Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06551025
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-08-09
Brief Title:
Comparison of Clinical Parameters in Individuals With Different Physical Activity Levels During the COVID-19 Pandemic Period
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparison of Balance Exercise Capacity Sleep Quality and Coronavirus Phobia in Individuals With Different Physical Activity Levels During the COVID-19 Pandemic Period
Status:
COMPLETED
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The COVID-19 pandemic started in China towards the end of 2019 and soon affected the whole world Restriction and isolation measures have been taken to prevent the spread of this disease caused by a new type of coronavirus coronavirus-2 These measures have changed peoples physical activity levels and have also affected other parameters that physical activity affects This study aims comparison of clinical parameters in with different physical activity levels during the COVID-19 pandemic period
Detailed Description:
In our study the investigators aimed to compare balance exercise capacity sleep quality and coronavirus phobia levels and investigate the relationship between exercise capacity and balance in individuals with different physical activity levels during the COVID-19 pandemic period
Materials and Methods of the Research
The place of study Cardiopulmonary Rehabilitation Unit of Hacettepe University Faculty of Physical Therapy and Rehabilitation
Time of the study It is planned to collect data and write the study between February 2021 and February 2022
Research Population Sample Research Group
The population of the study is healthy individuals whose physical activity level was determined according to the results of the International Physical Activity Questionnare IPAQ
The sample of the study is healthy individuals whose physical activity level is inactive and minimallyheavily active according to the results of the International Physical Activity Questionnare IPAQ
Study Design
Individuals meeting the inclusion criteria will be included in the study The study will be conducted with people between the ages of 18-65 and whose local language is Turkish A total of 64 participants 32 inactive and 32 minimallyheavily active will be included in the study
Evaluations will be made using tele-assessment methods not face-to-face due to the COVID-19 pandemic Verbal informed consent will be obtained from all subjects by video interview method that they voluntarily participated in the study Written informed consent will be obtained from the cases whose verbal consent has been obtained
Inclusion Criteria
Being between the ages of 18-65
Being able to cooperate with the tests
Not have any known acute or chronic health problems that may prevent them from performing the tests or affect the test performance
Not having any known acute or chronic disease that may affect the balance status
Not having orthopedic neurological and serious cardiovascular problems that will affect the performance of the sit-stand test for 1 minute
Volunteering to participate in the study
Having access to a phone or video conferencing platform with a reliable internet connection with their own device
To have the ability to operate these devices independently or with the help of another individual
Have adequate hearing function and language knowledge
Be able to move independently and safely even with walking aid
Exclusion Criteria
Not cooperating with the tests
Known information that may prevent it from performing tests or affect test performance have acute and chronic health problems
Known acute and chronic illness that may affect balance
Have angina and ischemic heart disease onset at rest or with minimal effort
Have a cognitive impairment
Risk of falling and having poor balance Not having access to a phone or video conferencing platform with a reliable internet connection with their own device
Not having sufficient hearing function and language knowledge
Not being able to move independently and safely even with walking aid
Not being willing to participate in the study
Materials and Methods of the Research
The place of study Cardiopulmonary Rehabilitation Unit of Hacettepe University Faculty of Physical Therapy and Rehabilitation
Time of the study It is planned to collect data and write the study between February 2021 and February 2022
Research Population Sample Research Group
The population of the study is healthy individuals whose physical activity level was determined according to the results of the International Physical Activity Questionnare IPAQ
The sample of the study is healthy individuals whose physical activity level is inactive and minimallyheavily active according to the results of the International Physical Activity Questionnare IPAQ
Study Design
Individuals meeting the inclusion criteria will be included in the study The study will be conducted with people between the ages of 18-65 and whose local language is Turkish A total of 64 participants 32 inactive and 32 minimallyheavily active will be included in the study
Evaluations will be made using tele-assessment methods not face-to-face due to the COVID-19 pandemic Verbal informed consent will be obtained from all subjects by video interview method that they voluntarily participated in the study Written informed consent will be obtained from the cases whose verbal consent has been obtained
Inclusion Criteria
Being between the ages of 18-65
Being able to cooperate with the tests
Not have any known acute or chronic health problems that may prevent them from performing the tests or affect the test performance
Not having any known acute or chronic disease that may affect the balance status
Not having orthopedic neurological and serious cardiovascular problems that will affect the performance of the sit-stand test for 1 minute
Volunteering to participate in the study
Having access to a phone or video conferencing platform with a reliable internet connection with their own device
To have the ability to operate these devices independently or with the help of another individual
Have adequate hearing function and language knowledge
Be able to move independently and safely even with walking aid
Exclusion Criteria
Not cooperating with the tests
Known information that may prevent it from performing tests or affect test performance have acute and chronic health problems
Known acute and chronic illness that may affect balance
Have angina and ischemic heart disease onset at rest or with minimal effort
Have a cognitive impairment
Risk of falling and having poor balance Not having access to a phone or video conferencing platform with a reliable internet connection with their own device
Not having sufficient hearing function and language knowledge
Not being able to move independently and safely even with walking aid
Not being willing to participate in the study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None