- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04375410
Consequences of Intensified Handwash and Hand Disinfection Among Children During the COVID19 Pandemic
March 30, 2021 updated by: Tine Caroc Warner, Vendsyssel Hospital
Re-opening of the Country and Dermal Consequences of Mandatory Intensified Handwash and Hand Disinfection Among a Danish Pediatric Population During the COVID19 Pandemic
During the COVID-19 pandemic after reopening of the country, school, kindergarten and daycare, children have been obligated to do frequent handwash.
The study group wished to investigate whether this has had implications on symptoms of dry, red, itchy or sore hands and hand eczema.
The investigation was performed within the first and second week after reopening by questionnaires distributed to parents electronically via schools, kindergartens and daycare facilities electronic platforms.
Study Overview
Status
Completed
Conditions
Detailed Description
During the COVID-19 pandemic Denmark closed down, including schools, kindergartens and daycare.
After reopening of the country 5 weeks later obligatory frequent handwash was a requirement from the government and routines has been implemented at all reopened schools, kindergartens and daycare.
The study group wished to investigate whether this has had implications on symptoms of dry, red, itchy or sore hands and hand eczema.
Also the study group wished to investigate if frequency or use of hand disinfection mattered.
The investigation was performed within the first and second week after reopening by questionnaires distributed to parents electronically via schools, kindergartens and daycare electronic platforms.
The questionnaire included 20 questions on demographics, frequency of hand wash and use of disinfectants, current and previous symptoms of eczema, atopic dermatitis and dispositions.
Study Type
Observational
Enrollment (Actual)
6273
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Nordjylland
-
Hjørring, Nordjylland, Denmark, 9800
- Tine Caroc Warner
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 second to 13 years (CHILD)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Children i Hjoerring, Aalborg, Rebild or Skanderborg municipaility
Description
Inclusion Criteria:
- All children returned to daycare, kindergarten or school after covid19 close down of the country
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dermal reaction to frequent hand wash and disinfection in children
Time Frame: 9 days
|
Dermal symptoms as a result of frequent hand wash and disinfection among children
|
9 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Soeren Haghstroem, M.D, PhD, Aalborg University Hospital, Aalborg University
- Principal Investigator: Luise Borch, M.D, PhD, Regional Hospital West Jutland, Herning
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
April 22, 2020
Primary Completion (ACTUAL)
April 30, 2020
Study Completion (ACTUAL)
May 10, 2020
Study Registration Dates
First Submitted
April 30, 2020
First Submitted That Met QC Criteria
May 1, 2020
First Posted (ACTUAL)
May 5, 2020
Study Record Updates
Last Update Posted (ACTUAL)
April 1, 2021
Last Update Submitted That Met QC Criteria
March 30, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SH042020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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