Skin Barrier Function Comparison in Women Using and Not Using UV Nail Lamps
This observational study aims to compare the skin barrier function in women who use UV nail lamps and those who do not, by measuring changes in transepidermal water loss, skin hydration, and skin erythema.
Data Collection
Collected at a single point in time - Cross-sectionalSigns and Symptoms+3
+ Skin Diseases
+ Skin Manifestations
Case-Control
Comparing exposures between individuals with and without disease in order to identify potential risk factors.Summary
Study start date: July 1, 2026
Actual date on which the first participant was enrolled.This study focuses on comparing the skin's protective barrier in healthy adult women who regularly use UV lamps for nail treatments and those who do not. The main aim is to understand if regular use of UV lamps impacts the skin's barrier function. The study also explores if the duration of UV lamp use influences the skin's protective abilities. This research holds significance as it can provide insights into the potential effects of UV lamps on skin health, addressing a common yet often overlooked aspect of beauty routines. Participants in this study will attend a single visit where they will complete a brief questionnaire about their nail care habits and the duration of UV lamp use. They will then undergo non-invasive tests to measure the skin's barrier function on their hands. These tests include assessing transepidermal water loss, which indicates how well the skin retains moisture, skin hydration levels, and skin redness or erythema. These measurements will help researchers understand the potential impact of UV lamps on various aspects of skin health.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.30 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-Control
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 18 to 50 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
University of Split School of Medicine
Split, CroatiaOpen University of Split School of Medicine in Google Maps