When performing a repeated measures experiment, such as a clinical trial, there is a risk of subject drop-out during the experiment. If one or more subjects leave the study prematurely, a situation could arise where the eventual design is disconnected, implying that very few treatment contrasts for both direct effects and carryover effects are estimable. This paper aims to identify experimental conditions where this problem with the eventual design can be avoided. It is shown that in the class of uniformly balanced repeated measurement designs consisting of two or more Latin squares, there are planned designs with the following useful property. Provided that all subjects have completed the first two periods of study, such a design will not ...
Multiarm trials with follow-up on participants are commonly implemented to assess treatment effects ...
We discuss inference for longitudinal clinical trials subject to possibly informative dropout. A sel...
We discuss inference for longitudinal clinical trials subject to possibly informative dropout. A sel...
When performing a repeated measures experiment, such as a clinical trial, there is a risk of subject...
In scientific experiments where human behaviour or animal response is intrinsically involved, such a...
Abstract: Low, Lewis and Prescott (1999) showed that a crossover design based on a Williams Latin sq...
A cross-over study is a comparitive experiment in which subjects receive a sequence of two or more t...
PhDIn a trial with a crossover design, participants receive a sequence of treatments over two or m...
Multiarm trials with follow‐up on participants are commonly implemented to assess treatment effects ...
In some crossover experiments, particularly in medical applications, subjects may fail to complete t...
Multiarm trials with follow-up on participants are commonly implemented to assess treatment effects ...
The assumption of carryover effects is unavoidable due to the very nature of crossover designs. Even...
A crossover study is a repeated measures design in which each subject is randomly assigned to a sequ...
The reduced efficiency of the cluster randomized trial design may be compensated by implementing a m...
Multiarm trials with follow-up on participants are commonly implemented to assess treatment effects ...
We discuss inference for longitudinal clinical trials subject to possibly informative dropout. A sel...
We discuss inference for longitudinal clinical trials subject to possibly informative dropout. A sel...
When performing a repeated measures experiment, such as a clinical trial, there is a risk of subject...
In scientific experiments where human behaviour or animal response is intrinsically involved, such a...
Abstract: Low, Lewis and Prescott (1999) showed that a crossover design based on a Williams Latin sq...
A cross-over study is a comparitive experiment in which subjects receive a sequence of two or more t...
PhDIn a trial with a crossover design, participants receive a sequence of treatments over two or m...
Multiarm trials with follow‐up on participants are commonly implemented to assess treatment effects ...
In some crossover experiments, particularly in medical applications, subjects may fail to complete t...
Multiarm trials with follow-up on participants are commonly implemented to assess treatment effects ...
The assumption of carryover effects is unavoidable due to the very nature of crossover designs. Even...
A crossover study is a repeated measures design in which each subject is randomly assigned to a sequ...
The reduced efficiency of the cluster randomized trial design may be compensated by implementing a m...
Multiarm trials with follow-up on participants are commonly implemented to assess treatment effects ...
We discuss inference for longitudinal clinical trials subject to possibly informative dropout. A sel...
We discuss inference for longitudinal clinical trials subject to possibly informative dropout. A sel...