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Correcting the predictive validity of a selection test for the effect of indirect range restriction
BACKGROUND: The validity of selection tests is underestimated if it is determined by simply calculating the predictor-outcome correlation found in the admitted group. This correlation is usually attenuated by two factors: (1) the combination of selection variables which can compensate for each other...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725878/ https://www.ncbi.nlm.nih.gov/pubmed/29228995 http://dx.doi.org/10.1186/s12909-017-1070-5 |
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author | Zimmermann, Stefan Klusmann, Dietrich Hampe, Wolfgang |
author_facet | Zimmermann, Stefan Klusmann, Dietrich Hampe, Wolfgang |
author_sort | Zimmermann, Stefan |
collection | PubMed |
description | BACKGROUND: The validity of selection tests is underestimated if it is determined by simply calculating the predictor-outcome correlation found in the admitted group. This correlation is usually attenuated by two factors: (1) the combination of selection variables which can compensate for each other and (2) range restriction in predictor and outcome due to the absence of outcome measures for rejected applicants. METHODS: Here we demonstrate the logic of these artifacts in a situation typical for student selection tests and compare four different methods for their correction: two formulas for the correction of direct and indirect range restriction, expectation maximization algorithm (EM) and multiple imputation by chained equations (MICE). First we show with simulated data how a realistic estimation of predictive validity could be achieved; second we apply the same methods to empirical data from one medical school. RESULTS: The results of the four methods are very similar except for the direct range restriction formula which underestimated validity. CONCLUSION: For practical purposes Thorndike’s case C formula is a relatively straightforward solution to the range restriction problem, provided distributional assumptions are met. With EM and MICE more precision is obtained when distributional requirements are not met, but access to a sophisticated statistical package such as R is needed. The use of true score correlation has its own problems and does not seem to provide a better correction than other methods. |
format | Online Article Text |
id | pubmed-5725878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57258782017-12-13 Correcting the predictive validity of a selection test for the effect of indirect range restriction Zimmermann, Stefan Klusmann, Dietrich Hampe, Wolfgang BMC Med Educ Research Article BACKGROUND: The validity of selection tests is underestimated if it is determined by simply calculating the predictor-outcome correlation found in the admitted group. This correlation is usually attenuated by two factors: (1) the combination of selection variables which can compensate for each other and (2) range restriction in predictor and outcome due to the absence of outcome measures for rejected applicants. METHODS: Here we demonstrate the logic of these artifacts in a situation typical for student selection tests and compare four different methods for their correction: two formulas for the correction of direct and indirect range restriction, expectation maximization algorithm (EM) and multiple imputation by chained equations (MICE). First we show with simulated data how a realistic estimation of predictive validity could be achieved; second we apply the same methods to empirical data from one medical school. RESULTS: The results of the four methods are very similar except for the direct range restriction formula which underestimated validity. CONCLUSION: For practical purposes Thorndike’s case C formula is a relatively straightforward solution to the range restriction problem, provided distributional assumptions are met. With EM and MICE more precision is obtained when distributional requirements are not met, but access to a sophisticated statistical package such as R is needed. The use of true score correlation has its own problems and does not seem to provide a better correction than other methods. BioMed Central 2017-12-11 /pmc/articles/PMC5725878/ /pubmed/29228995 http://dx.doi.org/10.1186/s12909-017-1070-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Zimmermann, Stefan Klusmann, Dietrich Hampe, Wolfgang Correcting the predictive validity of a selection test for the effect of indirect range restriction |
title | Correcting the predictive validity of a selection test for the effect of indirect range restriction |
title_full | Correcting the predictive validity of a selection test for the effect of indirect range restriction |
title_fullStr | Correcting the predictive validity of a selection test for the effect of indirect range restriction |
title_full_unstemmed | Correcting the predictive validity of a selection test for the effect of indirect range restriction |
title_short | Correcting the predictive validity of a selection test for the effect of indirect range restriction |
title_sort | correcting the predictive validity of a selection test for the effect of indirect range restriction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725878/ https://www.ncbi.nlm.nih.gov/pubmed/29228995 http://dx.doi.org/10.1186/s12909-017-1070-5 |
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