Realising the full potential of data-enabled trials in the UK: a call for action

Author:

Sydes Matthew RORCID,Barbachano Yolanda,Bowman LouiseORCID,Denwood TomORCID,Farmer AndrewORCID,Garfield-Birkbeck StephORCID,Gibson MartinORCID,Gulliford Martin CORCID,Harrison David AORCID,Hewitt CatherineORCID,Logue JenniferORCID,Navaie Will,Norrie JohnORCID,O'Kane Martin,Quint Jennifer KORCID,Rycroft-Malone JoORCID,Sheffield Jonathan,Smeeth LiamORCID,Sullivan FrankORCID,Tizzard Juliet,Walker Paula,Wilding JohnORCID,Williamson Paula RORCID,Landray MartinORCID,Morris AndrewORCID,Walker Rhoswyn RORCID,Williams Hywel CORCID,Valentine Janet

Abstract

RationaleClinical trials are the gold standard for testing interventions. COVID-19 has further raised their public profile and emphasised the need to deliver better, faster, more efficient trials for patient benefit. Considerable overlap exists between data required for trials and data already collected routinely in electronic healthcare records (EHRs). Opportunities exist to use these in innovative ways to decrease duplication of effort and speed trial recruitment, conduct and follow-up.ApproachThe National Institute of Health Research (NIHR), Health Data Research UK and Clinical Practice Research Datalink co-organised a national workshop to accelerate the agenda for ‘data-enabled clinical trials’. Showcasing successful examples and imagining future possibilities, the plenary talks, panel discussions, group discussions and case studies covered: design/feasibility; recruitment; conduct/follow-up; collecting benefits/harms; and analysis/interpretation.ReflectionSome notable studies have successfully accessed and used EHR to identify potential recruits, support randomised trials, deliver interventions and supplement/replace trial-specific follow-up. Some outcome measures are already reliably collected; others, like safety, need detailed work to meet regulatory reporting requirements. There is a clear need for system interoperability and a ‘route map’ to identify and access the necessary datasets. Researchers running regulatory-facing trials must carefully consider how data quality and integrity would be assessed. An experience-sharing forum could stimulate wider adoption of EHR-based methods in trial design and execution.DiscussionEHR offer opportunities to better plan clinical trials, assess patients and capture data more efficiently, reducing research waste and increasing focus on each trial’s specific challenges. The short-term emphasis should be on facilitating patient recruitment and for postmarketing authorisation trials where research-relevant outcome measures are readily collectable. Sharing of case studies is encouraged. The workshop directly informed NIHR’s funding call for ambitious data-enabled trials at scale. There is the opportunity for the UK to build upon existing data science capabilities to identify, recruit and monitor patients in trials at scale.

Funder

National Institute of Health Research

Health Data Research UK

Medical Research Council

Clinical Practice Research Datalink

Publisher

BMJ

Subject

General Medicine

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