- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04817280
COVID-19 in Polish Ice Swimmers. (ICE)
Influence of Ice Swimming on Hardening Against SARS-CoV-2 and Influence of AB0 Rh Blood Type on Viral Resistance in Polish Ice Swimmers.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The research tool is an original questionnaire compiled by a team of experts conducting the study. The survey includes questions about sociodemographic data, such as age and gender and blood type in AB0 system with Rh factor, and questions about the frequency of ice swimming, the duration of a single session, and since when respondents have been ice swimming. There was also a question about the respondents' compliance with the restrictions and recommendations related to the pandemic and contacts with people with confirmed SARS-CoV-2 infection. In the survey, researchers ask about the infectious symptoms experienced during the pandemic and about being diagnosed with COVID-19 or its exclusion. People who have been ill are asked about the place of treatment.
The questionnaires are collected in traditional form, on the Internet and as scans of documents. Each survey was completely anonymous. The obtained statistical data will be compared with official data on new COVID-19 cases and recoveries at the same time. Official data are published by the Ministry of Health and earlier also by Sanitary and Epidemiological Stations. The main aim of the study was to determine whether ice swimming also increases resistance to SARS-CoV-2 and COVID-19.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Dolny Slask
-
Wrocław, Dolny Slask, Poland, 51-618
- Department of Public Health at Wroclaw Medical University
-
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Lubuskie
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Gorzów Wielkopolski, Lubuskie, Poland, 66-400
- Department of Radiotherapy of Multidisciplinary Provincial Hospital
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Zielona Góra, Lubuskie, Poland, 65-031
- Treasury Medical Company
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- ice swimmers
Exclusion Criteria:
- not active ice swimmers
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Ice Swimmers Group.
No intervention.
Data obtained from Polish ice swimmers reported by them retrospectively in the questionnaire.
|
The intervention is not made in the course of a research study.
Ice swimming has been introduced earlier by a given group.
The group was made up of people who already swim in ice.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Assessment of the incidence of COVID-19 among ice swimmers compared to the general population.
Time Frame: 47 days.
|
Comparison of the data obtained from surveys collected among ice swimmers with the data published in official channels for the general population during this period.
|
47 days.
|
Assessment of the frequency of asymptomatic SARS-CoV-2 infection among ice swimmers compared to the general population.
Time Frame: 47 days.
|
Comparison of the data obtained from surveys collected among ice swimmers with the data published in official channels for the general population during this period.
|
47 days.
|
Assessment of the frequency of occurrence of particular symptoms of SARS-CoV-2 infection among ice swimmers compared to the general population.
Time Frame: 47 days.
|
Comparison of the data obtained from surveys collected among ice swimmers with the data published in official channels for the general population during this period.
|
47 days.
|
Assessment of the frequency of COVID-19 treatment in an outpatient, inpatient and intensive care unit among ice swimmers compared to the general population.
Time Frame: 47 days.
|
Comparison of the data obtained from surveys collected among ice swimmers with the data published in official channels for the general population during this period.
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47 days.
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Assessment of the impact of parameters and ice swimming strategies on the likelihood of developing COVID-19, the occurrence of individual symptoms of the disease and the severity of its course.
Time Frame: 47 days.
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Inference from data obtained from surveys collected among ice swimmers.
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47 days.
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Assessment of the influence of blood group on susceptibility to SARS-CoV-2 infection among ice swimmers.
Time Frame: 47 days.
|
Inference from data obtained from surveys collected among ice swimmers.
|
47 days.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Assessment of the immunity of the ice swimmer's immune system compared to the general population.
Time Frame: 47 days.
|
Comparison of the data obtained from surveys collected among ice swimmers with the data published in official channels for the general population during this period.
|
47 days.
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Sylwia Sulimiera Michalak, MD, PhD, Department of Pharmacology and Toxicology, Medical University of Zielona Gora
- Study Director: Edyta Wolny-Rokicka, MD, PhD, Department and Center of Radiotherapy, Multidisciplinary Provincial Hospital in Gorzow Wielkopolski
- Study Chair: Andrzej Tukiendorf, Prof., Department of Public Health, Wroclaw Medical University
- Principal Investigator: Lukasz K Wysoczanski, MD, Department of Family Medicine, Wroclaw Medical University
- Principal Investigator: Paulina N Wysoczanska, MD, Department of Family Medicine, Wroclaw Medical University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Pneumonia, Viral
- Pneumonia
- Lung Diseases
- Disease Attributes
- Body Temperature Changes
- Severe Acute Respiratory Syndrome
- COVID-19
- Hypothermia
- Disease Resistance
Other Study ID Numbers
- KB-03/139/2021
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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