There are several methodological challenges when conducting randomised controlled trials in palliative care. These include worsening function and high mortality, leading to treatment discontinuation, some of which will be unrelated to the intervention being evaluated.Recently, a new framework for handling postrandomisation events, such as attrition, has been released. This framework aims to align trial objectives, design, conduct and analysis by clarifying what and how to estimate treatment effects in the presence of data affected by postrandomisation events.The purpose of this paper is to introduce palliative care researchers to this framework and how it can guide trial design, and efficacy and safety analysis in a palliative care context ...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...
There are several methodological challenges when conducting randomised controlled trials in palliati...
There are several methodological challenges when conducting randomised controlled trials in palliati...
There are several methodological challenges when conducting randomised controlled trials in palliati...
CONTEXT: Missing data are common in hospice/palliative care randomized trials due to high drop-out b...
Background:Statistical analysis in palliative and end-of-life care research can be problematic due t...
Background: Statistical analysis in palliative and end-of-life care research can be problematic due ...
Background:Statistical analysis in palliative and end-of-life care research can be problematic due t...
Background:Statistical analysis in palliative and end-of-life care research can be problematic due t...
Background:: Missing data can introduce bias and reduce the power, precision and generalisability of...
© 2016 The Authors. Published by Elsevier Inc. Objectives To assess the risk posed by missing data (...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...
There are several methodological challenges when conducting randomised controlled trials in palliati...
There are several methodological challenges when conducting randomised controlled trials in palliati...
There are several methodological challenges when conducting randomised controlled trials in palliati...
CONTEXT: Missing data are common in hospice/palliative care randomized trials due to high drop-out b...
Background:Statistical analysis in palliative and end-of-life care research can be problematic due t...
Background: Statistical analysis in palliative and end-of-life care research can be problematic due ...
Background:Statistical analysis in palliative and end-of-life care research can be problematic due t...
Background:Statistical analysis in palliative and end-of-life care research can be problematic due t...
Background:: Missing data can introduce bias and reduce the power, precision and generalisability of...
© 2016 The Authors. Published by Elsevier Inc. Objectives To assess the risk posed by missing data (...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...
Background: Missing data compromise the internal and external validity of trial findings, however th...