The Investigation Of Exercise Capacity And Exercise-Induced Fatigue in Young Adults Who Survived From Coronavirus
NCT ID: NCT04864132
Last Updated: 2022-11-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
60 participants
OBSERVATIONAL
2021-05-27
2022-11-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Subjects survived from COVID-19
The subjects who had confirmed COVID-19 infection aged between 18-30/years
6-minute walk test
This test assesses submaximal exercise capacity.
Incremental shuttle walk test
This test assesses maximal exercise capacity.
Subjects never had COVID-19
The subjects aged between 18-30/years who have not been diagnosed with COVID-19 as of March 11of 2020 and who have not been in contact and risky according to the "Life Fits Into Home" application
6-minute walk test
This test assesses submaximal exercise capacity.
Incremental shuttle walk test
This test assesses maximal exercise capacity.
Interventions
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6-minute walk test
This test assesses submaximal exercise capacity.
Incremental shuttle walk test
This test assesses maximal exercise capacity.
Eligibility Criteria
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Inclusion Criteria
Confirmed COVID-19 infection - For healthy individuals of the same age group who have not had COVID-19: Individuals who have not been diagnosed with COVID-19 as of March 11, 2020 and who have not been in contact and risky according to the "Life Fits Into Home" application
\- For all participants; Answering "No" to all questions in the Physical Activity Readiness Questionnaire.
Exclusion Criteria
* Individuals with a fever\> 38 ° C and / or resting blood pressure \<90/60 mmHg or\> 140/90 mmHg and/or oxygen saturation ≤95%,
* Individuals who have been involved in a physiotherapy and rehabilitation program within the last 3 months,
* Individuals with insufficient cooperation
* Individuals with blood coagulation disorders contraindicated for blood lactate analysis,
* Pregnant women or individuals with suspected pregnancy
18 Years
30 Years
ALL
Yes
Sponsors
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Biruni University
OTHER
Responsible Party
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Buket AKINCI
Associated Proffesor
Principal Investigators
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Buket Akinci, Assoc. Prof.
Role: STUDY_CHAIR
Biruni University
Zeynep Hosbay, Assoc. Prof.
Role: PRINCIPAL_INVESTIGATOR
Biruni University
Locations
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Biruni University
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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2015-KAEK-47-21-03
Identifier Type: -
Identifier Source: org_study_id
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