top of page
Statistical Methods for Contemporary Clinical Trials
Search


CCTMB #005 What are we talking about when we talk about decentralised clinical trials (DCTs)?
By Annie Wright, NIHR BRC PhD Candidate based at Imperial Clinical Trials Unit (ICTU) Decentralisation is the concept of moving trial procedures, e.g. recruitment or consent, away from a central location and towards participants. Different ways of decentralising can occur across the lifecycle of a trial: Stage of the Trial Traditional Decentralised Recruitment Recruitment at the trial site, with participants speaking to study staff Online recruitment, remote screening Conse
Sep 284 min read


CCTMB #004 Rethinking Evidence in Critical Care Trials: Perspectives from the Critical Care Reviews Meeting
By Manel Benlloch Guajardo and Martin Orr, Clinical Trials Statisticians at Imperial Clinical Trials Unit (ICTU) In June, members of the ICTU team attended the Critical Care Reviews meeting in Belfast. This stunning conference mixed groundbreaking critical care trials and independent editorials with the chance to experience first-hand the feeling of being in the Titanic grand staircase. A true blend of the novel and the antique. The conference delivered plenty of results but
Aug 247 min read


CCTMB #003 Sizing a Clinical Trial: Can't Test? – Don't Test
By Victoria Cornelius, Professor in Medical Statistics and Clinical Trials The design stage of a clinical trial is my favourite part of being a medical statistician, as there is no single perfect design. Instead, it offers a chance to discover and explore differing options. One aspect that many trialists struggle with is how to size the trial. This is unsurprising, as while the basic sample size calculation is simple and quick to perform, there is a lot more to take into cons
Jul 205 min read


CCTMB #002 Your Placebo Will See You Now: Controlling for Placebo Effects in Complex Intervention Trials
By Dr David Hohenschurz-Schmidt, Postdoctoral Researcher in Pain Research and Trial Methods for Complex Interventions Blinding is a fundamental principle of high-quality randomised controlled trials. It involves withholding key information about treatment allocation from trial participants (and often investigators and outcome assessors). The aim is to balance expectations across study groups so that any observed treatment effects can be more confidently attributed to the inte
Jun 224 min read


CCTMB #001 Can Bayesian Methods Help Us Learn More from Studies Within a Trial (SWATs)?
By Suzie Cro, Associate Professor in Medical Statistics and Clinical Trials Randomised controlled trials (RCTs) are the gold standard for testing new medical treatments. But what about testing how we run trials? That’s where a Study Within A Trial (SWAT) comes in. A SWAT is a small study embedded inside a larger host trial to test ways of improving trial processes, such as recruitment or retention strategies. SWATs are increasingly popular. But there’s a challenge, they a
May 203 min read
bottom of page