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Power considerations for the application of detrended fluctuation analysis in gait variability studies

The assessment of gait variability using stochastic signal processing techniques such as detrended fluctuation analysis (DFA) has been shown to be a sensitive tool for evaluation of gait alterations due to aging and neuromuscular disease. However, previous studies have suggested that the application...

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Autores principales: Kuznetsov, Nikita A., Rhea, Christopher K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360325/
https://www.ncbi.nlm.nih.gov/pubmed/28323871
http://dx.doi.org/10.1371/journal.pone.0174144
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author Kuznetsov, Nikita A.
Rhea, Christopher K.
author_facet Kuznetsov, Nikita A.
Rhea, Christopher K.
author_sort Kuznetsov, Nikita A.
collection PubMed
description The assessment of gait variability using stochastic signal processing techniques such as detrended fluctuation analysis (DFA) has been shown to be a sensitive tool for evaluation of gait alterations due to aging and neuromuscular disease. However, previous studies have suggested that the application of DFA requires relatively long recordings (600 strides), which is difficult when working with clinical populations or older adults. In this paper we propose a model for predicting DFA variance in experimental data and conduct a Monte Carlo simulation to estimate the sample size and number of trials required to detect a change in DFA scaling exponent. We illustrate the model in a simulation to detect a difference of 0.1 (medium effect) between two groups of subjects when using short gait time series (100 to 200 strides) in the context of between- and within-subject designs. We assumed that the variance of DFA scaling exponent arises due to individual differences, time series length, and experimental error. Results showed that sample sizes required to achieve acceptable power of 80% are practically feasible, especially when using within-subject designs. For example, to detect a group difference in the DFA scaling exponent of 0.1, it would require either 25 subjects and 2 trials per subject or 12 subjects and 4 trials per subject using a within-subject design. We then compared plausibility of such power predictions to the empirically observed power from a study that required subjects to synchronize with a persistent fractal metronome. The results showed that the model adequately predicted the empirical pattern of results. Our power simulations could be used in conjunction with previous design guidelines in the literature when planning new gait variability experiments.
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spelling pubmed-53603252017-04-06 Power considerations for the application of detrended fluctuation analysis in gait variability studies Kuznetsov, Nikita A. Rhea, Christopher K. PLoS One Research Article The assessment of gait variability using stochastic signal processing techniques such as detrended fluctuation analysis (DFA) has been shown to be a sensitive tool for evaluation of gait alterations due to aging and neuromuscular disease. However, previous studies have suggested that the application of DFA requires relatively long recordings (600 strides), which is difficult when working with clinical populations or older adults. In this paper we propose a model for predicting DFA variance in experimental data and conduct a Monte Carlo simulation to estimate the sample size and number of trials required to detect a change in DFA scaling exponent. We illustrate the model in a simulation to detect a difference of 0.1 (medium effect) between two groups of subjects when using short gait time series (100 to 200 strides) in the context of between- and within-subject designs. We assumed that the variance of DFA scaling exponent arises due to individual differences, time series length, and experimental error. Results showed that sample sizes required to achieve acceptable power of 80% are practically feasible, especially when using within-subject designs. For example, to detect a group difference in the DFA scaling exponent of 0.1, it would require either 25 subjects and 2 trials per subject or 12 subjects and 4 trials per subject using a within-subject design. We then compared plausibility of such power predictions to the empirically observed power from a study that required subjects to synchronize with a persistent fractal metronome. The results showed that the model adequately predicted the empirical pattern of results. Our power simulations could be used in conjunction with previous design guidelines in the literature when planning new gait variability experiments. Public Library of Science 2017-03-21 /pmc/articles/PMC5360325/ /pubmed/28323871 http://dx.doi.org/10.1371/journal.pone.0174144 Text en © 2017 Kuznetsov, Rhea http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kuznetsov, Nikita A.
Rhea, Christopher K.
Power considerations for the application of detrended fluctuation analysis in gait variability studies
title Power considerations for the application of detrended fluctuation analysis in gait variability studies
title_full Power considerations for the application of detrended fluctuation analysis in gait variability studies
title_fullStr Power considerations for the application of detrended fluctuation analysis in gait variability studies
title_full_unstemmed Power considerations for the application of detrended fluctuation analysis in gait variability studies
title_short Power considerations for the application of detrended fluctuation analysis in gait variability studies
title_sort power considerations for the application of detrended fluctuation analysis in gait variability studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360325/
https://www.ncbi.nlm.nih.gov/pubmed/28323871
http://dx.doi.org/10.1371/journal.pone.0174144
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