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1.
Biometrics ; 57(1): 178-81, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11252595

ABSTRACT

When clinical studies require enrolled patients to have abnormal assays, the natural tendency of repeat measurements to regress toward the mean can lead to a false assessment of effectiveness of therapy. We propose a method to more accurately estimate the true effect of therapy by adjusting for a component of improvement that can be attributed to regression effect. The model we use allows for a combination of additive and/or multiplicative effects of the therapy.


Subject(s)
Biometry , Clinical Trials as Topic/statistics & numerical data , Regression Analysis , Cholesterol/blood , Confidence Intervals , Humans , Hypercholesterolemia/blood , Hypercholesterolemia/drug therapy , Models, Statistical , Monte Carlo Method , Randomized Controlled Trials as Topic/statistics & numerical data , Treatment Outcome
2.
Psychol Rep ; 89(2): 267-73, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11783546

ABSTRACT

A robust approach for the analysis of experiments with ordered treatment levels is presented as an alternative to existing approaches such as the parametric Abelson-Tukey test for monotone alternatives and the nonparametric Terpstra-Jonckheere test. The method integrates the familiar Spearman rank-order correlation with bootstrap routines to provide magnitude of association measures, p values, and confidence intervals for magnitude of association measures. The advantages of this method relative to five alternative approaches are pointed out.


Subject(s)
Analysis of Variance , Psychology, Experimental/statistics & numerical data , Psychometrics , Confidence Intervals , Humans , Statistics, Nonparametric
3.
Psychol Rep ; 87(1): 3-20, 2000 Aug.
Article in English | MEDLINE | ID: mdl-11026384

ABSTRACT

The important assumption of independent errors should be evaluated routinely in the application of interrupted time-series regression models. The two most frequently recommended tests of this assumption [Mood's runs test and the Durbin-Watson (D-W) bounds test] have several weaknesses. The former has poor small sample Type I error performance and the latter has the bothersome property that results are often declared to be "inconclusive." The test proposed in this article is simple to compute (special software is not required), there is no inconclusive region, an exact p-value is provided, and it has good Type I error and power properties relative to competing procedures. It is shown that these desirable properties hold when design matrices of a specified form are used to model the response variable. A Monte Carlo evaluation of the method, including comparisons with other tests (viz., runs, D-W bounds, and D-W beta), and examples of application are provided.


Subject(s)
Personality Inventory/statistics & numerical data , Psychometrics , Humans , Monte Carlo Method , Regression Analysis , Reproducibility of Results
4.
Psychol Methods ; 5(1): 87-101, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10937324

ABSTRACT

A new method for the analysis of linear models that have autoregressive errors is proposed. The approach is not only relevant in the behavioral sciences for analyzing small-sample time-series intervention models, but it is also appropriate for a wide class of small-sample linear model problems in which there is interest in inferential statements regarding all regression parameters and autoregressive parameters in the model. The methodology includes a double application of bootstrap procedures. The 1st application is used to obtain bias-adjusted estimates of the autoregressive parameters. The 2nd application is used to estimate the standard errors of the parameter estimates. Theoretical and Monte Carlo results are presented to demonstrate asymptotic and small-sample properties of the method; examples that illustrate advantages of the new approach over established time-series methods are described.


Subject(s)
Linear Models , Psychometrics , Regression Analysis , Bias , Humans , Likelihood Functions , Monte Carlo Method
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