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A Randomised Controlled Trial of ePROM-Guided Flexible Scheduling in Dermatology
Sponsor: National University Hospital, Singapore
Summary
The goal of this clinical trial is to evaluate whether an electronic patient-reported outcome measure (ePROM)-guided flexible scheduling system can improve outpatient clinic resource utilisation in patients attending dermatology outpatient clinics for routine follow-up. The main questions it aims to answer are: * Does the intervention reduce the number of actualised outpatient visits over 12 months compared with standard fixed scheduling? * Does the intervention group achieve higher adherence to monthly ePROM monitoring, as measured by the proportion of completed ePROM submissions?
Key Details
Gender
All
Age Range
16 Years - Any
Study Type
INTERVENTIONAL
Enrollment
250
Start Date
2026-09
Completion Date
2029-12
Last Updated
2026-03-18
Healthy Volunteers
No
Interventions
Flexible ePROM-guided Scheduling System
Monthly ePROM responses will feed a Bayesian decision system to determine appointment need, which will then be used to make recommendations to patients for scheduling of appointments.
electronic patient reported outcome measures (ePROMs)
Monthly electronic patient reported outcome measures (ePROMs) surveys will be sent to patients' mobile devices to capture self-reported disease severity data.