Handbook of Statistical Methods for Randomized Controlled Trials

ISBN-13: 9781498714624 / Angielski / Twarda / 2021 / 620 str.

Kyungmann Kim; Frank Bretz; Ying Kuen Cheung

Opis

This handbook is intended to serve as a reference text on statistical methods for randomized controlled trials. It can be used as a textbook for a graduate course in statistical methods for randomized controlled trials as well as a reference for those involved in the design, monitoring and analysis of randomized controlled trials.

Recenzje

"This book is the product of a large and outstanding group of editors and collaborative authors who undertook a huge effort of summarizing, in one volume, a subject spanning a wide crosssection of topics related to clinical trials. ... Throughout, many topics are illustrated with examples of recently reported trials adding to the applicability of the corresponding theory. The emphasis on sample size estimation is a very nice touch and a strong feature of the book. In some cases, authors have included code in R and SAS to assist users."
-Daniel Zelterman, in Technometrics, July 2022

Spis treści

Part I. Introduction to Randomized, Controlled Trials. 1. Introduction. Part II. Analytic Methods for Randomized, Controlled Trials. 2. Dichotomous and ordinal: chi-square and Fisher's exact tests and binary regression models. 3. Continuous: t-test, Wilcoxon-test, and linear or non-linear regression models. 4. Time to event subject to censoring: logrank test, Kaplan-Meier estimation and Cox proportional hazards regression models. 5. Count: Poisson and negative binomial regression models. 6. Longitudinal: Linear and generalized linear mixed models, GEE. 7. Recurrent events. 8. Cross-over design. 9. Factorial design. 10. Cluster randomized design. 11. Randomization, stratification, and outcome-adaptive allocation. 12. Sample size estimation and power analysis: Dichotomous, ordinal, continuous and count. 13. Sample size estimation and power analysis: Time-to-event data subject to censoring. 14. Sample size estimation and power analysis: Longitudinal data. 15. Group sequential methods, triangular methods and stochastic curtailments. 16. Sample size re-estimation. 17. Adaptive designs. 18. Multiple testing. 19. Subgroup analysis. 20. Competing risks. 21. Joint models for longitudinal markers and clinical outcomes. 22. Sequential multiple assignment randomization trial (SMART) for dynamic treatment allocation. 23. Safety data analysis. 24. Non-inferiority trials. 25. Incorporating historical data into RCTs. 26. Validation of surrogate outcomes.