Clinical trial Recruiting at 1 site Interventional Ages 16 and up

Digital psychotherapeutic app to help people with eczema, psoriasis, or urticaria feel better

Official title: Development and Testing of a Digital Psychological Tool to Improve Symptom Burden in Dermatology Patients

Run by National University Hospital, Singapore · NCT06702293 · Data updated 2026-11-12

A mobile app delivering psychotherapeutic techniques is tested to see if it improves quality of life for people with inflammatory skin conditions.

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Quick facts

Study typeInterventional
Ages16 Years and up
SexAll
Enrollment690 (estimated)
SponsorNational University Hospital, Singapore
Academic / other
Locations1 site (Singapore)
StatusRecruiting
StartedFebruary 23, 2026
Main results expectedDecember 2028
Study endsJuly 2029
Registry record updatedSeptember 28, 2026
Trial IDNCT06702293 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are 16 years or older with psoriasis, eczema, or chronic urticaria, and a peak itch score of 4 or higher, who can use an English-language mobile app.

Probably not a fit

Patients without access to or comfort with mobile apps, or those with active psychiatric symptoms requiring immediate care, may derive limited or no benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial tests a mobile digital toolkit offering psychotherapeutic strategies such as mindfulness, CBT, and ACT for patients with eczema, psoriasis, or chronic urticaria. Participants are assigned to use the app over a 32-week period to see if it reduces QoL burden compared with standard care. The study focuses on whether integrating mental health approaches within dermatology care can improve patient-reported outcomes and daily functioning. The app targets skin-related itch, sleep disturbance, anxiety, and depression associated with chronic inflammatory skin diseases. The trial also evaluates how the intervention can be implemented within real-world dermatology settings.

Why it matters

Potential benefit: If successful, participants may experience reduced itch-related distress and improved quality of life through accessible, app-based mental health support.

How similar studies have gone: Prior pharmacologic and psychotherapeutic approaches have shown benefits in mental health and dermatology, but evidence for dermatology-specific digital psychotherapies remains limited and this trial adds new, practical data.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients with psoriasis, eczema or chronic urticaria diagnosed by a dermatologist
* Aged 16 or older
* Peak pruritus intensity of 4 or more on a 11-point numerical rating scale (0-10, with 10 representing worst itch)
* Able to engage with a mobile application in the English language

Exclusion Criteria:

* Patients with active psychiatric symptoms (e.g. active suicidal ideation, psychosis, delusions)
* Patients with unstable psychiatric condition, characterized by

  o Hospital inpatient admission for a psychiatric condition or initiation of a psychotropic medication in the prior 3 months
* Patients with unstable dermatological condition, characterized by

  * Recent flare of the skin condition within the last 2 weeks, including diagnosis of a flare by a doctor, use of systemic steroids, oral antibiotics, wet wrap rescue therapy, oral antivirals, or increase in frequency of phototherapy or dose of systemic medications for the dermatological condition within the last 2 weeks OR
  * Any of the following within 3 months

    * inpatient admission for a dermatological condition
    * Initiation of phototherapy
    * Initiation of systemic therapy (conventional immunosuppressive agent, biologics, JAK inhibitors) within the last 3 months.

Where it's running

  • National University Hospital
    Singapore, Singapore
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.