2019
DOI: 10.3390/diagnostics9030067
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Establishing Clinical Utility for Diagnostic Tests Using a Randomized Controlled, Virtual Patient Trial Design

Abstract: Demonstrating clinical utility for diagnostic tests and securing coverage and reimbursement requires high quality and, ideally, randomized controlled trial (RCT) data. Traditional RCTs are often too costly, slow, and cumbersome for diagnostic firms. Alternative data options are needed. We evaluated four RCTs using virtual patients to demonstrate clinical utility. Each study used a similar pre-post intervention, two round design to facilitate comparison. Representative samples of physicians were recruited and r… Show more

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Cited by 5 publications
(6 citation statements)
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“…The limitations of this study include the use of simulated patients; however, other research comparing simulated patient research with real-world patient studies indicates that real-world studies would broadly substantiate this study's findings ( 38 , 39 ). We used a national sample of gastroenterologists and GI surgeons.…”
Section: Discussionmentioning
confidence: 73%
“…The limitations of this study include the use of simulated patients; however, other research comparing simulated patient research with real-world patient studies indicates that real-world studies would broadly substantiate this study's findings ( 38 , 39 ). We used a national sample of gastroenterologists and GI surgeons.…”
Section: Discussionmentioning
confidence: 73%
“…The newer approach uses validated patient simulations in randomized clinical trials, which are lower cost and less time-intensive than large, multicenter, patient-based trials. CPVs, which are extensively validated simulated patients, [10,11,17,18] have important advantages over real-world patients: (1) they specify the use case and eliminate patient heterogeneity;…”
Section: Discussionmentioning
confidence: 99%
“…The newer approach uses validated patient simulations in randomized clinical trials, which are lower cost and less time-intensive than large, multicenter, patient-based trials. CPVs, which are extensively validated simulated patients, [ 10 , 11 , 17 , 18 ] have important advantages over real-world patients: (1) they specify the use case and eliminate patient heterogeneity; (2) they focus on whether the test changes physician behavior; and (3) they can generate high-quality data in short periods of time. Despite CPVs’ ability to track actual clinical practice in multiple settings among a legion of clinical conditions, for some, the question remains as to how well these changes in CPVs translate into specific changes in clinical practice and better outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…They are also conceptually complex because new molecular tests provide information informing individual decisions that are dependent on human beliefs and behaviours [57], as well as the organisations infrastructure and resources to respond. Evidence may need to include real world data [58], virtual patient trial design [59] and proposals for more efficient trial methodologies that assess the realisable clinical benefit of CMg tests will be welcomed.…”
Section: A Route To Implementation In the Healthcare Systemmentioning
confidence: 99%