E55.9
Conditions
Interventions
Group 1: 20 young women,
three UV-exposures:
day 1 (skin type I 80 J/m², skin type II 100 J/m²)
day 3 (skin tye I 120 J/m², skin type II 150 J/m²)
day 5 (sin type I 150 J/m², sin type II 187.5 J/m²)
b
Sponsors
Charité Campus Charité Mitte
Eligibility
Sex/Gender
Female
Age
20 Years to 30 Years
Inclusion criteria
Inclusion criteria: female, age 20-30, healthy, reliable
Exclusion criteria
Exclusion criteria: skin or psychiatric conditions, oral Vitamin D intake, recent vacations to sunny countries
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| measuring 25-hydroxyvitamin d and 1,25-dihydroxyvitamin d at day 1, 8, 36 and 50, UV-exposures at day 1, 3 and 5 | — |
Secondary
| Measure | Time frame |
|---|---|
| measuring mood parameters (using Beck Depression Inventory (BDI) and Profille of mood states (POMS) self-rating questionnaires) at day 1 and 8, UV-exposures at day 1, 3 and 5 | — |
Countries
Germany
Contacts
Public ContactMaria Biersack
Charité-Universitätsmedizin Berlin, Department of Rheumatology and Clinical ImmunologyTeam Insider
Outcome results
None listed