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Modified interactive Q-learning for attenuating the impact of model misspecification with treatment effect heterogeneity
A sequential multiple assignment randomized trial, which incorporates multiple stages of randomization, is a popular approach for collecting data to inform personalized and adaptive treatments. There is an extensive literature on statistical methods to analyze data collected in sequential multiple a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683339/ https://www.ncbi.nlm.nih.gov/pubmed/37859598 http://dx.doi.org/10.1177/09622802231206471 |
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author | Zhang, Yuan Vock, David M Patrick, Megan E Murray, Thomas A |
author_facet | Zhang, Yuan Vock, David M Patrick, Megan E Murray, Thomas A |
author_sort | Zhang, Yuan |
collection | PubMed |
description | A sequential multiple assignment randomized trial, which incorporates multiple stages of randomization, is a popular approach for collecting data to inform personalized and adaptive treatments. There is an extensive literature on statistical methods to analyze data collected in sequential multiple assignment randomized trials and estimate the optimal dynamic treatment regime. Q-learning with linear regression is widely used for this purpose due to its ease of implementation. However, model misspecification is a common problem with this approach, and little attention has been given to the impact of model misspecification when treatment effects are heterogeneous across subjects. This article describes the integrative impact of two possible types of model misspecification related to treatment effect heterogeneity: omitted early-stage treatment effects in late-stage main effect model, and violated linearity assumption between pseudo-outcomes and predictors despite non-linearity arising from the optimization operation. The proposed method, aiming to deal with both types of misspecification concomitantly, builds interactive models into modified parametric Q-learning with Murphy’s regret function. Simulations show that the proposed method is robust to both sources of model misspecification. The proposed method is applied to a two-stage sequential multiple assignment randomized trial with embedded tailoring aimed at reducing binge drinking in first-year college students. |
format | Online Article Text |
id | pubmed-10683339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-106833392023-11-30 Modified interactive Q-learning for attenuating the impact of model misspecification with treatment effect heterogeneity Zhang, Yuan Vock, David M Patrick, Megan E Murray, Thomas A Stat Methods Med Res Original Research Articles A sequential multiple assignment randomized trial, which incorporates multiple stages of randomization, is a popular approach for collecting data to inform personalized and adaptive treatments. There is an extensive literature on statistical methods to analyze data collected in sequential multiple assignment randomized trials and estimate the optimal dynamic treatment regime. Q-learning with linear regression is widely used for this purpose due to its ease of implementation. However, model misspecification is a common problem with this approach, and little attention has been given to the impact of model misspecification when treatment effects are heterogeneous across subjects. This article describes the integrative impact of two possible types of model misspecification related to treatment effect heterogeneity: omitted early-stage treatment effects in late-stage main effect model, and violated linearity assumption between pseudo-outcomes and predictors despite non-linearity arising from the optimization operation. The proposed method, aiming to deal with both types of misspecification concomitantly, builds interactive models into modified parametric Q-learning with Murphy’s regret function. Simulations show that the proposed method is robust to both sources of model misspecification. The proposed method is applied to a two-stage sequential multiple assignment randomized trial with embedded tailoring aimed at reducing binge drinking in first-year college students. SAGE Publications 2023-10-20 2023-11 /pmc/articles/PMC10683339/ /pubmed/37859598 http://dx.doi.org/10.1177/09622802231206471 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any 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 | Original Research Articles Zhang, Yuan Vock, David M Patrick, Megan E Murray, Thomas A Modified interactive Q-learning for attenuating the impact of model misspecification with treatment effect heterogeneity |
title | Modified interactive Q-learning for attenuating the impact of model misspecification with treatment effect heterogeneity |
title_full | Modified interactive Q-learning for attenuating the impact of model misspecification with treatment effect heterogeneity |
title_fullStr | Modified interactive Q-learning for attenuating the impact of model misspecification with treatment effect heterogeneity |
title_full_unstemmed | Modified interactive Q-learning for attenuating the impact of model misspecification with treatment effect heterogeneity |
title_short | Modified interactive Q-learning for attenuating the impact of model misspecification with treatment effect heterogeneity |
title_sort | modified interactive q-learning for attenuating the impact of model misspecification with treatment effect heterogeneity |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683339/ https://www.ncbi.nlm.nih.gov/pubmed/37859598 http://dx.doi.org/10.1177/09622802231206471 |
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