The Value of Pragmatic Trials to Clinicians
Clinicians are always striving to improve the quality and the precision of care that they provide to their patients. Oftentimes, they’re lacking the information needed to make an optimal decision for an individual patient because much of the information they have at hand was either derived from a very broad and diverse population, or the population studied was demographically different than the population they are managing.
The evidence generated by randomized controlled trials (RCTs) may establish the potential efficacy, or clinical impact, of a drug, but it does not necessarily tell us how safe and effective it is for any given individual, or in whom it works best.
This issue, coupled with rapidly escalating costs in care delivery, makes it ever-more critical to generate high-quality, real-world evidence of value in an efficient manner.
Pragmatic clinical trials provide the optimal environment to address a broad spectrum of real-world issues, and generate evidence synergistic and complementary to RCTs. For clinicians, pragmatic trials generate evidence that enables better-informed decision making.
Pragmatic trials are studies designed for the primary purpose of informing decision-makers regarding the comparative balance of benefits, burdens and risks of a pharmaceutical, biomedical, surgical, or care management intervention at the patient level (Califf and Sugarman).
Clinicians can use pragmatic trials with several levels of engagement. They can become participating investigators, choose to enroll their patients in trials, or simply incorporate the learnings from the trials, through scientific publication, into their clinical practice.
HealthCore is among the early innovators and key promulgators of pragmatic trials on a national basis. We have conducted multiple studies within our research environment.