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Discrete- vs. Continuous-Time Modeling of Unequally Spaced Experience Sampling Method Data

The Experience Sampling Method is a common approach in psychological research for collecting intensive longitudinal data with high ecological validity. One characteristic of ESM data is that it is often unequally spaced, because the measurement intervals within a day are deliberately varied, and mea...

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Autores principales: de Haan-Rietdijk, Silvia, Voelkle, Manuel C., Keijsers, Loes, Hamaker, Ellen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655034/
https://www.ncbi.nlm.nih.gov/pubmed/29104554
http://dx.doi.org/10.3389/fpsyg.2017.01849
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author de Haan-Rietdijk, Silvia
Voelkle, Manuel C.
Keijsers, Loes
Hamaker, Ellen L.
author_facet de Haan-Rietdijk, Silvia
Voelkle, Manuel C.
Keijsers, Loes
Hamaker, Ellen L.
author_sort de Haan-Rietdijk, Silvia
collection PubMed
description The Experience Sampling Method is a common approach in psychological research for collecting intensive longitudinal data with high ecological validity. One characteristic of ESM data is that it is often unequally spaced, because the measurement intervals within a day are deliberately varied, and measurement continues over several days. This poses a problem for discrete-time (DT) modeling approaches, which are based on the assumption that all measurements are equally spaced. Nevertheless, DT approaches such as (vector) autoregressive modeling are often used to analyze ESM data, for instance in the context of affective dynamics research. There are equivalent continuous-time (CT) models, but they are more difficult to implement. In this paper we take a pragmatic approach and evaluate the practical relevance of the violated model assumption in DT AR(1) and VAR(1) models, for the N = 1 case. We use simulated data under an ESM measurement design to investigate the bias in the parameters of interest under four different model implementations, ranging from the true CT model that accounts for all the exact measurement times, to the crudest possible DT model implementation, where even the nighttime is treated as a regular interval. An analysis of empirical affect data illustrates how the differences between DT and CT modeling can play out in practice. We find that the size and the direction of the bias in DT (V)AR models for unequally spaced ESM data depend quite strongly on the true parameter in addition to data characteristics. Our recommendation is to use CT modeling whenever possible, especially now that new software implementations have become available.
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spelling pubmed-56550342017-11-03 Discrete- vs. Continuous-Time Modeling of Unequally Spaced Experience Sampling Method Data de Haan-Rietdijk, Silvia Voelkle, Manuel C. Keijsers, Loes Hamaker, Ellen L. Front Psychol Psychology The Experience Sampling Method is a common approach in psychological research for collecting intensive longitudinal data with high ecological validity. One characteristic of ESM data is that it is often unequally spaced, because the measurement intervals within a day are deliberately varied, and measurement continues over several days. This poses a problem for discrete-time (DT) modeling approaches, which are based on the assumption that all measurements are equally spaced. Nevertheless, DT approaches such as (vector) autoregressive modeling are often used to analyze ESM data, for instance in the context of affective dynamics research. There are equivalent continuous-time (CT) models, but they are more difficult to implement. In this paper we take a pragmatic approach and evaluate the practical relevance of the violated model assumption in DT AR(1) and VAR(1) models, for the N = 1 case. We use simulated data under an ESM measurement design to investigate the bias in the parameters of interest under four different model implementations, ranging from the true CT model that accounts for all the exact measurement times, to the crudest possible DT model implementation, where even the nighttime is treated as a regular interval. An analysis of empirical affect data illustrates how the differences between DT and CT modeling can play out in practice. We find that the size and the direction of the bias in DT (V)AR models for unequally spaced ESM data depend quite strongly on the true parameter in addition to data characteristics. Our recommendation is to use CT modeling whenever possible, especially now that new software implementations have become available. Frontiers Media S.A. 2017-10-20 /pmc/articles/PMC5655034/ /pubmed/29104554 http://dx.doi.org/10.3389/fpsyg.2017.01849 Text en Copyright © 2017 de Haan-Rietdijk, Voelkle, Keijsers and Hamaker. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychology
de Haan-Rietdijk, Silvia
Voelkle, Manuel C.
Keijsers, Loes
Hamaker, Ellen L.
Discrete- vs. Continuous-Time Modeling of Unequally Spaced Experience Sampling Method Data
title Discrete- vs. Continuous-Time Modeling of Unequally Spaced Experience Sampling Method Data
title_full Discrete- vs. Continuous-Time Modeling of Unequally Spaced Experience Sampling Method Data
title_fullStr Discrete- vs. Continuous-Time Modeling of Unequally Spaced Experience Sampling Method Data
title_full_unstemmed Discrete- vs. Continuous-Time Modeling of Unequally Spaced Experience Sampling Method Data
title_short Discrete- vs. Continuous-Time Modeling of Unequally Spaced Experience Sampling Method Data
title_sort discrete- vs. continuous-time modeling of unequally spaced experience sampling method data
topic Psychology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655034/
https://www.ncbi.nlm.nih.gov/pubmed/29104554
http://dx.doi.org/10.3389/fpsyg.2017.01849
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