Professor of Medical Statistics at The University of Sheffield and NIHR Senior Investigator. Statistician, walker and Garibaldi Red. The opinions are personal
If anyone can help with this survey or school age children it would be appreciated
Please share and/or post to any persons or groups that may be interested....
Had a paper published with @Flight_LG and @Alan_Brennan entitled
Value-adaptive clinical trial designs for efficient delivery of publicly funded trials - a discussion of methods, case studies, opportunities and challenges
https://t.co/ClAICWzYBC
The protocol for MissionEB - a randomised, double-blinded, placebo-controlled, two-centre, crossover trial - a study to assess mesenchymal intravenous stromal cell infusions in children with recessive dystrophic epidermolysis bullosa has been published
https://t.co/sXQ162pPLP
Attending an excellent talk by @NikkiTotton entitled at #SCT2025 entitled
Using benefit risk methods to adjust the non-inferiority margin based on treatment benefits
We recommend that the conditional frailty model be used for these data in trials, including cluster randomised trials, to help
to explain changes in event risk over time and assist clinical interpretation
In clinical trials it is not only potential benefits that should be measured - it is crucially important that any potential #harms are also investigated 1/7
#MethodologyMonday #118
New Publication 🔊: Trials special series - the collection, analysis and reporting of adverse events in randomised controlled trials by @RachPips & @VR_Cornelius https://t.co/gfD8cDV9yK
My PhD student is undertaking a DELPHI on reporting of sample sizes with studies with adaptive designs in protocols and grants. Please fill in if you can
New Paper! Routinely recorded primary care data can be used to evaluate interventions provided within routine care, anecdotally researchers in the @AUKCAR have encountered multiple barriers to access and use.
https://t.co/wBTNXlZxBK
My paper with Amy Whitehead Mike Campbell & Cindy Cooper
Estimating the sample size for a pilot randomised trial to minimise the overall trial sample size for the external pilot and main trial for a continuous outcome variable
Has been cited 1000 times
https://t.co/VyBZQP6zAC
Just had a paper published entitled "A review of UK publicly funded non-inferiority trials: is the design more inferior than it should be?"
Led by Nikki Totton with Stephen Walters and Elizabeth Coates
https://t.co/g2ejmilMXB
The timing of the first inteim analysis between industry and publicly funded trials is quite marked. For industry studies the first interim is after 50% of the information fration. By comparison for publicly funded trials the timing is bi-modal
Justed had paper published with @qiangzh83769692 , @mdimairo , Jen Lewis and Zihang Yu entitled
"Reporting and communication of sample size calculations in adaptive clinical trials: a review of trial protocols and grant applications"
https://t.co/oXpiJ9PSv5