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The correlation between baseline score and post-intervention score, and its implications for statistical analysis

BACKGROUND: When using a continuous outcome measure in a randomised controlled trial (RCT), the baseline score should be measured in addition to the post-intervention score, and it should be analysed using the appropriate statistical analysis. METHODS: We derive the correlation between the change sc...

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Autores principales: Clifton, Lei, Clifton, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330413/
https://www.ncbi.nlm.nih.gov/pubmed/30635021
http://dx.doi.org/10.1186/s13063-018-3108-3
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author Clifton, Lei
Clifton, David A.
author_facet Clifton, Lei
Clifton, David A.
author_sort Clifton, Lei
collection PubMed
description BACKGROUND: When using a continuous outcome measure in a randomised controlled trial (RCT), the baseline score should be measured in addition to the post-intervention score, and it should be analysed using the appropriate statistical analysis. METHODS: We derive the correlation between the change score and baseline score and show that there is always a correlation (usually negative) between the change score and baseline score. We discuss the following correlations and provide the mathematical derivations in the Appendix: Correlation between change score and baseline score. Correlation between change score and post score. Correlation between change score and average score. The setting here is a parallel, two-arm RCT, but the method discussed in this paper is applicable for any studies or trials that have a continuous outcome measure; it is not restricted to RCTs. RESULTS: We show that using the change score as the outcome measure does not address the problem of regression to the mean, nor does it take account of the baseline imbalance. Whether the outcome is change score or post score, one should always adjust for baseline using analysis of covariance (ANCOVA); otherwise, the estimated treat effect may be biased. We show that these correlations also apply when comparing two measurement methods using Bland-Altman plots. CONCLUSIONS: The correlation between baseline and post-intervention scores can be derived using the variance sum law. We can then use the derived correlation to calculate the required sample size in the design stage. Baseline imbalance may occur in RCTs, and ANCOVA should be used to adjust for baseline in the analysis stage.
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spelling pubmed-63304132019-01-16 The correlation between baseline score and post-intervention score, and its implications for statistical analysis Clifton, Lei Clifton, David A. Trials Methodology BACKGROUND: When using a continuous outcome measure in a randomised controlled trial (RCT), the baseline score should be measured in addition to the post-intervention score, and it should be analysed using the appropriate statistical analysis. METHODS: We derive the correlation between the change score and baseline score and show that there is always a correlation (usually negative) between the change score and baseline score. We discuss the following correlations and provide the mathematical derivations in the Appendix: Correlation between change score and baseline score. Correlation between change score and post score. Correlation between change score and average score. The setting here is a parallel, two-arm RCT, but the method discussed in this paper is applicable for any studies or trials that have a continuous outcome measure; it is not restricted to RCTs. RESULTS: We show that using the change score as the outcome measure does not address the problem of regression to the mean, nor does it take account of the baseline imbalance. Whether the outcome is change score or post score, one should always adjust for baseline using analysis of covariance (ANCOVA); otherwise, the estimated treat effect may be biased. We show that these correlations also apply when comparing two measurement methods using Bland-Altman plots. CONCLUSIONS: The correlation between baseline and post-intervention scores can be derived using the variance sum law. We can then use the derived correlation to calculate the required sample size in the design stage. Baseline imbalance may occur in RCTs, and ANCOVA should be used to adjust for baseline in the analysis stage. BioMed Central 2019-01-11 /pmc/articles/PMC6330413/ /pubmed/30635021 http://dx.doi.org/10.1186/s13063-018-3108-3 Text en © The Author(s). 2019 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 Methodology
Clifton, Lei
Clifton, David A.
The correlation between baseline score and post-intervention score, and its implications for statistical analysis
title The correlation between baseline score and post-intervention score, and its implications for statistical analysis
title_full The correlation between baseline score and post-intervention score, and its implications for statistical analysis
title_fullStr The correlation between baseline score and post-intervention score, and its implications for statistical analysis
title_full_unstemmed The correlation between baseline score and post-intervention score, and its implications for statistical analysis
title_short The correlation between baseline score and post-intervention score, and its implications for statistical analysis
title_sort correlation between baseline score and post-intervention score, and its implications for statistical analysis
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330413/
https://www.ncbi.nlm.nih.gov/pubmed/30635021
http://dx.doi.org/10.1186/s13063-018-3108-3
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