Use of a Digital Psychotherapeutic App to Reduce Symptom Burden in Dermatology Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age16+
SponsorNational University Hospital, Singapore

About this trial

Skin diseases, despite low mortality, significantly impair quality of life. This randomised controlled trial evaluates the efficacy of a digital toolkit comprising psychotherapeutic strategies in reducing QoL burden in patients with chronic inflammatory skin conditions. This toolkit is hosted on a mobile application and will be used by study participants randomised to the intervention arm over the 32 week study period.

Eligibility criteria

Qualifiers

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

Disqualifiers

Patients with active psychiatric symptoms (e.g. active suicidal ideation, psychosis, delusions)

Patients with unstable psychiatric condition, characterized by

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

Trial design

Treatments tested in this trial

  • Digital psychotherapeutic intervention
  • Healthy365

Treatment groups

690 Participants
are divided into 2 treatment groups

Sponsors and collaborators

National University Hospital, Singapore

Lead sponsor

National Skin Centre, Singapore

Collaborator

National University of Singapore

Collaborator

KK Women's and Children's Hospital

Collaborator