Data Enabled Clinical Trials

By integrating routinely collected NHS health data into clinical trials, we’re helping researchers recruit participants more effectively, reduce administrative burdens, and generate real-world evidence that can lead to quicker, more impactful advances in cardiovascular care.

Former theme lead: Professor Matt Sydes

Clinical trials are the gold standard for testing new treatments, but they can be expensive, slow, and resource-intensive. Right now, most UK trials don’t fully tap into the wealth of NHS data that already exists. 

If you’re looking to integrate routinely collected NHS health data into your trial, we’d love to help. Get in touch.

What we do 

We work closely with triallists, clinicians, and data scientists to create the tools, resources, and infrastructure needed to enable and enhance data-enabled clinical trials. 

By using real-world healthcare data, we can: 

  • Identify and invite trial participants faster 
  • Ensure diverse and representative trial populations 
  • Reduce duplication of data collection and entry 
  • Minimise costly trial monitor site visits and admin work 
  • Improve long-term participant follow-up 

This means more trials, better data, and faster benefits for patients. 

Key areas of work

Helping researchers navigate health data for trials

We provide practical guidance on how to access, use, and interpret NHS health data in cardiovascular trials.
Data resources for clinical trials
Report: How to facilitate the use of healthcare systems data in trials

We’re also developing a Data Utility Comparison (DUCk) study – a Study Within A Trial (SWAT) – to assess how well routinely collected NHS data performs compared to traditional trial data collection.

In collaboration with HDR UK, the Transforming Data for Trials programme is also working to transform access to, and the utility, analysis and understanding of healthcare systems data to enable its use in clinical trials – providing research teams with the same reliable outcomes with less effort and reduced costs.

Developing consistent and clinically agreed data-based outcomes for trials

Consistent and clinically agreed phenotypes and outcomes are critical when planning, running, and interpreting findings from clinical trials.

The SCORE-CVD (Standardising Clinical Outcome measures in Routinely collected Electronic healthcare systems data) project brings together clinical experts, triallists, and health data scientists, and public contributors to standardise trial outcome measures by defining consistent, high-quality trial outcome measures using NHS health data.

Priority outcomes include:

  • Heart attack (Myocardial Infarction)
  • Stroke
  • Cardiovascular death
  • Heart failure
  • Major bleeding

We’ll continue to share progress and updates from this work, with findings from this project having the potential to support the clinical trial community with new resources to finetune future trials.

Read the SCORE-CVD initial report

 

Areas of work

Find out more about our data-led research.