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

Starting soon · Not applicable

Conditions studied: Chronic Dermatological Conditions, Eczema, Urticaria, Psoriasis, Acne

In brief

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 facts

Study ID

NCT07481019

Run by

National University Hospital, Singapore

People needed

250

Starts

2026-09-01

Expected to finish

2029-12-01

Last updated by the study team

2026-07-01

Who can join

Age: 16 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Dermatology outpatients otherwise due for a follow-up appointment within six months.
• Ability to independently navigate and complete ePROMs.
• Ability to provide informed consent (including parental consent for minors).

You may not qualify if…

• Patients who require fixed or scheduled in-person visits, including those needing skin cancer surveillance, bedside procedures (e.g., liquid nitrogen therapy), surgical interventions, or routine blood tests for immunosuppressive therapy.

Full record on ClinicalTrials.gov

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