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A simple ratio-based approach for power and sample size determination for 2-group comparison using Rasch models

BACKGROUND: Despite the widespread use of patient-reported Outcomes (PRO) in clinical studies, their design remains a challenge. Justification of study size is hardly provided, especially when a Rasch model is planned for analysing the data in a 2-group comparison study. The classical sample size fo...

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Autores principales: Sébille, Véronique, Blanchin, Myriam, Guillemin, Francis, Falissard, Bruno, Hardouin, Jean-Benoit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105835/
https://www.ncbi.nlm.nih.gov/pubmed/24996957
http://dx.doi.org/10.1186/1471-2288-14-87
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author Sébille, Véronique
Blanchin, Myriam
Guillemin, Francis
Falissard, Bruno
Hardouin, Jean-Benoit
author_facet Sébille, Véronique
Blanchin, Myriam
Guillemin, Francis
Falissard, Bruno
Hardouin, Jean-Benoit
author_sort Sébille, Véronique
collection PubMed
description BACKGROUND: Despite the widespread use of patient-reported Outcomes (PRO) in clinical studies, their design remains a challenge. Justification of study size is hardly provided, especially when a Rasch model is planned for analysing the data in a 2-group comparison study. The classical sample size formula (CLASSIC) for comparing normally distributed endpoints between two groups has shown to be inadequate in this setting (underestimated study sizes). A correction factor (RATIO) has been proposed to reach an adequate sample size from the CLASSIC when a Rasch model is intended to be used for analysis. The objective was to explore the impact of the parameters used for study design on the RATIO and to identify the most relevant to provide a simple method for sample size determination for Rasch modelling. METHODS: A large combination of parameters used for study design was simulated using a Monte Carlo method: variance of the latent trait, group effect, sample size per group, number of items and items difficulty parameters. A linear regression model explaining the RATIO and including all the former parameters as covariates was fitted. RESULTS: The most relevant parameters explaining the ratio’s variations were the number of items and the variance of the latent trait (R(2) = 99.4%). CONCLUSIONS: Using the classical sample size formula adjusted with the proposed RATIO can provide a straightforward and reliable formula for sample size computation for 2-group comparison of PRO data using Rasch models.
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spelling pubmed-41058352014-08-04 A simple ratio-based approach for power and sample size determination for 2-group comparison using Rasch models Sébille, Véronique Blanchin, Myriam Guillemin, Francis Falissard, Bruno Hardouin, Jean-Benoit BMC Med Res Methodol Research Article BACKGROUND: Despite the widespread use of patient-reported Outcomes (PRO) in clinical studies, their design remains a challenge. Justification of study size is hardly provided, especially when a Rasch model is planned for analysing the data in a 2-group comparison study. The classical sample size formula (CLASSIC) for comparing normally distributed endpoints between two groups has shown to be inadequate in this setting (underestimated study sizes). A correction factor (RATIO) has been proposed to reach an adequate sample size from the CLASSIC when a Rasch model is intended to be used for analysis. The objective was to explore the impact of the parameters used for study design on the RATIO and to identify the most relevant to provide a simple method for sample size determination for Rasch modelling. METHODS: A large combination of parameters used for study design was simulated using a Monte Carlo method: variance of the latent trait, group effect, sample size per group, number of items and items difficulty parameters. A linear regression model explaining the RATIO and including all the former parameters as covariates was fitted. RESULTS: The most relevant parameters explaining the ratio’s variations were the number of items and the variance of the latent trait (R(2) = 99.4%). CONCLUSIONS: Using the classical sample size formula adjusted with the proposed RATIO can provide a straightforward and reliable formula for sample size computation for 2-group comparison of PRO data using Rasch models. BioMed Central 2014-07-05 /pmc/articles/PMC4105835/ /pubmed/24996957 http://dx.doi.org/10.1186/1471-2288-14-87 Text en Copyright © 2014 Sébille et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sébille, Véronique
Blanchin, Myriam
Guillemin, Francis
Falissard, Bruno
Hardouin, Jean-Benoit
A simple ratio-based approach for power and sample size determination for 2-group comparison using Rasch models
title A simple ratio-based approach for power and sample size determination for 2-group comparison using Rasch models
title_full A simple ratio-based approach for power and sample size determination for 2-group comparison using Rasch models
title_fullStr A simple ratio-based approach for power and sample size determination for 2-group comparison using Rasch models
title_full_unstemmed A simple ratio-based approach for power and sample size determination for 2-group comparison using Rasch models
title_short A simple ratio-based approach for power and sample size determination for 2-group comparison using Rasch models
title_sort simple ratio-based approach for power and sample size determination for 2-group comparison using rasch models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105835/
https://www.ncbi.nlm.nih.gov/pubmed/24996957
http://dx.doi.org/10.1186/1471-2288-14-87
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