Supporting clinical trials or other research studies
From design and analysis to interpretation and reporting of all types of study
We have extensive experience in providing statistical support to clinical trials including feasibility (for example, the
EMaPP feasibility trial
and ) and pilot trials, randomised controlled trials including CTIMPs (for example ), adaptive designs, cluster trials (for example, ), stepped-wedge trials, early phase trials (for example, ), trials of complex interventions, and other well designed research studies including observational longitudinal studies such as
SWIMS
and the
EarlyBird
study. We work across the whole life cycle of trials and can offer support and advice in the following areas:
- study design – including sample size and power calculations
- grant and protocol writing – advice on the data that you plan to collect and how these data will result in meaningful conclusions
- advice on writing Statistical Analysis Plans (SAPs)
- data management – eCRF