About this trial
The primary objective is to determine if the use of the colonoscopy surveillance recommendations algorithm increases the accuracy of surveillance timing recommendations compared to traditional methods. The secondary objective is to assess the time required to make surveillance recommendations with and without the algorithm, determine the efficiency gains (the average time saved per recommendation), and evaluate the opportunity cost (the financial value of the time saved).
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Gastroenterologists and primary care physicians, including residents and fellows, currently practicing at NYU Langone Health, and Bellevue.
Willing and able to provide consent
Disqualifiers
Physicians not practicing in relevant fields or those with conflicts of interest.
Trial population
Gastroenterologists and primary care physicians.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Accuracy of surveillance timing recommendations
Time taken to answer each scenario
Sponsors and contacts
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