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The Effect of Wearing Facial Masks on Skin Parameters During the COVID-19 Pandemic

The Effect of Wearing Facial Masks on Skin Parameters During the COVID-19 Pandemic

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05277324
Enrollment
20
Registered
2022-03-14
Start date
2022-03-07
Completion date
2022-05-31
Last updated
2022-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Facial Skin Changes, Skin Condition, Skin Inflammation

Brief summary

The global coronavirus disease pandemic (COVID-19) has led to an increased need to wear protective equipment such as wearing face masks and practicing hygiene measures such as more frequent use of antiseptics. These measures can lead to changes in the skin, the development of new inflammatory skin diseases or exacerbation of existing ones, with health professionals especially under the risk of developing these changes. Changes in facial skin due to wearing masks have been observed in a number of studies, however, part of the study was based solely on subjects' self-assessment or clinical assessment, and only a small part on objective measurements of skin parameters. Also, the impact of prolonged masks' use have not been investigated. The aim of these study was to investigate the effects of constant, long-term use of protective masks on facial skin.

Interventions

OTHERProtective facial mask

Participants, students of health related professions, who wear protective facial mask daily during their internship/practice in health institutions.

Sponsors

University of Split, School of Medicine
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years

Inclusion criteria

* young, healthy volunteers who gave written informed consent - students of health related professions who wear facial mask for at least six hours a day durnig their internship/practice in health care institutions

Exclusion criteria

* skin disease, skin damage on measurement sites * use of corticosteroids, antihistamines and immunomodulators a month prior the inclusion and during the trial * use of emollients three days prior the inclusion in the trial * non-adherence to the trial protocol * exposure to artificial and excessive natural UV radiation * pregnancy and lactation * skin cancer * immunosuppression

Design outcomes

Primary

MeasureTime frameDescription
Transepidermal water loss changeWeekly measurements for the duration of six weeksTewameter will be used to assess skin barrier function as a measurement of the water loss (g/hm2).
Stratum corneum hydration changeWeekly measurements for the duration of six weeksCorneometer will be used to estimate skin dryness. It is a relative measurement and uses arbitrary units (AU).
Skin erythema changeWeekly measurements for the duration of six weeksMexameter will be used to assess erythema. It is a relative measurement and uses arbitrary units (AU).
Melanin content changeWeekly measurements for the duration of six weeksMexameter will be used to assess skin melanin content. It is a relative measurement and uses arbitrary units (AU).
Participants' reported facial skin changesWeekly measurements for the duration of six weeksStructured interview to determine if participants developed adverse events related to mask wearing (such as dryness, erythema, rash, scaling, pruritus, pain/burning, changes in texture or colour, ulcers etc.) between two measurement time-points.
Sebum level changesWeekly measurements for the duration of six weeksSebumeter will be used to assess sebum levels. It is a relative measurement and uses arbitrary units (AU).

Countries

Croatia

Contacts

Primary ContactDario Leskur, PhD, MPharm
dario.leskur@mefst.hr+38521557851

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026