, i.e., a group that received a placebo (inert substance without proposed clinical effect) pill
An active placebo group, i.e., a group that received a placebo that evokes side effects like mild nausea or a dry mouth
The antidepressant group, so the target medication of this trial that should have a clinical impact on the patients' depressive symptoms
Suppose they underwent outpatient treatment, depressive symptoms were measured before and after treatment with the Mind over Mood Depression Inventory (MoM-DI) by Greenberger & Padesky (2015), and if a patient received a pill, the clinician and the patient did not know, what type of medicaction they consumed.
Further, the minimal important difference for an improvement as measured by this instrument was agreed to be an 8 point decrease. A deterioration can be assumed if instrument scores increased by 5 points.
The functional population (i.e., non-depressed individuals) can be expected to have a mean score of M = 8 points with a standard deviation of SD = 7.
References
Greenberger, D., & Padesky, C. A. (2015). Mind over mood, second edition (2nd ed.). New York, NY: Guilford Publications.
Anxiety Data
Description
A fictional dataset with missings to exemplify the use of HLM method for clinical significance.
Usage
anxiety
Format
A data frame with 580 rows and 4 variables:
subject
Participant
treatment
Treatment. Either Placebo or Intervention
measurement
Number of measurement
anxiety
Anxiety score (lower is better)
Details
In a fictional clinical trial, participants were split up to belong to either a medical placebo ("Placebo") or psychotherapeutic intervention ("Intervention") group.
They underwent outpatient treatment during which they were followed for 5 measurements at which a fictional anxiety score was measured. This anxiety score may range from 0 - 60.
The functional population (i.e., non-anxious individuals) can be expected to have a mean score of M = 8 points with a standard deviation of SD = 4.
Anxiety Data (Complete)
Description
A fictional complete dataset to exemplify the use of HLM method for clinical significance.
Usage
anxiety_complete
Format
A data frame with 580 rows and 4 variables:
subject
Participant
treatment
Treatment. Either Placebo or Intervention
measurement
Number of measurement
anxiety
Anxiety score (lower is better)
Details
In a fictional clinical trial, participants were split up to belong to either a medical placebo ("Placebo") or psychotherapeutic intervention ("Intervention") group.
They underwent outpatient treatment during which they were followed for 5 measurements at which a fictional anxiety score was measured. This anxiety score may range from 0 - 60.
The functional population (i.e., non-anxious individuals) can be expected to have a mean score of M = 8 points with a standard deviation of SD = 4.
Generic to Calculate Anchor-Based Results
Description
This is an internal generic and should not be called directly. Depending on the different anchor method requested by the user, the appropriate method is called. It calculates the change and according clinical significance category for each participant.
Usage
calc_anchor(data, ...)
Arguments
data |
A data set object of class |
... |
Additional arguments |
Value
An object of class cs_anchor_*
Anchor Calculations for Group Effect Between
Description
Anchor Calculations for Group Effect Between
Usage
## S3 method for class 'cs_anchor_group_between'
calc_anchor(
data,
mid_improvement,
mid_deterioration,
reference_group,
post,
direction,
ci_level,
bayesian,
prior_scale,
...
)
Arguments
reference_group |
String, the reference group to compare all other groups against |
post |
The measurement at which groups should be compared, typically a measurement after an intervention. |
Anchor Calculations for Group Effect Within
Description
This is an internal function and should never be called directly.
Usage
## S3 method for class 'cs_anchor_group_within'
calc_anchor(
data,
mid_improvement,
mid_deterioration,
direction,
ci_level,
bayesian,
prior_scale,
...
)
Arguments
bayesian |
Logical, if Bayesian tests and uncertainty intervals should
be used, defaults to |
prior_scale |
String or numeric, can be adjusted to change the Bayesian
prior distribution. See the documentation for |
Anchor Calculations for Individual Results
Description
Anchor Calculations for Individual Results
Usage
## S3 method for class 'cs_anchor_individual_within'
calc_anchor(data, mid_improvement, mid_deterioration, direction, ci_level, ...)
Arguments
mid_improvement |
Numeric, change that indicates a clinically significant improvement |
mid_deterioration |
Numeric, change that indicates a clinically significant deterioration |
direction |
Which direction is beneficial? Lower = -1, better = 1 |
ci_level |
Numeric, desired confidence interval. |
Generic for Statistical Approach
Description
This is an internal generic and should not be called directly. Depending on the different cutoff method requested by the user, the appropriate method is called. It calculates the cutoff and according clinical significance category for each participant.
Usage
calc_cutoff_from_data(data, ...)
Arguments
data |
A pre-processed wide data frame with at least column |
... |
Additional arguments for the respective cutoff method |
Value
A list with cutoff info and participant wise info on cutoff categorization
Calculate cs_indiv
Description
Calculate cs_indiv
Usage
## S3 method for class 'cs_ha'
calc_cutoff_from_data(
data,
m_clinical,
sd_clinical,
m_functional,
sd_functional,
m_post,
sd_post,
reliability,
type = "a",
direction = 1,
critical_value = 1.65,
...
)
Arguments
m_clinical |
Mean of clinical population |
sd_clinical |
SD of clinical population |
m_post |
Mean of post measurement |
sd_post |
SD of post measurement |
reliability |
Instrument's reliability |
critical_value |
The critical value for the RCI decision, should be 1.65 if significance_level = 0.05 |
Calculate the categories based on the cutoff
Description
Calculate the categories based on the cutoff
Usage
## Default S3 method:
calc_cutoff_from_data(
data,
m_clinical,
sd_clinical,
m_functional,
sd_functional,
type = "a",
direction = 1,
...
)
Arguments
data |
Prepped data with class |
m_functional |
Mean of functional population |
sd_functional |
SD of functional population |
type |
Cutoff type, available are |
... |
Additional arguments for the specific RCI method |
Calculate Change for the Percentage-Change Approach
Description
This is an internal generic and should not be called directly. Depending on the different percent change cutoff requested by the user, this function calculates the relative change according clinical significance category for each patient.
Usage
calc_percentage(data, pct_improvement, pct_deterioration, direction)
Arguments
data |
A pre-processed data frame with at least columns |
pct_improvement |
Numeric, the required percent change cutoff to infer an improvement |
pct_deterioration |
Numeric, the required percent change cutoff to infer a deterioration |
Value
An object of classm cs_percentage
list with participant-wise info
on clinical significant change catergory
Generic to Calculate RCI and Associated Change
Description
This is an internal generic and should not be called directly. Depending on the different RCI method requested by the user, the appropriate method is called. It calculates the RCI and according clinical significance category for each participant.
Usage
calc_rci(data, ...)
Arguments
data |
Prepped data with class |
... |
Additional arguments for the specific RCI method |
Value
RCI result object with class cs_distribution
RCI for the Edwards method
Description
RCI for the Edwards method
Usage
## S3 method for class 'cs_en'
calc_rci(
data,
m_pre,
sd_pre,
reliability,
direction = 1,
critical_value = 1.96,
...
)
RCI for the Gulliksen, Lord & Novick method
Description
RCI for the Gulliksen, Lord & Novick method
Usage
## S3 method for class 'cs_gln'
calc_rci(
data,
m_pre,
sd_pre,
reliability,
direction = 1,
critical_value = 1.96,
...
)
Arguments
m_pre |
Pre measurement mean |
RCI for the Hageman & Arrindell
Description
RCI for the Hageman & Arrindell
Usage
## S3 method for class 'cs_ha'
calc_rci(
data,
m_pre,
sd_pre,
m_post,
sd_post,
reliability,
direction = 1,
critical_value = 1.65,
...
)
Arguments
sd_post |
Post measurement SD |
RCI for the Hsu, Lin & Lord method
Description
RCI for the Hsu, Lin & Lord method
Usage
## S3 method for class 'cs_hll'
calc_rci(
data,
m_pre,
sd_pre,
m_post,
reliability,
direction = 1,
critical_value = 1.96,
...
)
Arguments
m_post |
Post measurement mean |
Calc RCI for the HLM method
Description
Calc RCI for the HLM method
Usage
## S3 method for class 'cs_hlm'
calc_rci(data, direction, critical_value = 1.96, ...)
RCI for the Jacobson & Truax method
Description
RCI for the Jacobson & Truax method
Usage
## S3 method for class 'cs_jt'
calc_rci(data, sd_pre, reliability, direction = 1, critical_value = 1.96, ...)
Arguments
sd_pre |
Pre measurement SD |
reliability |
Instrument reliability |
direction |
Beneficial intervention effect for given instrument. 1 = higher is better, -1 = lower is better |
critical_value |
Critical RCI value, typically 1.96 |
RCI for the NK method
Description
RCI for the NK method
Usage
## S3 method for class 'cs_nk'
calc_rci(
data,
m_pre,
sd_pre,
reliability,
reliability_post,
direction = 1,
critical_value = 1.96,
...
)
Arguments
reliability_post |
Instrument reliability at post measurement |
Placebo Amplification Data
Description
A dataset containing the data from Claus et al. (2020). In a routine inpatient setting for unipolar depressive disorders they implemented an intervention that sought to amplify the placebo response of antidepressants. In the study, two groups were compared: treatment as usual (TAU) and placebo amplification (PA). Participants were examined four times during their treatment.
Usage
claus_2020
Format
An object of class tbl_df
with 172 rows and 9 columns.
- id
Participant ID
- age
Age
- sex
Sex
- treatment
Treatment (TAU for treatment as usual and PA for placebo amplification)
- time
Measurement
- bdi
Beck Depression Inventory (2nd Edition) score (lower is better)
- shaps
Snaith-Hamilton Pleasure Scale score (higher is better)
- who
WHO-Five Well-Being Index score (higher is better)
- hamd
Hamilton Rating Scale for Depression score (lower is better)
Source
References
Claus, B. B., Scherbaum, N., & Bonnet, U. (2020). Effectiveness of an Adjunctive Psychotherapeutic Intervention Developed for Enhancing the Placebo Effect of Antidepressants Used within an Inpatient-Treatment Program of Major Depression: A Pragmatic Parallel-Group, Randomized Controlled Trial. Psychotherapy and Psychosomatics, 89(4), 258-260. https://doi.org/10.1159/000505855
Generic For Creating Summary Tables
Description
This is an internal function used to create summary table for the different clinical significance methods. This should not be used directly.
Usage
create_summary_table(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments passed to other methods |
Value
A tibble
Create Summary Table for Anchor-Based Approach
Description
Create Summary Table for Anchor-Based Approach
Usage
## S3 method for class 'cs_anchor_individual_within'
create_summary_table(x, data, ...)
Create Summary Table for Combined Approach
Description
Create Summary Table for Combined Approach
Usage
## S3 method for class 'cs_combined'
create_summary_table(
x,
cutoff_results,
data,
method,
r_dd,
se_measurement,
cutoff,
sd_post,
direction,
...
)
Arguments
cutoff_results |
Cutoff results object |
r_dd |
r_dd |
se_measurement |
se_measurement |
cutoff |
Cutoff value |
sd_post |
SD post intervention |
direction |
Which direction is beneficial? 1 = higher, -1 = lower |
Create Summary Table for Distribution-Based Approach
Description
Create Summary Table for Distribution-Based Approach
Usage
## S3 method for class 'cs_distribution'
create_summary_table(x, data, ...)
Arguments
x |
A results object that differs per approach:
|
data |
The used data frame |
... |
Additional arguments |
Create Summary Table for Percentage-Change Approach
Description
Create Summary Table for Percentage-Change Approach
Usage
## S3 method for class 'cs_percentage'
create_summary_table(x, data, ...)
Create Summary Table for Statistical Approach
Description
Create Summary Table for Statistical Approach
Usage
## S3 method for class 'cs_statistical'
create_summary_table(x, data, method, ...)
Arguments
method |
Clinical significance method |
Anchor-Based Analysis of Clinical Significance
Description
cs_anchor()
can be used to determine the clinical significance
of intervention studies employing the anchor-based approach. For this, a
predefined minimally important difference (MID) for an instrument is known
that corresponds to an important symptom improvement for patients. The data
can then be analyzed on the individual as well as the group level to
estimate, if the change because of an intervention is clinically
significant.
Usage
cs_anchor(
data,
id,
time,
outcome,
group,
pre = NULL,
post = NULL,
mid_improvement = NULL,
mid_deterioration = NULL,
better_is = c("lower", "higher"),
target = c("individual", "group"),
effect = c("within", "between"),
bayesian = TRUE,
prior_scale = "medium",
reference_group = NULL,
ci_level = 0.95
)
Arguments
data |
A tidy data frame |
id |
Participant ID |
time |
Time variable |
outcome |
Outcome variable |
group |
Grouping variable (optional) |
pre |
Pre measurement (only needed if the time variable contains more than two measurements) |
post |
Post measurement (only needed if the time variable contains more than two measurements) |
mid_improvement |
Numeric, change that indicates a clinically significant improvement |
mid_deterioration |
Numeric, change that indicates a clinically
significant deterioration (optional). If |
better_is |
Which direction means a better outcome for the used instrument? Available are
|
target |
String, whether an individual or group analysis should be calculated. Available are
|
effect |
String, if
|
bayesian |
Logical, only relevant if |
prior_scale |
String or numeric, can be adjusted to change the Bayesian
prior distribution. See the documentation for |
reference_group |
Specify the reference group to which all subsequent
groups are compared against if |
ci_level |
Numeric, define the credible or confidence interval level. The default is 0.95 for a 95%-CI. |
Value
An S3 object of class cs_analysis
and cs_anchor
Computational details
For the individual-level analyses, the analysis is straight forward. An MID can be specified for an improvement as well as a deterioration (because these must not necessarily be identical) and the function basically counts how many patients fall within the MID range for both, improvement and deterioration, or how many patients exceed the limits of this range in either direction. A patient may than be categorized as:
Improved, the patient demonstrated a change that is equal or greater then the MID for an improvement
Unchanged, the patient demonstrated a change that is less than both MIDs
Deteriorated, the patient demonstrated a change that is equal or greater then the MID for a deterioration
For group-level analyses, the whole sample is either treated as a single group or is split up by grouping presented in the data. For within group analyses, the function calculates the median change from pre to post intervention with the associated credible interval (CI). Based on the median change and the limits of this CI, a group change can be categorized in 5 distinctive categories:
Statistically not significant, the CI contains 0
Statistically significant but not clinically relevant, the CI does not contain 0, but the median and both CI limits are beneath the MID threshold
Not significantly less than the threshold, the MID threshold falls within the CI but the median is still below that threshold
Probably clinically significant effect, the median crossed the MID threshold but the threshold is still inside the CI
Large clinically significant effect, the median crossed the MID threshold and the CI does not contain the threshold
If a between group comparison is desired, a reference group can be defined
with the reference_group
argument to which all subsequent groups are
compared. This is usually an inactive comparator such as a placebo or
wait-list control group. The difference between the pairwise compared
groups is categorized just as the within group difference above, so the
same categories apply.
The approach can be changed to a classical frequentist framework for which the point estimate then represents the mean difference and the CI a confidence interval. For an extensive overview over the differences between a Bayesian and frequentist CI, refer to Hespanhol et al. (2019).
Data preparation
The data set must be tidy, which corresponds to a long data frame in general. It must contain a patient identifier which must be unique per patient. Also, a column containing the different measurements and the outcome must be supplied. Each participant-measurement combination must be unique, so for instance, the data must not contain two "After" measurements for the same patient.
Additionally, if the measurement column contains only two values, the first
value based on alphabetical, numerical or factor ordering will be used as
the pre
measurement. For instance, if the column contains the
measurements identifiers "pre"
and "post"
as strings, then "post"
will be sorted before "pre"
and thus be used as the "pre"
measurement.
The function will throw a warning but generally you may want to explicitly
define the "pre"
and "post"
measurement with arguments pre
and
post
. In case of more than two measurement identifiers, you have to
define pre
and post
manually since the function does not know what your
pre and post intervention measurements are.
If your data is grouped, you can specify the group by referencing the grouping variable (see examples below). The analysis is then run for every group to compare group differences.
References
Hespanhol, L., Vallio, C. S., Costa, L. M., & Saragiotto, B. T. (2019). Understanding and interpreting confidence and credible intervals around effect estimates. Brazilian Journal of Physical Therapy, 23(4), 290–301. https://doi.org/10.1016/j.bjpt.2018.12.006
See Also
Main clinical signficance functions
cs_combined()
,
cs_distribution()
,
cs_percentage()
,
cs_statistical()
Examples
cs_results <- antidepressants |>
cs_anchor(patient, measurement, mom_di, mid_improvement = 8)
cs_results
plot(cs_results)
# Set argument "pre" to avoid a warning
cs_results <- antidepressants |>
cs_anchor(
patient,
measurement,
mom_di,
pre = "Before",
mid_improvement = 8
)
# Inlcude the MID for deterioration
cs_results_with_deterioration <- antidepressants |>
cs_anchor(
patient,
measurement,
mom_di,
pre = "Before",
mid_improvement = 8,
mid_deterioration = 5
)
cs_results_with_deterioration
summary(cs_results_with_deterioration)
plot(cs_results_with_deterioration)
# Group the results by experimental condition
cs_results_grouped <- antidepressants |>
cs_anchor(
patient,
measurement,
mom_di,
pre = "Before",
group = condition,
mid_improvement = 8,
mid_deterioration = 5
)
cs_results_grouped
summary(cs_results_grouped)
plot(cs_results_grouped)
# The plot method always returns a ggplot2 object, so the plot may be further
# modified with ggplot2 code, e.g., facetting to avoid overplotting of groups
plot(cs_results_grouped) +
ggplot2::facet_wrap(~ group)
# Compute group wise results
cs_results_groupwise <- antidepressants |>
cs_anchor(
patient,
measurement,
mom_di,
pre = "Before",
mid_improvement = 8,
target = "group"
)
cs_results_groupwise
summary(cs_results_groupwise)
plot(cs_results_groupwise)
# Group wise analysis, but split by experimentawl condition
cs_results_groupwise_condition <- antidepressants |>
cs_anchor(
patient,
measurement,
mom_di,
pre = "Before",
group = condition,
mid_improvement = 8,
target = "group"
)
cs_results_groupwise_condition
summary(cs_results_groupwise_condition)
plot(cs_results_groupwise_condition)
# Compare all groups to a predefined reference group at a predefined measurement
cs_results_groupwise_between <- antidepressants |>
cs_anchor(
patient,
measurement,
mom_di,
post = "After",
group = condition,
mid_improvement = 8,
target = "group",
effect = "between"
)
cs_results_groupwise_between
summary(cs_results_groupwise_between)
plot(cs_results_groupwise_between)
# Compare all groups to a predefined reference group with frequentist appraoch
cs_results_groupwise_between_freq <- antidepressants |>
cs_anchor(
patient,
measurement,
mom_di,
post = "After",
group = condition,
mid_improvement = 8,
target = "group",
effect = "between",
bayesian = FALSE
)
cs_results_groupwise_between_freq
summary(cs_results_groupwise_between_freq)
plot(cs_results_groupwise_between_freq)
Combined Analysis of Clinical Significance
Description
cs_combined()
can be used to determine the clinical
significance of intervention studies employing the combination of the
distribution-based and statistical approach. For this, it will be assumed
that the functional (non-clinical population) and patient (clinical
population) scores form two distinct distributions on a continuum.
cs_combined()
calculates a cutoff point between these two populations as
well as a reliable change index (RCI) based on a provided instrument
reliability estimate and counts, how many of those patients that showed a
reliable change (that is likely to be not due to measurement error)
switched from the clinical to the functional population during
intervention. Several methods for calculating the cutoff and RCI are
available.
Usage
cs_combined(
data,
id,
time,
outcome,
group = NULL,
pre = NULL,
post = NULL,
mid_improvement = NULL,
mid_deterioration = NULL,
reliability = NULL,
reliability_post = NULL,
m_functional = NULL,
sd_functional = NULL,
better_is = c("lower", "higher"),
rci_method = c("JT", "GLN", "HLL", "EN", "NK", "HA", "HLM"),
cutoff_type = c("a", "b", "c"),
significance_level = 0.05
)
Arguments
data |
A tidy data frame |
id |
Participant ID |
time |
Time variable |
outcome |
Outcome variable |
group |
Grouping variable (optional) |
pre |
Pre measurement (only needed if the time variable contains more than two measurements) |
post |
Post measurement (only needed if the time variable contains more than two measurements) |
mid_improvement |
Numeric, change that indicates a clinically significant improvement |
mid_deterioration |
Numeric, change that indicates a clinically
significant deterioration (optional). If |
reliability |
The instrument's reliability estimate. If you selected the NK method, the here specified reliability will be the instrument's pre measurement reliability. Not needed for the HLM method. |
reliability_post |
The instrument's reliability at post measurement (only needed for the NK method) |
m_functional |
Numeric, mean of functional population. |
sd_functional |
Numeric, standard deviation of functional population |
better_is |
Which direction means a better outcome for the used instrument? Available are
|
rci_method |
Clinical significance method. Available are
|
cutoff_type |
Cutoff type. Available are |
significance_level |
Significance level alpha, defaults to |
Value
An S3 object of class cs_analysis
and cs_combined
Categories
Each individual's change can then be categorized into the following groups:
Recovered, i.e., the individual showed a reliable change in the beneficial direction and changed from the clinical to the functional population
Improved, i.e., the individual showed a reliable change in the beneficial direction but did not change populations
Unchanged, i.e., the individual showed no reliable change
Deteriorated, i.e., the individual showed a reliable change in the disadvantageous direction but did not change populations
Harmed, i.e., the individual showed a reliable change in the disadvantageous direction and switched from the functional to the clinincal population
Computational details
There are three available cutoff types, namely
a, b, and c which can be used to "draw a line" or separate the functional
and clinical population on a continuum. a as a cutoff is defined as the mean
of the clinical population minus two times the standard deviation (SD) of
the clinical population. b is defined as the mean of the functional
population plus also two times the SD of the clinical population. This is
true for "negative" outcomes, where a lower instrument score is desirable.
For "positive" outcomes, where higher scores are beneficial, a is the mean
of the clinical population plus 2 \cdot
SD of the clinical population
and b is mean of the functional population minus 2 \cdot
SD of the
clinical population. The summary statistics for the clinical population are
estimated from the provided data at pre measurement.
c is defined as the midpoint between both populations based on their respective mean and SD. In order to calculate b and c, descriptive statistics for the functional population must be provided.
From the provided data, a region of change is calculated in which an individual change may likely be due to an inherent measurement of the used instrument. This concept is also known as the minimally detectable change (MDC).
Data preparation
The data set must be tidy, which corresponds to a long data frame in general. It must contain a patient identifier which must be unique per patient. Also, a column containing the different measurements and the outcome must be supplied. Each participant-measurement combination must be unique, so for instance, the data must not contain two "After" measurements for the same patient.
Additionally, if the measurement column contains only two values, the first
value based on alphabetical, numerical or factor ordering will be used as
the pre
measurement. For instance, if the column contains the
measurements identifiers "pre"
and "post"
as strings, then "post"
will be sorted before "pre"
and thus be used as the "pre"
measurement.
The function will throw a warning but generally you may want to explicitly
define the "pre"
and "post"
measurement with arguments pre
and
post
. In case of more than two measurement identifiers, you have to
define pre
and post
manually since the function does not know what your
pre and post intervention measurements are.
If your data is grouped, you can specify the group by referencing the grouping variable (see examples below). The analysis is then run for every group to compare group differences.
See Also
Main clinical signficance functions
cs_anchor()
,
cs_distribution()
,
cs_percentage()
,
cs_statistical()
Examples
cs_results <- claus_2020 |>
cs_combined(
id,
time,
bdi,
pre = 1,
post = 4,
reliability = 0.80
)
cs_results
summary(cs_results)
plot(cs_results)
# You can choose a different cutoff but must provide summary statistics for the
# functional population
cs_results_c <- claus_2020 |>
cs_combined(
id,
time,
bdi,
pre = 1,
post = 4,
reliability = 0.80,
m_functional = 8,
sd_functional = 8,
cutoff_type = "c"
)
cs_results_c
summary(cs_results_c)
plot(cs_results_c)
# You can group the analysis by providing a grouping variable in the data
cs_results_grouped <- claus_2020 |>
cs_combined(
id,
time,
bdi,
pre = 1,
post = 4,
group = treatment,
reliability = 0.80,
m_functional = 8,
sd_functional = 8,
cutoff_type = "c"
)
cs_results_grouped
summary(cs_results_grouped)
plot(cs_results_grouped)
Distribution-Based Analysis of Clinical Significance
Description
cs_distribution()
can be used to determine the clinical
significance of intervention studies employing the distribution-based
approach. For this, the reliable change index is estimated from the
provided data and a known reliability estimate which indicates, if an
observed individual change is likely to be greater than the measurement
error inherent for the used instrument. In this case, a reliable change is
defined as clinically significant. Several methods for calculating this RCI
can be chosen.
Usage
cs_distribution(
data,
id,
time,
outcome,
group = NULL,
pre = NULL,
post = NULL,
reliability = NULL,
reliability_post = NULL,
better_is = c("lower", "higher"),
rci_method = c("JT", "GLN", "HLL", "EN", "NK", "HA", "HLM"),
significance_level = 0.05
)
Arguments
data |
A tidy data frame |
id |
Participant ID |
time |
Time variable |
outcome |
Outcome variable |
group |
Grouping variable (optional) |
pre |
Pre measurement (only needed if the time variable contains more than two measurements) |
post |
Post measurement (only needed if the time variable contains more than two measurements) |
reliability |
The instrument's reliability estimate. If you selected the NK method, the here specified reliability will be the instrument's pre measurement reliability. Not needed for the HLM method. |
reliability_post |
The instrument's reliability at post measurement (only needed for the NK method) |
better_is |
Which direction means a better outcome for the used instrument? Available are
|
rci_method |
Clinical significance method. Available are
|
significance_level |
Significance level alpha, defaults to |
Value
An S3 object of class cs_analysis
and cs_distribution
Computational details
From the provided data, a region of change is calculated in which an individual change may likely be due to an inherent measurement of the used instrument. This concept is also known as the minimally detectable change (MDC).
Categories
Each individual's change may then be categorized into one of the following three categories:
Improved, the change is greater than the RCI in the beneficial direction
Unchanged, the change is within a region that may attributable to measurement error
Deteriorated, the change is greater than the RCI, but in the disadvantageous direction
Most of these methods are developed to deal with data containing two
measurements per individual, i.e., a pre intervention and post intervention
measurement. The Hierarchical Linear Modeling (rci_method = "HLM"
) method
can incorporate data for multiple measurements an can thus be used only
for at least three measurements per participant.
Data preparation
The data set must be tidy, which corresponds to a long data frame in general. It must contain a patient identifier which must be unique per patient. Also, a column containing the different measurements and the outcome must be supplied. Each participant-measurement combination must be unique, so for instance, the data must not contain two "After" measurements for the same patient.
Additionally, if the measurement column contains only two values, the first
value based on alphabetical, numerical or factor ordering will be used as
the pre
measurement. For instance, if the column contains the
measurements identifiers "pre"
and "post"
as strings, then "post"
will be sorted before "pre"
and thus be used as the "pre"
measurement.
The function will throw a warning but generally you may want to explicitly
define the "pre"
and "post"
measurement with arguments pre
and
post
. In case of more than two measurement identifiers, you have to
define pre
and post
manually since the function does not know what your
pre and post intervention measurements are.
If your data is grouped, you can specify the group by referencing the grouping variable (see examples below). The analysis is then run for every group to compare group differences.
References
Jacobson, N. S., & Truax, P. (1991). Clinical significance: A statistical approach to defining meaningful change in psychotherapy research. Journal of Consulting and Clinical Psychology, 59(1), 12–19. https://doi.org/10.1037//0022-006X.59.1.12
Hsu, L. M. (1989). Reliable changes in psychotherapy: Taking into account regression toward the mean. Behavioral Assessment, 11(4), 459–467.
Hsu, L. M. (1995). Regression toward the mean associated with measurement error and the identification of improvement and deterioration in psychotherapy. Journal of Consulting and Clinical Psychology, 63(1), 141–144. https://doi.org/10.1037//0022-006x.63.1.141
Speer, D. C. (1992). Clinically significant change: Jacobson and Truax (1991) revisited. Journal of Consulting and Clinical Psychology, 60(3), 402–408. https://doi.org/10.1037/0022-006X.60.3.402
Nunnally, J. C., & Kotsch, W. E. (1983). Studies of individual subjects: Logic and methods of analysis. British Journal of Clinical Psychology, 22(2), 83–93. https://doi.org/10.1111/j.2044-8260.1983.tb00582.x
Hageman, W. J., & Arrindell, W. A. (1999). Establishing clinically significant change: increment of precision and the distinction between individual and group level analysis. Behaviour Research and Therapy, 37(12), 1169–1193. https://doi.org/10.1016/S0005-7967(99)00032-7
Raudenbush, S. W., & Bryk, A. S. (2002). Hierarchical Linear Models - Applications and Data Analysis Methods (2nd ed.). Sage Publications.
See Also
Main clinical signficance functions
cs_anchor()
,
cs_combined()
,
cs_percentage()
,
cs_statistical()
Examples
antidepressants |>
cs_distribution(patient, measurement, mom_di, reliability = 0.80)
# Turn off the warning by providing the pre measurement time
cs_results <- antidepressants |>
cs_distribution(
patient,
measurement,
mom_di,
pre = "Before",
reliability = 0.80
)
summary(cs_results)
plot(cs_results)
# If you use data with more than two measurements, you always have to define a
# pre and post measurement
cs_results <- claus_2020 |>
cs_distribution(
id,
time,
hamd,
pre = 1,
post = 4,
reliability = 0.80
)
cs_results
summary(cs_results)
plot(cs_results)
# Set the rci_method argument to change the RCI method
cs_results_ha <- claus_2020 |>
cs_distribution(
id,
time,
hamd,
pre = 1,
post = 4,
reliability = 0.80,
rci_method = "HA"
)
cs_results_ha
summary(cs_results_ha)
plot(cs_results_ha)
# Group the analysis by providing a grouping variable
cs_results_grouped <- claus_2020 |>
cs_distribution(
id,
time,
hamd,
pre = 1,
post = 4,
group = treatment,
reliability = 0.80
)
cs_results_grouped
summary(cs_results_grouped)
plot(cs_results_grouped)
# Use more than two measurements
cs_results_hlm <- claus_2020 |>
cs_distribution(
id,
time,
hamd,
rci_method = "HLM"
)
cs_results_hlm
summary(cs_results_hlm)
plot(cs_results_hlm)
Extract Augmented Data from a cs_analysis Object
Description
This function returns the patient-wise results, containing the considered pre and post intervention value, its raw change as well as all other change estimates calculated during the clinical significance analysis with the individual's clinical significance category. This function is only useful for individual level analyses because the group level analyses only yield group level results.
Usage
cs_get_augmented_data(x, ...)
## Default S3 method:
cs_get_augmented_data(x, ...)
## S3 method for class 'cs_distribution'
cs_get_augmented_data(x, ...)
## S3 method for class 'cs_statistical'
cs_get_augmented_data(x, ...)
## S3 method for class 'cs_combined'
cs_get_augmented_data(x, ...)
## S3 method for class 'cs_percentage'
cs_get_augmented_data(x, ...)
## S3 method for class 'cs_anchor_individual_within'
cs_get_augmented_data(x, ...)
Arguments
x |
A |
... |
Additional arguments |
Value
A tibble with augmented data
See Also
Extractor functions
cs_get_data()
,
cs_get_model()
,
cs_get_n()
,
cs_get_reliability()
,
cs_get_summary()
Examples
# Augmented data can be extracted for every individual approach
anchor_results <- claus_2020 |>
cs_anchor(
id,
time,
bdi,
pre = 1,
post = 4,
mid_improvement = 9
)
distribution_results <- claus_2020 |>
cs_distribution(
id,
time,
bdi,
pre = 1,
post = 4,
reliability = 0.80
)
distribution_results_hlm <- claus_2020 |>
cs_distribution(
id,
time,
bdi,
rci_method = "HLM"
)
statistical_results <- claus_2020 |>
cs_statistical(
id,
time,
bdi,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 8
)
combined_results <- claus_2020 |>
cs_combined(
id,
time,
bdi,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 8,
reliability = 0.80
)
cs_get_augmented_data(anchor_results)
cs_get_augmented_data(distribution_results)
cs_get_augmented_data(distribution_results_hlm)
cs_get_augmented_data(statistical_results)
cs_get_augmented_data(combined_results)
Get Used Cutoff And Type From A cs_analysis Object
Description
Get Used Cutoff And Type From A cs_analysis Object
Usage
cs_get_cutoff(x, with_descriptives = FALSE)
Arguments
x |
A cs_analysis object |
with_descriptives |
Logical indicating whether you want to retrieve only
the cutoff type and value or the summary statistics on which it is based
on. The default is |
Value
A tibble with cutoff information
Examples
cs_results <- claus_2020 |>
cs_statistical(
id,
time,
bdi,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 8,
cutoff_type = "c"
)
cs_get_cutoff(cs_results)
cs_get_cutoff(cs_results, with_descriptives = TRUE)
Get Descriptives Used In The Cutoff Calculation
Description
Get Descriptives Used In The Cutoff Calculation
Usage
cs_get_cutoff_descriptives(x)
Arguments
x |
A clinisig object |
Value
A tibble with means and standard deviations of the clinical and functional population
Get Data From A cs_analysis Object
Description
Get Data From A cs_analysis Object
Usage
cs_get_data(x, dataset = "data")
Arguments
x |
A cs_analysis object. |
dataset |
The dataset you wish to retrieve. Available options are
|
Value
A tibble
See Also
Extractor functions
cs_get_augmented_data()
,
cs_get_model()
,
cs_get_n()
,
cs_get_reliability()
,
cs_get_summary()
Examples
cs_results <- claus_2020 |>
cs_anchor(id, time, bdi, mid_improvement = 9, pre = 1, post = 4)
cs_get_data(cs_results)
cs_get_data(cs_results, dataset = "wide")
cs_get_data(cs_results, dataset = "original")
Get The HLM Model From A cs_analysis Object
Description
With cs_get_model()
you can extract the fitted HLM model for
the distribution-based approach. This is useful to either diagnose the
model further (beacuse all assumptions of HLMs apply in this case) or plot
the results differently.
Usage
cs_get_model(x)
Arguments
x |
A cs_analysis object |
Value
A model of class lmerMod
See Also
Extractor functions
cs_get_augmented_data()
,
cs_get_data()
,
cs_get_n()
,
cs_get_reliability()
,
cs_get_summary()
Examples
cs_results <- claus_2020 |>
cs_distribution(id, time, bdi, rci_method = "HLM")
cs_get_model(cs_results)
Get Number Of Participants From A cs_analysis Object
Description
With cs_get_n()
one can extract the number of participants
used in a clinical significance analysis from a cs_analysis
object. This
may depend on the clinical significance approach and if missing values were
present in the dataset. For all individual analyses, missing values are
handled by list-wise deletion. Consequently, individuals with a missing pre
or post intervention score will be omitted from the analyses.
Usage
cs_get_n(x, which = "all")
Arguments
x |
A cs_analysis object |
which |
Which n should be returned? Available options are
|
Value
A tibble with number of participants
See Also
Extractor functions
cs_get_augmented_data()
,
cs_get_data()
,
cs_get_model()
,
cs_get_reliability()
,
cs_get_summary()
Examples
# n can be extracted for every approach
cs_results_anchor <- claus_2020 |>
cs_anchor(
id,
time,
bdi,
pre = 1,
post = 4,
mid_improvement = 9
)
cs_results_distribution <- claus_2020 |>
cs_distribution(
id,
time,
bdi,
pre = 1,
post = 4,
reliability = 0.80
)
cs_results_statistical <- claus_2020 |>
cs_statistical(
id,
time,
bdi,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 8,
cutoff_type = "c"
)
cs_results_combined <- claus_2020 |>
cs_combined(
id,
time,
bdi,
pre = 1,
post = 4,
reliability = 0.80,
m_functional = 8,
sd_functional = 8,
cutoff_type = "c"
)
cs_results_percentage <- claus_2020 |>
cs_percentage(
id,
time,
bdi,
pre = 1,
post = 4,
pct_improvement = 0.3
)
cs_get_n(cs_results_anchor)
cs_get_n(cs_results_distribution)
cs_get_n(cs_results_statistical)
cs_get_n(cs_results_combined)
cs_get_n(cs_results_percentage)
# Get your desired n
cs_get_n(cs_results_anchor, which = "all")
cs_get_n(cs_results_anchor, which = "original")
cs_get_n(cs_results_anchor, which = "used")
Get Reliability Of A cs_analysis Object
Description
Get Reliability Of A cs_analysis Object
Usage
cs_get_reliability(x)
Arguments
x |
A cs_analysis object |
Value
A tibble showing the reliability
See Also
Extractor functions
cs_get_augmented_data()
,
cs_get_data()
,
cs_get_model()
,
cs_get_n()
,
cs_get_summary()
Examples
cs_results <- claus_2020 |>
cs_distribution(
id,
time,
bdi,
pre = 1,
post = 4,
reliability = 0.80
)
cs_get_reliability(cs_results)
Get A Summary Table From A cs_analysis Object
Description
Retrieve the summary table in a tidy tibble format. This is especially useful to plot the results or conduct sensitivity analyses.
Usage
cs_get_summary(x, ...)
## Default S3 method:
cs_get_summary(x, which = c("individual", "group"), ...)
## S3 method for class 'cs_anchor_group_within'
cs_get_summary(x, ...)
## S3 method for class 'cs_anchor_group_between'
cs_get_summary(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments passed to the respective method |
which |
Which level of summary table to return. This is only necessary
for method
|
Value
A tibble with clinical significance categories
References
Hageman, W. J., & Arrindell, W. A. (1999). Establishing clinically significant change: increment of precision and the distinction between individual and group level analysis. Behaviour Research and Therapy, 37(12), 1169–1193. https://doi.org/10.1016/S0005-7967(99)00032-7
See Also
Extractor functions
cs_get_augmented_data()
,
cs_get_data()
,
cs_get_model()
,
cs_get_n()
,
cs_get_reliability()
Examples
anchor_results <- claus_2020 |>
cs_anchor(
id,
time,
bdi,
pre = 1,
post = 4,
mid_improvement = 8
)
cs_get_summary(anchor_results)
# Get summary table for a group level analysis
anchor_results_grouped <- claus_2020 |>
cs_anchor(
id,
time,
bdi,
pre = 1,
post = 4,
mid_improvement = 8,
target = "group"
)
cs_get_summary(anchor_results_grouped)
# Get group-wise summary table for the Hageman & Arrindell method
combined_results <- claus_2020 |>
cs_combined(
id,
time,
bdi,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 8,
reliability = 0.80,
rci_method = "HA"
)
cs_get_summary(combined_results)
cs_get_summary(combined_results, which = "group")
Percentage-Change Analysis of Clinical Significance
Description
cs_percentage()
can be used to determine the clinical
significance of intervention studies employing the percentage-change
approach. For this, each individuals relative change compared to the pre
intervention measurement and if this change exceeds a predefined change in
percent points, this change is then deemed clinically significant.
Usage
cs_percentage(
data,
id,
time,
outcome,
group = NULL,
pre = NULL,
post = NULL,
pct_improvement = NULL,
pct_deterioration = NULL,
better_is = c("lower", "higher")
)
Arguments
data |
A tidy data frame |
id |
Participant ID |
time |
Time variable |
outcome |
Outcome variable |
group |
Grouping variable (optional) |
pre |
Pre measurement (only needed if the time variable contains more than two measurements) |
post |
Post measurement (only needed if the time variable contains more than two measurements) |
pct_improvement |
Numeric, percent change that indicates a clinically significant improvement |
pct_deterioration |
Numeric, percent change that indicates a clinically
significant deterioration (optional). If this is not set,
|
better_is |
Which direction means a better outcome for the used instrument? Available are
|
Value
An S3 object of class cs_analysis
and cs_percentage
Computational details
Each participants change is calculated and
then divided by the pre intervention score to estimate the individual's
percent change. A percent change for an improvement as well as a
deterioration can be provided separately and if pct_deterioration
is not
set, it will be assumed to be the same as pct_improvement
.
Categories
Each individual's change may then be categorized into one of the following three categories:
Improved, the change is greater than the predefined percent change in the beneficial direction
Unchanged, the change is within the predefined percent change
Deteriorated, the change is greater than the predefined percent change, but in the disadvantageous direction
Data preparation
The data set must be tidy, which corresponds to a long data frame in general. It must contain a patient identifier which must be unique per patient. Also, a column containing the different measurements and the outcome must be supplied. Each participant-measurement combination must be unique, so for instance, the data must not contain two "After" measurements for the same patient.
Additionally, if the measurement column contains only two values, the first
value based on alphabetical, numerical or factor ordering will be used as
the pre
measurement. For instance, if the column contains the
measurements identifiers "pre"
and "post"
as strings, then "post"
will be sorted before "pre"
and thus be used as the "pre"
measurement.
The function will throw a warning but generally you may want to explicitly
define the "pre"
and "post"
measurement with arguments pre
and
post
. In case of more than two measurement identifiers, you have to
define pre
and post
manually since the function does not know what your
pre and post intervention measurements are.
If your data is grouped, you can specify the group by referencing the grouping variable (see examples below). The analysis is then run for every group to compare group differences.
See Also
Main clinical signficance functions
cs_anchor()
,
cs_combined()
,
cs_distribution()
,
cs_statistical()
Examples
cs_results <- claus_2020 |>
cs_percentage(
id,
time,
hamd,
pre = 1,
post = 4,
pct_improvement = 0.3
)
cs_results
summary(cs_results)
plot(cs_results)
# You can set different thresholds for improvement and deterioration
cs_results_2 <- claus_2020 |>
cs_percentage(
id,
time,
hamd,
pre = 1,
post = 4,
pct_improvement = 0.3,
pct_deterioration = 0.2
)
cs_results_2
summary(cs_results_2)
plot(cs_results_2)
# You can group the analysis by providing a group column from the data
cs_results_grouped <- claus_2020 |>
cs_percentage(
id,
time,
hamd,
pre = 1,
post = 4,
pct_improvement = 0.3,
group = treatment
)
cs_results_grouped
summary(cs_results_grouped)
plot(cs_results_grouped)
# The analyses can be performed for positive outcomes as well, i.e., outcomes
# for which a higher value is beneficial
cs_results_who <- claus_2020 |>
cs_percentage(
id,
time,
who,
pre = 1,
post = 4,
pct_improvement = 0.3,
better_is = "higher"
)
cs_results_who
summary(cs_results_who)
plot(cs_results_who)
plot(cs_results_who, show = category)
Statistical Analysis of Clinical Significance
Description
cs_statistical()
can be used to determine the clinical
significance of intervention studies employing the statistical approach. For
this, it will be assumed that the functional (non-clinical population) and
patient (clinical population) scores form two distinct distributions on a
continuum. cs_statistical()
calculates a cutoff point between these two
populations and counts, how many patients changed from the clinical to the
functional population during intervention. Several methods for calculating
this cutoff are available.
Usage
cs_statistical(
data,
id,
time,
outcome,
group = NULL,
pre = NULL,
post = NULL,
m_functional = NULL,
sd_functional = NULL,
reliability = NULL,
better_is = c("lower", "higher"),
cutoff_method = c("JT", "HA"),
cutoff_type = c("a", "b", "c"),
significance_level = 0.05
)
Arguments
data |
A tidy data frame |
id |
Participant ID |
time |
Time variable |
outcome |
Outcome variable |
group |
Grouping variable (optional) |
pre |
Pre measurement (only needed if the time variable contains more than two measurements) |
post |
Post measurement (only needed if the time variable contains more than two measurements) |
m_functional |
Numeric, mean of functional population. |
sd_functional |
Numeric, standard deviation of functional population |
reliability |
The instrument's reliability estimate. If you selected the NK method, the here specified reliability will be the instrument's pre measurement reliability. Not needed for the HLM method. |
better_is |
Which direction means a better outcome for the used instrument? Available are
|
cutoff_method |
Cutoff method, Available are
|
cutoff_type |
Cutoff type. Available are |
significance_level |
Significance level alpha, defaults to |
Value
An S3 object of class cs_analysis
and cs_statistical
Computational details
There are three available cutoff types, namely
a, b, and c which can be used to "draw a line" or separate the functional
and clinical population on a continuum. a as a cutoff is defined as the mean
of the clinical population minus two times the standard deviation (SD) of
the clinical population. b is defined as the mean of the functional
population plus also two times the SD of the clinical population. This is
true for "negative" outcomes, where a lower instrument score is desirable.
For "positive" outcomes, where higher scores are beneficial, a is the mean
of the clinical population plus 2 \cdot
SD of the clinical population
and b is mean of the functional population minus 2 \cdot
SD of the
clinical population. The summary statistics for the clinical population are
estimated from the provided data at pre measurement.
c is defined as the midpoint between both populations based on their respective mean and SD. In order to calculate b and c, descriptive statistics for the functional population must be provided.
Categories
Individual patients can be categorized into one of the following groups:
Improved, i.e., one changed from the clinical to the functional population
Unchanged, i.e., one can be seen as a member of the same population pre and post intervention
Deteriorated, i.e., one changed from the functional to the clinical population during intervention
Data preparation
The data set must be tidy, which corresponds to a long data frame in general. It must contain a patient identifier which must be unique per patient. Also, a column containing the different measurements and the outcome must be supplied. Each participant-measurement combination must be unique, so for instance, the data must not contain two "After" measurements for the same patient.
Additionally, if the measurement column contains only two values, the first
value based on alphabetical, numerical or factor ordering will be used as
the pre
measurement. For instance, if the column contains the
measurements identifiers "pre"
and "post"
as strings, then "post"
will be sorted before "pre"
and thus be used as the "pre"
measurement.
The function will throw a warning but generally you may want to explicitly
define the "pre"
and "post"
measurement with arguments pre
and
post
. In case of more than two measurement identifiers, you have to
define pre
and post
manually since the function does not know what your
pre and post intervention measurements are.
If your data is grouped, you can specify the group by referencing the grouping variable (see examples below). The analysis is then run for every group to compare group differences.
References
Jacobson, N. S., & Truax, P. (1991). Clinical significance: A statistical approach to defining meaningful change in psychotherapy research. Journal of Consulting and Clinical Psychology, 59(1), 12–19. https://doi.org/10.1037//0022-006X.59.1.12
Hageman, W. J., & Arrindell, W. A. (1999). Establishing clinically significant change: increment of precision and the distinction between individual and group level analysis. Behaviour Research and Therapy, 37(12), 1169–1193. https://doi.org/10.1016/S0005-7967(99)00032-7
See Also
Main clinical signficance functions
cs_anchor()
,
cs_combined()
,
cs_distribution()
,
cs_percentage()
Examples
# By default, cutoff type "a" is used
cs_results <- claus_2020 |>
cs_statistical(id, time, hamd, pre = 1, post = 4)
cs_results
summary(cs_results)
plot(cs_results)
# You can choose a different cutoff type but need to provide additional
# population summary statistics for the functional population
cs_results_c <- claus_2020 |>
cs_statistical(
id,
time,
hamd,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 8,
cutoff_type = "c"
)
cs_results_c
summary(cs_results_c)
plot(cs_results_c)
# You can use a different method to calculate the cutoff
cs_results_ha <- claus_2020 |>
cs_statistical(
id,
time,
hamd,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 8,
reliability = 0.80,
cutoff_type = "c",
cutoff_method = "HA"
)
cs_results_ha
summary(cs_results_ha)
plot(cs_results_ha)
# And you can group the analysis by providing a grouping variable from the data
cs_results_grouped <- claus_2020 |>
cs_statistical(
id,
time,
hamd,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 8,
cutoff_type = "c",
group = treatment
)
cs_results_grouped
summary(cs_results_grouped)
plot(cs_results_grouped)
Generic to Calculate RCI Band Data for Plotting
Description
This is an internal generic to generate data for the RCI band in clinical significance plots. This should not be called directly.
Usage
generate_plotting_band(x, lower_limit, upper_limit, ...)
Arguments
x |
An object of respective class |
lower_limit |
Lower plotting limit |
upper_limit |
Upper plotting limit |
... |
Additional arguments |
Value
A tibble with data for the ribbon indicating unchanged patients
Generate RCI Band for the Individual Anchor-Based Approach
Description
Generate RCI Band for the Individual Anchor-Based Approach
Usage
## S3 method for class 'cs_anchor_individual_within'
generate_plotting_band(x, lower_limit = 0, upper_limit = 100, ...)
Generate RCI Band for EN Method
Description
Generate RCI Band for EN Method
Usage
## S3 method for class 'cs_en'
generate_plotting_band(x, lower_limit = 0, upper_limit = 100, ...)
Generate RCI Band for GLN Method
Description
Generate RCI Band for GLN Method
Usage
## S3 method for class 'cs_gln'
generate_plotting_band(x, lower_limit = 0, upper_limit = 100, ...)
Generate RCI Band for HA Method
Description
Generate RCI Band for HA Method
Usage
## S3 method for class 'cs_ha'
generate_plotting_band(x, lower_limit = 0, upper_limit = 100, ...)
Generate RCI Band for HLL Method
Description
Generate RCI Band for HLL Method
Usage
## S3 method for class 'cs_hll'
generate_plotting_band(x, lower_limit = 0, upper_limit = 100, ...)
Generate RCI Band for JT Method
Description
Generate RCI Band for JT Method
Usage
## S3 method for class 'cs_jt'
generate_plotting_band(x, lower_limit = 0, upper_limit = 100, ...)
Generate RCI Band for NK Method
Description
Generate RCI Band for NK Method
Usage
## S3 method for class 'cs_nk'
generate_plotting_band(x, lower_limit = 0, upper_limit = 100, ...)
Generate RCI Band for the Percentage-Change Approach
Description
Generate RCI Band for the Percentage-Change Approach
Usage
## S3 method for class 'cs_percentage'
generate_plotting_band(x, lower_limit = 0, upper_limit = 100, ...)
Chronic Pain Data
Description
A reduced version of the data collected by Hechler et al. (2014)
Usage
hechler_2014
Format
A tibble with 208 rows and 3 variables:
patient
Patient identifier
measurement
Indicator of measurement
disability
Pain-related disability as measured with the PPDI (lower is better)
References
Hechler, T., Ruhe, A.‑K., Schmidt, P., Hirsch, J., Wager, J., Dobe, M., Krummenauer, F., & Zernikow, B. (2014). Inpatient Based Intensive Interdisciplinary Pain Treatment for Highly Impaired Children with Severe Chronic Pain: Randomized Controlled Trial of Efficacy and Economic Effects. Pain, 155(1), 118–128. https://doi.org/10.1016/j.pain.2013.09.015
Marital Therapy Data
Description
A dataset containing the data from Jacobson et al. (1989). The purpose of the study was to examine two forms of behavioral marital therapy,
Usage
jacobson_1989
Format
An object of class tbl_df
with 60 rows and 4 columns.
- subject
Subject ID
- time
Measurement
- das
Dyadic Adjustment Scale score (higher is better)
- gds
Global Distress Scale score (lower is better)
References
Jacobson, N. S., Schmaling, K. B., Holtzworth-Munroe, A., Katt, J. L., Wood, L. F., & Follette, V. M. (1989). Research-structured vs clinically flexible versions of social learning-based marital therapy. Behaviour Research and Therapy, 27(2), 173-180. https://doi.org/10.1016/0005-7967(89)90076-4
Jacobson, N. S., & Truax, P. (1991). Clinical significance: A statistical approach to defining meaningful change in psychotherapy research. Journal of Consulting and Clinical Psychology, 59(1), 12-19. https://doi.org/10.1037//0022-006X.59.1.12
Plot an Object of Class cs_anchor_group_between
Description
This function creates a generic group level clinical significance plot by plotting the between group change with the associated uncertainty interval around the estimated change on the y-axis.
Usage
## S3 method for class 'cs_anchor_group_between'
plot(
x,
x_lab = "Group",
y_lab = "Mean Intervention Effect\n(with 95%-CI)",
...
)
Arguments
x |
An object of class |
x_lab |
String, x axis label, defaults to |
y_lab |
String, y axis label, defaults to |
... |
Additional arguments |
Value
A ggplot2 plot
Examples
cs_results <- antidepressants |>
cs_anchor(
patient,
measurement,
mom_di,
mid_improvement = 8,
target = "group",
group = condition,
effect = "between",
post = "After"
)
# Plot the results "as is"
plot(cs_results)
# Change the axis labels
plot(cs_results, x_lab = "Condition", y_lab = "Treatment Effect")
Plot an Object of Class cs_anchor_group_within
Description
This function creates a generic group level clinical significance plot by plotting the within group change with the associated uncertainty interval around the estimated change on the y-axis.
Usage
## S3 method for class 'cs_anchor_group_within'
plot(
x,
x_lab = "Group",
y_lab = "Mean Intervention Effect\n(with 95%-CI)",
...
)
Arguments
x |
An object of class |
x_lab |
String, x axis label. Defaults to |
y_lab |
String, y axis label, defaults to |
... |
Additional arguments |
Value
A ggplot2 plot
Examples
cs_results <- antidepressants |>
cs_anchor(
patient,
measurement,
mom_di,
mid_improvement = 8,
target = "group",
group = condition
)
# Plot the results "as is"
plot(cs_results)
# Change the axis labels
plot(cs_results, x_lab = "Condition", y_lab = "Treatment Effect")
Plot an Object of Class cs_anchor_individual_within
Description
This function creates a generic clinical significance plot by plotting the patients' pre intervention value on the x-axis and the post intervention score on the y-axis.
Usage
## S3 method for class 'cs_anchor_individual_within'
plot(
x,
x_lab = "Pre",
y_lab = "Post",
color_lab = "Group",
lower_limit,
upper_limit,
show,
point_alpha = 1,
mid_fill = "grey10",
mid_alpha = 0.1,
overplotting = 0.02,
...
)
Arguments
x |
An object of class |
x_lab |
String, x axis label. Default is |
y_lab |
String, x axis label. Default is |
color_lab |
String, color label (if colors are displayed). Default is
|
lower_limit |
Numeric, lower plotting limit. Defaults to 2% smaller than minimum instrument score |
upper_limit |
Numeric, upper plotting limit. Defaults to 2% larger than maximum instrument score |
show |
Unquoted category name. You have several options to color different features. Available are
|
point_alpha |
Numeric, transparency adjustment for points. A value between 0 and 1 where 1 corresponds to not transparent at all and 0 to fully transparent. |
mid_fill |
String, a color (name or HEX code) for the percentage range fill |
mid_alpha |
Numeric, controls the transparency of the percentage fill. This can be any value between 0 and 1, defaults to 0.1 |
overplotting |
Numeric, control amount of overplotting. Defaults to 0.02 (i.e., 2% of range between lower and upper limit). |
... |
Additional arguments |
Value
A ggplot2 plot
Examples
cs_results <- antidepressants |>
cs_anchor(
patient,
measurement,
pre = "Before",
mom_di,
mid_improvement = 8
)
# Plot the results "as is"
plot(cs_results)
# Change the axis labels
plot(cs_results, x_lab = "Before Intervention", y_lab = "After Intervention")
# Show the individual categories
plot(cs_results, show = category)
# Show a specific category
plot(cs_results, show = improved)
# Show groups as specified in the data
cs_results_grouped <- antidepressants |>
cs_anchor(
patient,
measurement,
pre = "Before",
mom_di,
mid_improvement = 8,
group = condition
)
plot(cs_results_grouped)
# To avoid overplotting, generic ggplot2 code can be used to facet the plot
library(ggplot2)
plot(cs_results_grouped) +
facet_wrap(~ group)
# Adjust the transparency of individual data points
plot(cs_results, point_alpha = 0.3)
# Adjust the fill and transparency of the "unchanged" (PCC) region
plot(cs_results, mid_fill = "firebrick", mid_alpha = 0.2)
# Control the overplotting
plot(cs_results, overplotting = 0.1)
# Or adjust the axis limits by hand
plot(cs_results, lower_limit = 0, upper_limit = 80)
Plot an Object of Class cs_combined
Description
This function creates a generic clinical significance plot by plotting the patients' pre intervention value on the x-axis and the post intervention score on the y-axis.
Usage
## S3 method for class 'cs_combined'
plot(
x,
x_lab = NULL,
y_lab = NULL,
color_lab = "Group",
lower_limit,
upper_limit,
show,
point_alpha = 1,
trajectory_alpha = 1,
rci_fill = "grey10",
rci_alpha = 0.1,
overplotting = 0.02,
...
)
Arguments
x |
An object of class |
x_lab |
String, x axis label. Default is |
y_lab |
String, x axis label. Default is |
color_lab |
String, color label (if colors are displayed). Default is
|
lower_limit |
Numeric, lower plotting limit. Defaults to 2% smaller than minimum instrument score |
upper_limit |
Numeric, upper plotting limit. Defaults to 2% larger than maximum instrument score |
show |
Unquoted category name. You have several options to color different features. Available are
|
point_alpha |
Numeric, transparency adjustment for points. A value between 0 and 1 where 1 corresponds to not transparent at all and 0 to fully transparent. |
trajectory_alpha |
Numeric, transparency adjustment for trajectories. A value between 0 and 1 where 1 corresponds to not transparent at all and 0 to fully transparent. |
rci_fill |
String, a color (name or HEX code) for RCI fill |
rci_alpha |
Numeric, controls the transparency of the RCI. This can be any value between 0 and 1, defaults to 0.1 |
overplotting |
Numeric, control amount of overplotting. Defaults to 0.02 (i.e., 2% of range between lower and upper limit). |
... |
Additional arguments |
Value
A ggplot2 plot
Examples
cs_results <- antidepressants |>
cs_combined(
patient,
measurement,
pre = "Before",
mom_di,
reliability = 0.80,
m_functional = 15,
sd_functional = 8,
cutoff_type = "c"
)
# Plot the results "as is"
plot(cs_results)
# Change the axis labels
plot(cs_results, x_lab = "Before Intervention", y_lab = "After Intervention")
# Show the individual categories
plot(cs_results, show = category)
# Show a specific
plot(cs_results, show = recovered)
# Show groups as specified in the data
cs_results_grouped <- antidepressants |>
cs_combined(
patient,
measurement,
pre = "Before",
mom_di,
reliability = 0.80,
m_functional = 15,
sd_functional = 8,
cutoff_type = "c",
group = condition
)
plot(cs_results_grouped)
# To avoid overplotting, generic ggplot2 code can be used to facet the plot
library(ggplot2)
plot(cs_results_grouped) +
facet_wrap(~ group)
# Adjust the transparency of individual data points
plot(cs_results, point_alpha = 0.3)
# Adjust the fill and transparency of the "unchanged" (RCI) region
plot(cs_results, rci_fill = "firebrick", rci_alpha = 0.2)
# Control the overplotting
plot(cs_results, overplotting = 0.1)
# Or adjust the axis limits by hand
plot(cs_results, lower_limit = 0, upper_limit = 80)
Plot an Object of Class cs_distribution
Description
This function creates a generic clinical significance plot by plotting the patients' pre intervention value on the x-axis and the post intervention score on the y-axis.
Usage
## S3 method for class 'cs_distribution'
plot(
x,
x_lab = NULL,
y_lab = NULL,
color_lab = "Group",
lower_limit,
upper_limit,
show,
point_alpha = 1,
trajectory_alpha = 1,
rci_fill = "grey10",
rci_alpha = 0.1,
overplotting = 0.02,
...
)
Arguments
x |
An object of class |
x_lab |
String, x axis label. Default is |
y_lab |
String, x axis label. Default is |
color_lab |
String, color label (if colors are displayed). Default is
|
lower_limit |
Numeric, lower plotting limit. Defaults to 2% smaller than minimum instrument score |
upper_limit |
Numeric, upper plotting limit. Defaults to 2% larger than maximum instrument score |
show |
Unquoted category name. You have several options to color different features. Available are
|
point_alpha |
Numeric, transparency adjustment for points. A value between 0 and 1 where 1 corresponds to not transparent at all and 0 to fully transparent. |
trajectory_alpha |
Numeric, transparency adjustment for trajectories. A value between 0 and 1 where 1 corresponds to not transparent at all and 0 to fully transparent. |
rci_fill |
String, a color (name or HEX code) for RCI fill |
rci_alpha |
Numeric, controls the transparency of the RCI. This can be any value between 0 and 1, defaults to 0.1 |
overplotting |
Numeric, control amount of overplotting. Defaults to 0.02 (i.e., 2% of range between lower and upper limit). |
... |
Additional arguments |
Value
A ggplot2 plot
Examples
cs_results <- antidepressants |>
cs_distribution(
patient,
measurement,
pre = "Before",
mom_di,
reliability = 0.80
)
# Plot the results "as is"
plot(cs_results)
# Change the axis labels
plot(cs_results, x_lab = "Before Intervention", y_lab = "After Intervention")
# Show the individual categories
plot(cs_results, show = category)
# Show a specific
plot(cs_results, show = improved)
# Show groups as specified in the data
cs_results_grouped <- antidepressants |>
cs_distribution(
patient,
measurement,
pre = "Before",
mom_di,
reliability = 0.80,
group = condition
)
plot(cs_results_grouped)
# To avoid overplotting, generic ggplot2 code can be used to facet the plot
library(ggplot2)
plot(cs_results_grouped) +
facet_wrap(~ group)
# Adjust the transparency of individual data points
plot(cs_results, point_alpha = 0.3)
# Adjust the fill and transparency of the "unchanged" (RCI) region
plot(cs_results, rci_fill = "firebrick", rci_alpha = 0.2)
# Control the overplotting
plot(cs_results, overplotting = 0.1)
# Or adjust the axis limits by hand
plot(cs_results, lower_limit = 0, upper_limit = 80)
Plot an Object of Class cs_percentage
Description
This function creates a generic clinical significance plot by plotting the patients' pre intervention value on the x-axis and the post intervention score on the y-axis.
Usage
## S3 method for class 'cs_percentage'
plot(
x,
x_lab = "Pre",
y_lab = "Post",
color_lab = "Group",
lower_limit,
upper_limit,
show,
point_alpha = 1,
pct_fill = "grey10",
pct_alpha = 0.1,
overplotting = 0.02,
...
)
Arguments
x |
An object of class |
x_lab |
String, x axis label. Default is |
y_lab |
String, x axis label. Default is |
color_lab |
String, color label (if colors are displayed). Default is
|
lower_limit |
Numeric, lower plotting limit. Defaults to 2% smaller than minimum instrument score |
upper_limit |
Numeric, upper plotting limit. Defaults to 2% larger than maximum instrument score |
show |
Unquoted category name. You have several options to color different features. Available are
|
point_alpha |
Numeric, transparency adjustment for points. A value between 0 and 1 where 1 corresponds to not transparent at all and 0 to fully transparent. |
pct_fill |
String, a color (name or HEX code) for the percentage range fill |
pct_alpha |
Numeric, controls the transparency of the percentage fill. This can be any value between 0 and 1, defaults to 0.1 |
overplotting |
Numeric, control amount of overplotting. Defaults to 0.02 (i.e., 2% of range between lower and upper limit). |
... |
Additional arguments |
Value
A ggplot2 plot
Examples
cs_results <- antidepressants |>
cs_percentage(
patient,
measurement,
pre = "Before",
mom_di,
pct_improvement = 0.4
)
# Plot the results "as is"
plot(cs_results)
# Change the axis labels
plot(cs_results, x_lab = "Before Intervention", y_lab = "After Intervention")
# Show the individual categories
plot(cs_results, show = category)
# Show a specific category
plot(cs_results, show = improved)
# Show groups as specified in the data
cs_results_grouped <- antidepressants |>
cs_percentage(
patient,
measurement,
pre = "Before",
mom_di,
pct_improvement = 0.4,
group = condition
)
plot(cs_results_grouped)
# To avoid overplotting, generic ggplot2 code can be used to facet the plot
library(ggplot2)
plot(cs_results_grouped) +
facet_wrap(~ group)
# Adjust the transparency of individual data points
plot(cs_results, point_alpha = 0.3)
# Adjust the fill and transparency of the "unchanged" (PCC) region
plot(cs_results, pct_fill = "firebrick", pct_alpha = 0.2)
# Control the overplotting
plot(cs_results, overplotting = 0.1)
# Or adjust the axis limits by hand
plot(cs_results, lower_limit = 0, upper_limit = 80)
Plot an Object of Class cs_statistical
Description
This function creates a generic clinical significance plot by plotting the patients' pre intervention value on the x-axis and the post intervention score on the y-axis.
Usage
## S3 method for class 'cs_statistical'
plot(
x,
x_lab = "Pre",
y_lab = "Post",
color_lab = "Group",
include_cutoff = TRUE,
lower_limit,
upper_limit,
show,
point_alpha = 1,
overplotting = 0.02,
...
)
Arguments
x |
An object of class |
x_lab |
String, x axis label. Default is |
y_lab |
String, x axis label. Default is |
color_lab |
String, color label (if colors are displayed). Default is
|
include_cutoff |
Logical, whether to include the population cutoff.
Default is |
lower_limit |
Numeric, lower plotting limit. Defaults to 2% smaller than minimum instrument score |
upper_limit |
Numeric, upper plotting limit. Defaults to 2% larger than maximum instrument score |
show |
Unquoted category name. You have several options to color different features. Available are
|
point_alpha |
Numeric, transparency adjustment for points. A value between 0 and 1 where 1 corresponds to not transparent at all and 0 to fully transparent. |
overplotting |
Numeric, control amount of overplotting. Defaults to 0.02 (i.e., 2% of range between lower and upper limit). |
... |
Additional arguments |
Value
A ggplot2 plot
Examples
cs_results <- antidepressants |>
cs_statistical(
patient,
measurement,
pre = "Before",
mom_di,
m_functional = 15,
sd_functional = 8,
cutoff_type = "c"
)
# Plot the results "as is"
plot(cs_results)
# Change the axis labels
plot(cs_results, x_lab = "Before Intervention", y_lab = "After Intervention")
# Show the individual categories
plot(cs_results, show = category)
# Show groups as specified in the data
cs_results_grouped <- antidepressants |>
cs_statistical(
patient,
measurement,
pre = "Before",
mom_di,
m_functional = 15,
sd_functional = 8,
cutoff_type = "c",
group = condition
)
plot(cs_results_grouped)
# To avoid overplotting, generic ggplot2 code can be used to facet the plot
library(ggplot2)
plot(cs_results_grouped) +
facet_wrap(~ group)
# Adjust the transparency of individual data points
plot(cs_results, point_alpha = 0.3)
# Control the overplotting
plot(cs_results, overplotting = 0.1)
# Or adjust the axis limits by hand
plot(cs_results, lower_limit = 0, upper_limit = 80)
Print Method for the Anchor-Based Approach for Groups (Between)
Description
Print Method for the Anchor-Based Approach for Groups (Between)
Usage
## S3 method for class 'cs_anchor_group_between'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects
Examples
cs_results <- claus_2020 |>
cs_anchor(
id,
time,
bdi,
post = 4,
mid_improvement = 7,
group = treatment,
target = "group",
effect = "between"
)
cs_results
Print Method for the Anchor-Based Approach for Groups (Within)
Description
Print Method for the Anchor-Based Approach for Groups (Within)
Usage
## S3 method for class 'cs_anchor_group_within'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects
Examples
cs_results <- claus_2020 |>
cs_anchor(
id,
time,
bdi,
pre = 1,
post = 4,
mid_improvement = 7,
target = "group"
)
cs_results
Print Method for the Anchor-Based Approach for Individuals
Description
Print Method for the Anchor-Based Approach for Individuals
Usage
## S3 method for class 'cs_anchor_individual_within'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects
Examples
cs_results <- claus_2020 |>
cs_distribution(id, time, hamd, pre = 1, post = 4, reliability = 0.8)
cs_results
Print Method for the Combined Approach
Description
Print Method for the Combined Approach
Usage
## S3 method for class 'cs_combined'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects
Examples
cs_results <- claus_2020 |>
cs_combined(id, time, hamd, pre = 1, post = 4, reliability = 0.8)
cs_results
Print Method for the Distribution-Based Approach
Description
Print Method for the Distribution-Based Approach
Usage
## S3 method for class 'cs_distribution'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects
Examples
cs_results <- claus_2020 |>
cs_distribution(id, time, hamd, pre = 1, post = 4, reliability = 0.8)
cs_results
Print Method for the Percentange-Change Approach
Description
Print Method for the Percentange-Change Approach
Usage
## S3 method for class 'cs_percentage'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects
Examples
cs_results <- claus_2020 |>
cs_percentage(
id,
time,
bdi,
pre = 1,
post = 4,
pct_improvement = 0.5
)
cs_results
Print Method for the Statistical Approach
Description
Print Method for the Statistical Approach
Usage
## S3 method for class 'cs_statistical'
print(x, ...)
Arguments
x |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects
Examples
cs_results <- claus_2020 |>
cs_statistical(
id,
time,
hamd,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 7
)
cs_results
Summary Method for the Anchor-Based Approach for Groups (Between)
Description
Summary Method for the Anchor-Based Approach for Groups (Between)
Usage
## S3 method for class 'cs_anchor_group_between'
summary(object, ...)
Arguments
object |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects only
Examples
cs_results <- antidepressants |>
cs_anchor(
patient,
measurement,
post = "After",
mom_di,
mid_improvement = 8,
target = "group",
effect = "between",
group = condition
)
summary(cs_results)
Summary Method for the Anchor-Based Approach for Groups (Within)
Description
Summary Method for the Anchor-Based Approach for Groups (Within)
Usage
## S3 method for class 'cs_anchor_group_within'
summary(object, ...)
Arguments
object |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects only
Examples
cs_results <- claus_2020 |>
cs_anchor(
id,
time,
bdi,
pre = 1,
post = 4,
mid_improvement = 8,
target = "group"
)
summary(cs_results)
Summary Method for the Anchor-Based Approach
Description
Summary Method for the Anchor-Based Approach
Usage
## S3 method for class 'cs_anchor_individual_within'
summary(object, ...)
Arguments
object |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects only
Examples
cs_results <- claus_2020 |>
cs_anchor(
id,
time,
bdi,
pre = 1,
post = 4,
mid_improvement = 7
)
cs_results
Summary Method for the Combined Approach
Description
Summary Method for the Combined Approach
Usage
## S3 method for class 'cs_combined'
summary(object, ...)
Arguments
object |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects only
Examples
cs_results <- claus_2020 |>
cs_combined(id, time, hamd, pre = 1, post = 4, reliability = 0.8)
summary(cs_results)
Summary Method for the Distribution-Based Approach
Description
Summary Method for the Distribution-Based Approach
Usage
## S3 method for class 'cs_distribution'
summary(object, ...)
Arguments
object |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects only
Examples
cs_results <- claus_2020 |>
cs_distribution(id, time, hamd, pre = 1, post = 4, reliability = 0.8)
summary(cs_results)
Summary Method for the Percentage-Change Approach
Description
Summary Method for the Percentage-Change Approach
Usage
## S3 method for class 'cs_percentage'
summary(object, ...)
Arguments
object |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects only
Examples
cs_results <- claus_2020 |>
cs_percentage(
id,
time,
bdi,
pre = 1,
post = 4,
pct_improvement = 0.5
)
summary(cs_results)
Summary Method for the Statistical Approach
Description
Summary Method for the Statistical Approach
Usage
## S3 method for class 'cs_statistical'
summary(object, ...)
Arguments
object |
An object of class |
... |
Additional arguments |
Value
No return value, called for side effects only
Examples
cs_results <- claus_2020 |>
cs_statistical(
id,
time,
hamd,
pre = 1,
post = 4,
m_functional = 8,
sd_functional = 7
)
summary(cs_results)