Abstract Background For certain conditions, treatments aim to lessen deterioration over time. A trial outcome could be change in a continuous measure, analysed using a random slopes model with a different slope in each treatment group. A sample size for a trial with a particular schedule of visits (e.g. annually for three years) can be obtained using a two-stage process. First, relevant (co-) variances are estimated from a pre-existing dataset e.g. an observational study conducted in a similar setting. Second, standard formulae are used to calculate sample size. However, the random slopes model assumes linear trajectories with any difference in group means increasing proportionally to follow-up time. The impact of these assumptions failing ...
Background: Platform trials can evaluate the efficacy of several experimental treatments compared to...
At the design phase of a clinical trial the total number of participants needed to detect a clinical...
Background: Design, conduct, and analysis of randomized clinical trials (RCTs) with time to event en...
Background: Most clinical trials with time-To-event primary outcomes are designed assuming constant ...
Trials of interventions that aim to slow disease progression may analyze a continuous outcome by co...
International audienceWe aimed to examine the extent to which inaccurate assumptions for nuisance pa...
We aimed to examine the extent to which inaccurate assumptions for nuisance parameters used to calcu...
We aimed to examine the extent to which inaccurate assumptions for nuisance parameters used to calcu...
Abstract Background Non-proportional hazards are common with time-to-event data but the majority of ...
<div><p>We aimed to examine the extent to which inaccurate assumptions for nuisance parameters used ...
It is well known that the statistical power of randomized controlled trials with a continuous outcom...
Background: External pilot or feasibility studies can be used to estimate key unknown parameters to ...
We discuss different methods of sample size calculation for two independent means, aiming to provide...
Item does not contain fulltextThe sample size required for a cluster randomised trial is inflated co...
We have previously derived power calculation formulas for cohort studies and clinical trials using t...
Background: Platform trials can evaluate the efficacy of several experimental treatments compared to...
At the design phase of a clinical trial the total number of participants needed to detect a clinical...
Background: Design, conduct, and analysis of randomized clinical trials (RCTs) with time to event en...
Background: Most clinical trials with time-To-event primary outcomes are designed assuming constant ...
Trials of interventions that aim to slow disease progression may analyze a continuous outcome by co...
International audienceWe aimed to examine the extent to which inaccurate assumptions for nuisance pa...
We aimed to examine the extent to which inaccurate assumptions for nuisance parameters used to calcu...
We aimed to examine the extent to which inaccurate assumptions for nuisance parameters used to calcu...
Abstract Background Non-proportional hazards are common with time-to-event data but the majority of ...
<div><p>We aimed to examine the extent to which inaccurate assumptions for nuisance parameters used ...
It is well known that the statistical power of randomized controlled trials with a continuous outcom...
Background: External pilot or feasibility studies can be used to estimate key unknown parameters to ...
We discuss different methods of sample size calculation for two independent means, aiming to provide...
Item does not contain fulltextThe sample size required for a cluster randomised trial is inflated co...
We have previously derived power calculation formulas for cohort studies and clinical trials using t...
Background: Platform trials can evaluate the efficacy of several experimental treatments compared to...
At the design phase of a clinical trial the total number of participants needed to detect a clinical...
Background: Design, conduct, and analysis of randomized clinical trials (RCTs) with time to event en...