Enhancing Cohorts

We're working to accelerate health data research by making it easier, faster, and more secure to link data from clinical cohorts with routine health records. This approach will help researchers uncover new insights into disease causes, progression, and treatment, improving patient care and outcomes.

Theme lead: Professor Reecha Sofat

Linking data from large, ‘omics-rich’ clinical cohorts with routine health records could transform our understanding of disease causes, progression, and treatment. Cohort studies provide powerful insights into cardiovascular and metabolic diseases, but their impact is often limited by the complexity, cost, and time required to link them with other health data.   

What we do

We coordinate the linkage of cardiovascular and diabetes cohort data with routine health records, reducing administrative and cost barriers while ensuring data security. Our work to develop a trusted research environment for clinical cohorts, UK CliC, enables researchers to:  

  • Access linked health data more quickly by streamlining applications and governance  
  • Reduce research costs by sharing data linkage expenses across studies  
  • Ensure data security through a trusted research environment  

Key areas of work

Hosting UK CliC: The UK Clinical Cohorts Trusted Research Environment

Expanding research potential through multimodal data

We will enhance cohort data by linking it with additional sources such as imaging, genomic, and biochemical data. This enables researchers to uncover deeper insights into disease mechanisms and treatment responses. 

Ensuring patient and public involvement (PPIE)

Public trust is at the heart of our work. Our UK CliC Patient and Public Involvement and Engagement Group ensures that patient perspectives shape how data is used. 

  • Co-produced FAQs to address public concerns.
  • Ongoing engagement to guide priorities for cohort research. 
  • Representation in oversight panels to ensure transparency and trust. 

What do we mean by ‘Enhancing Cohorts’? 

A cohort is a group of individuals participating in a research study, often sharing a common characteristic (e.g., people over 50 with atrial fibrillation). Researchers collect data such as blood tests, imaging, and genetic information. By enhancing cohorts, linking this data with routine health records (e.g., GP visits, hospital stays, prescriptions), we create a more complete picture of disease progression and treatment effectiveness.  

This approach helps researchers deliver faster, more impactful insights that lead to better patient outcome.