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      Trajectory Modelling Techniques Useful to Epidemiological Research: A Comparative Narrative Review of Approaches

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          Abstract

          Trajectory modelling techniques have been developed to determine subgroups within a given population and are increasingly used to better understand intra- and inter-individual variability in health outcome patterns over time. The objectives of this narrative review are to explore various trajectory modelling approaches useful to epidemiological research and give an overview of their applications and differences. Guidance for reporting on the results of trajectory modelling is also covered. Trajectory modelling techniques reviewed include latent class modelling approaches, ie, growth mixture modelling (GMM), group-based trajectory modelling (GBTM), latent class analysis (LCA), and latent transition analysis (LTA). A parallel is drawn to other individual-centered statistical approaches such as cluster analysis (CA) and sequence analysis (SA). Depending on the research question and type of data, a number of approaches can be used for trajectory modelling of health outcomes measured in longitudinal studies. However, the various terms to designate latent class modelling approaches (GMM, GBTM, LTA, LCA) are used inconsistently and often interchangeably in the available scientific literature. Improved consistency in the terminology and reporting guidelines have the potential to increase researchers’ efficiency when it comes to choosing the most appropriate technique that best suits their research questions.

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          Group-based trajectory modeling in clinical research.

          Group-based trajectory models are increasingly being applied in clinical research to map the developmental course of symptoms and assess heterogeneity in response to clinical interventions. In this review, we provide a nontechnical overview of group-based trajectory and growth mixture modeling alongside a sampling of how these models have been applied in clinical research. We discuss the challenges associated with the application of both types of group-based models and propose a set of preliminary guidelines for applied researchers to follow when reporting model results. Future directions in group-based modeling applications are discussed, including the use of trajectory models to facilitate causal inference when random assignment to treatment condition is not possible.
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            Auxiliary Variables in Mixture Modeling: Three-Step Approaches Using Mplus

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              How to Use a Monte Carlo Study to Decide on Sample Size and Determine Power

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                Author and article information

                Journal
                Clin Epidemiol
                Clin Epidemiol
                clep
                clinepid
                Clinical Epidemiology
                Dove
                1179-1349
                30 October 2020
                2020
                : 12
                : 1205-1222
                Affiliations
                [1 ]Département des Sciences de la santé, Université du Québec en Abitibi-Témiscamingue (UQAT) , Rouyn-Noranda, Québec, Canada
                [2 ]Centre de Recherche du Centre Hospitalier de l’Université de Montréal (CRCHUM) , Montréal, Québec, Canada
                [3 ]Département d’anesthésiologie et de médecine de la douleur, Faculté de médecine, Université de Montréal , Montréal, Québec, Canada
                [4 ]Department of Psychology, Faculty of Health, York University , Toronto, Ontario, Canada
                [5 ]Département de médecine de famille et de médecine d’urgence, Faculté de médecine et des sciences de la santé, Université de Sherbrooke , Sherbrooke, Québec, Canada
                [6 ]Centre de recherche du Centre hospitalier Universitaire de Sherbrooke (CRCHUS) , Sherbrooke, Québec, Canada
                [7 ]StatSciences Inc., Notre-Dame-de-lL’île-Perrot , Québec, Canada
                Author notes
                Correspondence: Anaïs Lacasse Département des sciences de la santé, Université du Québec en Abitibi-Témiscamingue (UQAT), 445, Boul. de l’Université , Rouyn-Noranda (Qc)J9X 5E4, Québec, CanadaTel +1 819 762 0971, 2722 Email lacassea@uqat.ca
                Author information
                http://orcid.org/0000-0002-7742-2717
                http://orcid.org/0000-0002-8686-447X
                http://orcid.org/0000-0001-9593-8883
                Article
                265287
                10.2147/CLEP.S265287
                7608582
                33154677
                3ce2f646-ac7f-4789-8348-cbf94a882a87
                © 2020 Nguena Nguefack et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 30 May 2020
                : 22 September 2020
                Page count
                Figures: 1, Tables: 3, References: 139, Pages: 18
                Categories
                Review

                Public health
                modelling techniques,growth mixture modelling,group-based trajectory modelling,latent class analysis,latent transition analysis,cluster analysis,sequence analysis

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