NCT07481019

A Randomised Controlled Trial of ePROM-Guided Flexible Scheduling in Dermatology

• Status: Not Yet Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 250 (estimated)
• Sponsor: National University Hospital, Singapore · Academic / Other
• Sex: All
• Age: 16 Years
• Healthy volunteers: Not accepted

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?

Conditions

• Chronic Dermatological Conditions
• Eczema
• Urticaria
• Psoriasis

Interventions

Type	Name	Description
BEHAVIORAL	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.
BEHAVIORAL	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.

Timeline

• Start date: 2026-09-01
• Primary completion: 2029-06-01
• Completion: 2029-12-01
• First posted: 2026-03-18
• Last updated: 2026-03-18