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Design and Analysis of Quality of Life Studies in Clinical Trials - Diane L. Fairclough

Design and Analysis of Quality of Life Studies in Clinical Trials

Buch | Hardcover
424 Seiten
2010 | 2nd edition
Chapman & Hall/CRC (Verlag)
978-1-4200-6117-8 (ISBN)
CHF 235,65 inkl. MwSt
Presents a range of solutions to analytic issues. This title reflects developments in methodology with coverage of mixture models and a dataset example. It implements examples using SAS and R code and incorporates a number of examples from real QoL clinical trials to illustrate design and analysis methods.
Design Principles and Analysis Techniques for HRQoL Clinical Trials
SAS, R, and SPSS examples realistically show how to implement methods

Focusing on longitudinal studies, Design and Analysis of Quality of Life Studies in Clinical Trials, Second Edition addresses design and analysis aspects in enough detail so that readers can apply statistical methods, such as mixed effect models, to their own studies. The author illustrates the implementation of the methods using the statistical software packages SAS, SPSS, and R.

New to the Second Edition






Data sets available for download online, allowing readers to replicate the analyses presented in the text
New chapter on testing models that involve moderation and mediation
Revised discussions of multiple comparisons procedures that focus on the integration of health-related quality of life (HRQoL) outcomes with other study outcomes using gatekeeper strategies
Recent methodological developments for the analysis of trials with missing data
New chapter on quality adjusted life-years (QALYs) and QTWiST specific to clinical trials
Additional examples of the implementation of basic models and other selected applications in R and SPSS

This edition continues to provide practical information for researchers directly involved in the design and analysis of HRQoL studies as well as for those who evaluate the design and interpret the results of HRQoL research. By following the examples in the book, readers will be able to apply the steps to their own trials.

Diane L. Fairclough is a professor in the Department of Biostatistics and Informatics in the Colorado School of Public Health and director of the Biostatistics Core of the Colorado Health Outcomes Program at the University of Colorado in Denver. She is also President of the International Society for Quality of Life Research. Dr. Fairclough’s prior appointments include St. Jude Children’s Research Hospital, Harvard School of Public Health, and AMC Cancer Research Center.

Introduction and Examples. Study Design and Protocol Development. Models for Longitudinal Studies I. Models for Longitudinal Studies II. Moderation and Mediation. Characterization of Missing Data. Analysis of Studies with Missing Data. Simple Imputation. Multiple Imputation. Pattern Mixture and Other Mixture Models. Random Effects Dependent Dropout. Selection Models. Multiple Endpoints. Composite Endpoints and Summary Measures. Quality Adjusted Life-Years (QALYs) and Q-TWiST. Analysis Plans and Reporting Results. Appendices. References.

Erscheint lt. Verlag 12.1.2010
Reihe/Serie Chapman & Hall/CRC Interdisciplinary Statistics
Zusatzinfo 87 Tables, black and white; 69 Illustrations, black and white
Sprache englisch
Maße 156 x 234 mm
Gewicht 748 g
Themenwelt Medizin / Pharmazie
ISBN-10 1-4200-6117-8 / 1420061178
ISBN-13 978-1-4200-6117-8 / 9781420061178
Zustand Neuware
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