Atopic dermatitis
Conditions
Interventions
The ePRO system uses Integrity Healthcare'
s YaDoc. After obtaining consent for participation in this study from the research subject patient, install the application on the smartphone owned by the research subject according to the YaDoc opera
s photography function. The recording period shall be 8 weeks. Before the start and at the end of the study, a questionnaire survey will be conducted on the research subjects to examine the usefulness
Sponsors
Nagasaki University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1 Patients with atopic dermatitis who are 18 years of age or older at the time of informed consent 2 Patients judged by the investigator that patient data collection by ePRO is effective 3 Smartphone (iOS, Android) users
Exclusion criteria
Exclusion criteria: 1 Cases where it is difficult to see, operate, and understand YaDoc and smartphones 2 Patients participating in a clinical study with other interventions at the start of this study 3 Other patients who are judged by doctors to be unfavorable subjects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patients' satisfaction and challenges with using ePRO will be assessed using patient questionnaires at the beginning and after 8 weeks. | — |
Countries
Japan
Contacts
Public ContactMotoi Takenaka
Nagasaki University Hospital Dermatology and Allergology
Outcome results
None listed