vitiligo vulgaris
Conditions
Interventions
Participants will receive camouflage makeup application and instruction from trained cosmetology specialists using a dedicated cover foundation. Based on this guidance, they will perform self-applicat
Sponsors
Tohoku University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Disease/site: Vitiligo affecting exposed areas (face, neck, and hands) Age: 15 years or older; for participants under 18 years of age, parental consent is required Sex: No restriction Patients who have provided written informed consent to participate in the study and who attended a dermatology vitiligo clinic seeking camouflage makeup
Exclusion criteria
Exclusion criteria: History of allergy to cosmetics or presence of allergic reactions Patients scheduled to undergo additional surgery Patients who are objectively judged to lack the capacity to provide informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The Dermatology Life Quality Index (DLQI) will be used to evaluate improvements in quality of life associated with camouflage makeup. Assessments will be conducted before the intervention and after two weeks of continued use at home. | — |
Countries
Japan
Contacts
Public ContactMoyuka Irimada
Tohoku university hospital Dermatology
Outcome results
None listed