We propose a Bayesian decision theoretic model of a fully sequential experiment in which the real‐valued primary end point is observed with delay. The goal is to identify the sequential experiment which maximizes the expected benefits of technology adoption decisions, minus sampling costs. The solution yields a unified policy defining the optimal ‘do not experiment’–‘fixed sample size experiment’–‘sequential experiment’ regions and optimal stopping boundaries for sequential sampling, as a function of the prior mean benefit and the size of the delay. We apply the model to the field of medical statistics, using data from published clinical trials
We investigate value-based clinical trial design by applying a Bayesian decisiontheoretic model of a...
The design of sequential experiments and, in particular, randomised controlled trials involves a tra...
In the conduct of sequential clinical trials, primary statistical issues include design, monitoring ...
We propose a Bayesian decision theoretic model of a fully sequential experiment in which the real‐va...
We propose a Bayesian decision-theoretic model of a fully sequential experiment in which the real-va...
We present a Bayesian sequential sampling model in which a researcher has flexibility over the timin...
In this paper we consider a method for monitoring a clinical trial whose patients are sequentially e...
We study the optimal investment/abandonment decision for a project, where costly sequential experime...
In sequential experiments the sample size is not planned in advance. Data are progressively collecte...
We propose a class of phase II clinical trial designs with sequential stopping and adaptive treatmen...
Background/Aims: There is growing interest in the use of adaptive designs to improve the efficiency ...
When conducting a randomized comparative clinical trial, ethical, scientific or economic considerati...
[[abstract]]In the sequential analysis of data, both Bayesian and frequentist methods often make use...
Unlike traditional approaches Bayesian methods enable formal combination of expert opinion and obje...
this paper, we offer a fully Bayesian approach to this problem, specifying not only the likelihood a...
We investigate value-based clinical trial design by applying a Bayesian decisiontheoretic model of a...
The design of sequential experiments and, in particular, randomised controlled trials involves a tra...
In the conduct of sequential clinical trials, primary statistical issues include design, monitoring ...
We propose a Bayesian decision theoretic model of a fully sequential experiment in which the real‐va...
We propose a Bayesian decision-theoretic model of a fully sequential experiment in which the real-va...
We present a Bayesian sequential sampling model in which a researcher has flexibility over the timin...
In this paper we consider a method for monitoring a clinical trial whose patients are sequentially e...
We study the optimal investment/abandonment decision for a project, where costly sequential experime...
In sequential experiments the sample size is not planned in advance. Data are progressively collecte...
We propose a class of phase II clinical trial designs with sequential stopping and adaptive treatmen...
Background/Aims: There is growing interest in the use of adaptive designs to improve the efficiency ...
When conducting a randomized comparative clinical trial, ethical, scientific or economic considerati...
[[abstract]]In the sequential analysis of data, both Bayesian and frequentist methods often make use...
Unlike traditional approaches Bayesian methods enable formal combination of expert opinion and obje...
this paper, we offer a fully Bayesian approach to this problem, specifying not only the likelihood a...
We investigate value-based clinical trial design by applying a Bayesian decisiontheoretic model of a...
The design of sequential experiments and, in particular, randomised controlled trials involves a tra...
In the conduct of sequential clinical trials, primary statistical issues include design, monitoring ...