1,721,007 research outputs found

    An Unconditional Test for Change Point Detection in Binary Sequences with Applications to Clinical Registries

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    Objectives: Methods for change point (also sometimes referred to as threshold or breakpoint) detection in binary sequences are not new and were introduced as early as 1955. Much of the research in this area has focussed on asymptotic and exact conditional methods. Here we develop an exact unconditional test. Methods: An unconditional exact test is developed which assumes the total number of events as random instead of conditioning on the number of observed events. The new test is shown to be uniformly more powerful than Worsley's exact conditional test and means for its efficient numerical calculations are given. Adaptions of methods by Berger and Boos are made to deal with the issue that the unknown event probability imposes a nuisance parameter. The methods are compared in a Monte Carlo simulation study and applied to a cohort of patients undergoing traumatic orthopaedic surgery involving external fixators where a change in pin site infections is investigated. Results: The unconditional test controls the type I error rate at the nominal level and is uniformly more powerful than (or to be more precise uniformly at least as powerful as) Worsley's exact conditional test which is very conservative for small sample sizes. In the application a beneficial effect associated with the introduction of a new treatment procedure for pin site care could be revealed. Conclusions: We consider the new test an effective and easy to use exact test which is recommended in small sample size change point problems in binary sequences

    Validation of automatic passenger counting: introducing the t-test-induced equivalence test

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    Automatic passenger counting (APC) in public transport has been introduced in the 1970s and has been rapidly emerging in recent years. Still, real-world applications continue to face events that are difficult to classify. The induced imprecision needs to be handled as statistical noise and thus methods have been defined to ensure that measurement errors do not exceed certain bounds. Various recommendations for such an APC validation have been made to establish criteria that limit the bias and the variability of the measurement errors. In those works, the misinterpretation of non-significance in statistical hypothesis tests for the detection of differences (e.g. Student’s t-test) proves to be prevalent, although existing methods which were developed under the term equivalence testing in biostatistics (i.e. bioequivalence trials, Schuirmann in J Pharmacokinet Pharmacodyn 15(6):657–680, 1987) would be appropriate instead. This heavily affects the calibration and validation process of APC systems and has been the reason for unexpected results when the sample sizes were not suitably chosen: Large sample sizes were assumed to improve the assessment of systematic measurement errors of the devices from a user’s perspective as well as from a manufacturers perspective, but the regular t-test fails to achieve that. We introduce a variant of the t-test, the revised t-test, which addresses both type I and type II errors appropriately and allows a comprehensible transition from the long-established t-test in a widely used industrial recommendation. This test is appealing, but still it is susceptible to numerical instability. Finally, we analytically reformulate it as a numerically stable equivalence test, which is thus easier to use. Our results therefore allow to induce an equivalence test from a t-test and increase the comparability of both tests, especially for decision makers

    Analysis of high-dimensional one group repeated measures designs

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    We propose a novel one sample test for repeated measures designs and derive its limit distribution for the situation where both the sample size n as well as the dimension d of the observations go to infinity. This covers the high-dimensional case with d > n. The tests are based on a quadratic form which involve new unbiased and dimension-stable estimators of different traces of the underlying unrestricted covariance structure. It is shown that the asymptotic distribution of the statistic may be standard normal, standardized chi(2)-distributed, or even of weighted chi(2)-form in some situations. To this end, we suggest an approximation technique which is asymptotically valid in the first two cases and provides an accurate approximation for the latter. We motivate and illustrate the application with a sleep lab data set and also discuss the practical meaning of d -> infinity in case of repeated measures designs. It turns out that the limit behaviour depends on how the number of repeated measures is increased which is crucial for application.German Research Foundation [DFG-PA 2409/3-1

    In-vivo durability of a fluoride-releasing sealant (OpalSeal) for protection against white-spot lesion formation in orthodontic patients

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    Background Sealant application during fixed appliances orthodontic treatment for enamel protection is common, however, reliable data on its durability in vivo are rare. Objective This study aims at assessing the durability of a sealant (OpalSeal, Ultradent) for protection against white-spot lesion formation in orthodontic patients over 26 weeks in vivo, taking into account the provision or absence of an adequate oral hygiene. We tested the null hypothesis of (1) no significant abatement of the sealant after 26 weeks in fixed orthodontic treatment compared to baseline, and (2) no significant influence of the factor of brushing and oral hygiene (as screened by approximal plaque index, API) on the abatement of the sealant. Methods Integrity and abatement of OpalSeal applicated directly following bracketing was assessed in thirty-six consecutive patients (nteeth = 796) undergoing orthodontic treatment with fixed appliances (male/female12/24; mean age/SD 14.4/1.33 Y). Assessment of the fluorescing sealant preservation was by a black-light lamp, using a classification that was concepted in analogy to the ARI index: (3, sealant completely preserved; 2= > 50% preserved; 1 = 80%). Results At baseline, 43.4% of teeth had a positive API. Oral hygiene deteriorated after bracketing (T1, 53%) significantly. Null hypothesis (1) was rejected, while (2) was accepted: Mean values of both the well brushed and non-brushed anterior teeth undercut the score “1” at T3 (week 14). Despite a slightly better preservation of the sealer before and after T3 in not-sufficiently brushed (API-positive) teeth, this finding was statistically not significant. Conclusion One single application of OpalSeal is unlikely to last throughout the entire fixed appliance treatment stage. On average, re-application of the sealant can be expected to be necessary after 3.5 months (week 14) in treatment

    Exact change point detection with improved power in small‐sample binomial sequences

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    To detect a change in the probability of a sequence of independent binomial random variables, a variety of asymptotic and exact testing procedures have been proposed. Whenever the sample size or the event rate is small, asymptotic approximations of maximally selected test statistics have been shown to be inaccurate. Although exact methods control the type I error rate, they can be overly conservative due to the discreteness of the test statistics in these situations. We extend approaches by Worsley and Halpern to develop a test that is less discrete to increase the power. Building on ideas from binary segmentation, the proposed test utilizes unused information in the binomial sequences to add a new ordering to test statistics that are of equal value. The exact distributions are derived under side conditions that arise in hypothetical segmentation steps and do not depend on the type of test statistic used (e.g., log likelihood ratio, cumulative sum, or Fisher's exact test). Using the proposed exact segmentation procedure, we construct a change point test and prove that it controls the type‐I‐error rate at any given nominal level. Furthermore, we prove that the new test is uniformly at least as powerful as Worsley's exact test. In a Monte Carlo simulation study, the gain in power can be remarkable, especially in scenarios with small sample size. Giving a clinical database example about pin site infections and an example assessing publication bias in neuropsychiatric drug research, we demonstrate the wide‐ranging applicability of the test
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