About the design category
"Voracious demand for data" of pure probabilistic reasoning
Cumulative toxicity endpoint opinion
How to use p-values when sample sizes are not fixed
Cluster-Randomized Trial: Design Question
Precision as the goal for sample size estimation
Assigning time zero in an observational comparative effectiveness study
Can this be a possible statistical solution for a mid-trial realization?
Protocol deviation and its impact on stat analysis
Propensity score methods vs Penalized regression
Power and Sample Size Calculations in Pilot Studies
Health care experiences that altered your perspective on biostatistical ethics?
The role of simulation in developing analysis plans
How might we use Bayesian priors in observational studies of drug safety?
What is an adequate `pilot` study leading to a stepped-wedge cluster randomized trial
Estimating recruitment rate based on feasibility studies
Stratification, block-randomization, etc
next page →