The University of Southampton
University of Southampton Institutional Repository

Multilevel analyses of on-demand medication data, with an application to the treatment of Female Sexual Interest/Arousal Disorder

Multilevel analyses of on-demand medication data, with an application to the treatment of Female Sexual Interest/Arousal Disorder
Multilevel analyses of on-demand medication data, with an application to the treatment of Female Sexual Interest/Arousal Disorder
Data from clinical trials investigating on-demand medication often consist of an intentionally varying number of measurements per patient. These measurements are often observations of discrete events of when the medication was taken, including for example data on symptom severity. In addition to the varying number of observations between patients, the data have another important feature: they are characterized by a hierarchical structure in which the events are nested within patients. Traditionally, the observed events of patients are aggregated into means and subsequently analyzed using, for example, a repeated measures ANOVA. This procedure has drawbacks. One drawback is that these patient means have different standard errors, first, because the variance of the underlying events differs between patients and second, because the number of events per patient differs. In this paper, we argue that such data should be analyzed by applying a multilevel analysis using the individual observed events as separate nested observations. Such a multilevel approach handles this drawback and it also enables the examination of varying drug effects across
patients by estimating random effects. We show how multilevel analyses can be applied to on-demand medication data from a clinical trial investigating the efficacy of a drug for women with low sexual desire. We also explore linear and quadratic time effects that can only be performed when the individual events are considered as separate observations and we discuss several important statistical topics relevant for multilevel modeling. Taken together, the use of a multilevel approach considering events as nested observations in these types of data is advocated as it is more valid and provides more information than other
(traditional) methods.
1932-6203
1-22
Kessels, Rob
e01f5370-c566-4ce0-8679-03256c6e8e68
Bloemers, Jos
2034920c-07df-4c53-bb27-6a729dbec3e9
Tuiten, Adriaan
c126e55b-bff8-46a1-a4ed-489032e1e3e0
Van Der Heijden, Peter G. M.
85157917-3b33-4683-81be-713f987fd612
Ferrer, Rodrigo
0757ea29-723f-4fd6-b725-c69e4a032966
Kessels, Rob
e01f5370-c566-4ce0-8679-03256c6e8e68
Bloemers, Jos
2034920c-07df-4c53-bb27-6a729dbec3e9
Tuiten, Adriaan
c126e55b-bff8-46a1-a4ed-489032e1e3e0
Van Der Heijden, Peter G. M.
85157917-3b33-4683-81be-713f987fd612
Ferrer, Rodrigo
0757ea29-723f-4fd6-b725-c69e4a032966

Kessels, Rob, Bloemers, Jos, Tuiten, Adriaan and Van Der Heijden, Peter G. M. , Ferrer, Rodrigo (ed.) (2019) Multilevel analyses of on-demand medication data, with an application to the treatment of Female Sexual Interest/Arousal Disorder. PLoS ONE, 14 (8), 1-22, [e0221063]. (doi:10.1371/journal.pone.0221063).

Record type: Article

Abstract

Data from clinical trials investigating on-demand medication often consist of an intentionally varying number of measurements per patient. These measurements are often observations of discrete events of when the medication was taken, including for example data on symptom severity. In addition to the varying number of observations between patients, the data have another important feature: they are characterized by a hierarchical structure in which the events are nested within patients. Traditionally, the observed events of patients are aggregated into means and subsequently analyzed using, for example, a repeated measures ANOVA. This procedure has drawbacks. One drawback is that these patient means have different standard errors, first, because the variance of the underlying events differs between patients and second, because the number of events per patient differs. In this paper, we argue that such data should be analyzed by applying a multilevel analysis using the individual observed events as separate nested observations. Such a multilevel approach handles this drawback and it also enables the examination of varying drug effects across
patients by estimating random effects. We show how multilevel analyses can be applied to on-demand medication data from a clinical trial investigating the efficacy of a drug for women with low sexual desire. We also explore linear and quadratic time effects that can only be performed when the individual events are considered as separate observations and we discuss several important statistical topics relevant for multilevel modeling. Taken together, the use of a multilevel approach considering events as nested observations in these types of data is advocated as it is more valid and provides more information than other
(traditional) methods.

Text
journal.pone.0221063 - Version of Record
Available under License Creative Commons Attribution.
Download (2MB)
Other
RE Recently accepted outputs
Restricted to Repository staff only
Request a copy

More information

Accepted/In Press date: 29 July 2019
e-pub ahead of print date: 15 August 2019

Identifiers

Local EPrints ID: 433484
URI: http://eprints.soton.ac.uk/id/eprint/433484
ISSN: 1932-6203
PURE UUID: cfd2a537-9619-4486-abee-3c597969cb99
ORCID for Peter G. M. Van Der Heijden: ORCID iD orcid.org/0000-0002-3345-096X

Catalogue record

Date deposited: 23 Aug 2019 16:30
Last modified: 16 Mar 2024 04:14

Export record

Altmetrics

Contributors

Author: Rob Kessels
Author: Jos Bloemers
Author: Adriaan Tuiten
Editor: Rodrigo Ferrer

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×