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Dyslexia treatment studies: A systematic review and suggestions on testing treatment efficacy with small effects and small samples
Poor response to treatment is a defining characteristic of reading disorder. In the present systematic review and meta-analysis, we found that the overall average effect size for treatment efficacy was modest, with a mean standardized difference of 0.38. Small true effects, combined with the difficu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516770/ https://www.ncbi.nlm.nih.gov/pubmed/33694077 http://dx.doi.org/10.3758/s13428-021-01549-x |
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author | Toffalini, Enrico Giofrè, David Pastore, Massimiliano Carretti, Barbara Fraccadori, Federica Szűcs, Denes |
author_facet | Toffalini, Enrico Giofrè, David Pastore, Massimiliano Carretti, Barbara Fraccadori, Federica Szűcs, Denes |
author_sort | Toffalini, Enrico |
collection | PubMed |
description | Poor response to treatment is a defining characteristic of reading disorder. In the present systematic review and meta-analysis, we found that the overall average effect size for treatment efficacy was modest, with a mean standardized difference of 0.38. Small true effects, combined with the difficulty to recruit large samples, seriously challenge researchers planning to test treatment efficacy in dyslexia and potentially in other learning disorders. Nonetheless, most published studies claim effectiveness, generally based on liberal use of multiple testing. This inflates the risk that most statistically significant results are associated with overestimated effect sizes. To enhance power, we propose the strategic use of repeated measurements with mixed-effects modelling. This novel approach would enable us to estimate both individual parameters and population-level effects more reliably. We suggest assessing a reading outcome not once, but three times, at pre-treatment and three times at post-treatment. Such design would require only modest additional efforts compared to current practices. Based on this, we performed ad hoc a priori design analyses via simulation studies. Results showed that using the novel design may allow one to reach adequate power even with low sample sizes of 30–40 participants (i.e., 15–20 participants per group) for a typical effect size of d = 0.38. Nonetheless, more conservative assumptions are warranted for various reasons, including a high risk of publication bias in the extant literature. Our considerations can be extended to intervention studies of other types of neurodevelopmental disorders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.3758/s13428-021-01549-x. |
format | Online Article Text |
id | pubmed-8516770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-85167702021-10-29 Dyslexia treatment studies: A systematic review and suggestions on testing treatment efficacy with small effects and small samples Toffalini, Enrico Giofrè, David Pastore, Massimiliano Carretti, Barbara Fraccadori, Federica Szűcs, Denes Behav Res Methods Article Poor response to treatment is a defining characteristic of reading disorder. In the present systematic review and meta-analysis, we found that the overall average effect size for treatment efficacy was modest, with a mean standardized difference of 0.38. Small true effects, combined with the difficulty to recruit large samples, seriously challenge researchers planning to test treatment efficacy in dyslexia and potentially in other learning disorders. Nonetheless, most published studies claim effectiveness, generally based on liberal use of multiple testing. This inflates the risk that most statistically significant results are associated with overestimated effect sizes. To enhance power, we propose the strategic use of repeated measurements with mixed-effects modelling. This novel approach would enable us to estimate both individual parameters and population-level effects more reliably. We suggest assessing a reading outcome not once, but three times, at pre-treatment and three times at post-treatment. Such design would require only modest additional efforts compared to current practices. Based on this, we performed ad hoc a priori design analyses via simulation studies. Results showed that using the novel design may allow one to reach adequate power even with low sample sizes of 30–40 participants (i.e., 15–20 participants per group) for a typical effect size of d = 0.38. Nonetheless, more conservative assumptions are warranted for various reasons, including a high risk of publication bias in the extant literature. Our considerations can be extended to intervention studies of other types of neurodevelopmental disorders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.3758/s13428-021-01549-x. Springer US 2021-03-10 2021 /pmc/articles/PMC8516770/ /pubmed/33694077 http://dx.doi.org/10.3758/s13428-021-01549-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Toffalini, Enrico Giofrè, David Pastore, Massimiliano Carretti, Barbara Fraccadori, Federica Szűcs, Denes Dyslexia treatment studies: A systematic review and suggestions on testing treatment efficacy with small effects and small samples |
title | Dyslexia treatment studies: A systematic review and suggestions on testing treatment efficacy with small effects and small samples |
title_full | Dyslexia treatment studies: A systematic review and suggestions on testing treatment efficacy with small effects and small samples |
title_fullStr | Dyslexia treatment studies: A systematic review and suggestions on testing treatment efficacy with small effects and small samples |
title_full_unstemmed | Dyslexia treatment studies: A systematic review and suggestions on testing treatment efficacy with small effects and small samples |
title_short | Dyslexia treatment studies: A systematic review and suggestions on testing treatment efficacy with small effects and small samples |
title_sort | dyslexia treatment studies: a systematic review and suggestions on testing treatment efficacy with small effects and small samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516770/ https://www.ncbi.nlm.nih.gov/pubmed/33694077 http://dx.doi.org/10.3758/s13428-021-01549-x |
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