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Empirical Priors in Polytomous Computerized Adaptive Tests: Risks and Rewards in Clinical Settings
The use of empirical prior information about participants has been shown to substantially improve the efficiency of computerized adaptive tests (CATs) in educational settings. However, it is unclear how these results translate to clinical settings, where small item banks with highly informative poly...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679926/ https://www.ncbi.nlm.nih.gov/pubmed/36425285 http://dx.doi.org/10.1177/01466216221124091 |
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author | Frans, Niek Braeken, Johan Veldkamp, Bernard P. Paap, Muirne C. S. |
author_facet | Frans, Niek Braeken, Johan Veldkamp, Bernard P. Paap, Muirne C. S. |
author_sort | Frans, Niek |
collection | PubMed |
description | The use of empirical prior information about participants has been shown to substantially improve the efficiency of computerized adaptive tests (CATs) in educational settings. However, it is unclear how these results translate to clinical settings, where small item banks with highly informative polytomous items often lead to very short CATs. We explored the risks and rewards of using prior information in CAT in two simulation studies, rooted in applied clinical examples. In the first simulation, prior precision and bias in the prior location were manipulated independently. Our results show that a precise personalized prior can meaningfully increase CAT efficiency. However, this reward comes with the potential risk of overconfidence in wrong empirical information (i.e., using a precise severely biased prior), which can lead to unnecessarily long tests, or severely biased estimates. The latter risk can be mitigated by setting a minimum number of items that are to be administered during the CAT, or by setting a less precise prior; be it at the expense of canceling out any efficiency gains. The second simulation, with more realistic bias and precision combinations in the empirical prior, places the prevalence of the potential risks in context. With similar estimation bias, an empirical prior reduced CAT test length, compared to a standard normal prior, in 68% of cases, by a median of 20%; while test length increased in only 3% of cases. The use of prior information in CAT seems to be a feasible and simple method to reduce test burden for patients and clinical practitioners alike. |
format | Online Article Text |
id | pubmed-9679926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-96799262022-11-23 Empirical Priors in Polytomous Computerized Adaptive Tests: Risks and Rewards in Clinical Settings Frans, Niek Braeken, Johan Veldkamp, Bernard P. Paap, Muirne C. S. Appl Psychol Meas Articles The use of empirical prior information about participants has been shown to substantially improve the efficiency of computerized adaptive tests (CATs) in educational settings. However, it is unclear how these results translate to clinical settings, where small item banks with highly informative polytomous items often lead to very short CATs. We explored the risks and rewards of using prior information in CAT in two simulation studies, rooted in applied clinical examples. In the first simulation, prior precision and bias in the prior location were manipulated independently. Our results show that a precise personalized prior can meaningfully increase CAT efficiency. However, this reward comes with the potential risk of overconfidence in wrong empirical information (i.e., using a precise severely biased prior), which can lead to unnecessarily long tests, or severely biased estimates. The latter risk can be mitigated by setting a minimum number of items that are to be administered during the CAT, or by setting a less precise prior; be it at the expense of canceling out any efficiency gains. The second simulation, with more realistic bias and precision combinations in the empirical prior, places the prevalence of the potential risks in context. With similar estimation bias, an empirical prior reduced CAT test length, compared to a standard normal prior, in 68% of cases, by a median of 20%; while test length increased in only 3% of cases. The use of prior information in CAT seems to be a feasible and simple method to reduce test burden for patients and clinical practitioners alike. SAGE Publications 2022-09-30 2023-01 /pmc/articles/PMC9679926/ /pubmed/36425285 http://dx.doi.org/10.1177/01466216221124091 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Articles Frans, Niek Braeken, Johan Veldkamp, Bernard P. Paap, Muirne C. S. Empirical Priors in Polytomous Computerized Adaptive Tests: Risks and Rewards in Clinical Settings |
title | Empirical Priors in Polytomous Computerized Adaptive Tests: Risks and
Rewards in Clinical Settings |
title_full | Empirical Priors in Polytomous Computerized Adaptive Tests: Risks and
Rewards in Clinical Settings |
title_fullStr | Empirical Priors in Polytomous Computerized Adaptive Tests: Risks and
Rewards in Clinical Settings |
title_full_unstemmed | Empirical Priors in Polytomous Computerized Adaptive Tests: Risks and
Rewards in Clinical Settings |
title_short | Empirical Priors in Polytomous Computerized Adaptive Tests: Risks and
Rewards in Clinical Settings |
title_sort | empirical priors in polytomous computerized adaptive tests: risks and
rewards in clinical settings |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679926/ https://www.ncbi.nlm.nih.gov/pubmed/36425285 http://dx.doi.org/10.1177/01466216221124091 |
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