Bayesian decision-theoretic method and semi-parametric approach with applications in clinical trial designs and longitudinal studies

dc.contributor.advisorLee, J. Jacken_US
dc.contributor.committeeMemberCox, Dennis D.en_US
dc.contributor.committeeMemberScott, David W.en_US
dc.contributor.committeeMemberMa, Yanyuanen_US
dc.contributor.committeeMemberTapia, Richard A.en_US
dc.creatorJiang, Feien_US
dc.date.accessioned2014-09-16T15:12:12Zen_US
dc.date.available2014-12-01T06:10:03Zen_US
dc.date.created2013-12en_US
dc.date.issued2013-11-25en_US
dc.date.submittedDecember 2013en_US
dc.date.updated2014-09-16T15:12:12Zen_US
dc.description.abstractThe gold of biostatistical researches is to develop statistical tools that improves human health or increases understanding of human biology. One area of the studies focuses on designing clinical trials to find out if new drugs or treatments are efficacious. The other area focuses on studying diseases related variables, which gives better understanding of the diseases. The thesis explores these areas from both theoretical and practical points of views. In addition, the thesis develop statistical devices which improve the existing methods in these areas. Firstly, the thesis proposes a Bayesian decision-theoretic group sequential – adaptive randomization phase II clinical trial design. The design improves the trial efficiency by increasing statistical power and reducing required sample sizes. The design also increases patients’ individual benefit, because it enhances patients’ opportunities of receiving better treatments. Secondly, the thesis develops a semiparametric restricted moment model and a score imputation estimation for survival analysis. The method is more robust than the parametric alternatives. In addition to data analysis, the method is used to design a seamless phase II/III clinical trial. The seamless phase II/III clinical trial design shortens the durations between phase II and III studies, and improves the efficiency of the traditional designs by utilizing additional short term information for making decisions. Finally, the thesis develops a partial linear time varying semi-parametric single-index risk score model and a fused B-spline/kernel estimation for longitudinal data analysis. The method models confounder effects linearly. In addition, it uses a nonparametric nonlinear function, namely the single-index risk score, to model the effects of interests. The fused B-spline/kernel technique estimates both the parametric and nonparametric components consistently. The methodology is applied to study the onsite of Huntington’s disease in determining certain time varying covariate effects on the disease risk.en_US
dc.embargo.terms2014-12-01en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationJiang, Fei. "Bayesian decision-theoretic method and semi-parametric approach with applications in clinical trial designs and longitudinal studies." (2013) Diss., Rice University. <a href="https://hdl.handle.net/1911/77182">https://hdl.handle.net/1911/77182</a>.en_US
dc.identifier.urihttps://hdl.handle.net/1911/77182en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.subjectAdaptive randomizationen_US
dc.subjectB-splineen_US
dc.subjectBayesian decision-theoreticen_US
dc.subjectBiostatisticsen_US
dc.subjectClinical trialen_US
dc.subjectSemiparametric model and estimationen_US
dc.subjectKernel regressionen_US
dc.subjectSingle-index modelen_US
dc.titleBayesian decision-theoretic method and semi-parametric approach with applications in clinical trial designs and longitudinal studiesen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentStatisticsen_US
thesis.degree.disciplineEngineeringen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophyen_US
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