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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06145386
Other study ID # Pamukkale Universityy
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date February 21, 2022
Est. completion date May 30, 2024

Study information

Verified date April 2024
Source Pamukkale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study; to examine the effects of aerobic and strength training on physical activity level, quality of life and anxiety-stress disorder in young adults with and without COVID-19. In this context, the study was planned by including 15 participants between the ages of 18-25 who had COVID-19 and 15 who did not have COVID-19. Data were collected by applying the Personal Data Form, IPAQ (International Physical Activity Form), SF-36 Quality of Life Scale, Coronavirus Anxiety Scale (CCS), Respiratory Function Tests (PFT), Six Minute Walk Test (6MWT). Aerobic training and strengthening training were applied to people with and without COVID-19 for 12 weeks. Aerobic exercise (walking) was given for 40 minutes 5 days a week, with the target heart rate being 70% of the age-corrected maximum heart rate. Strengthening exercises were applied to the upper (triceps, biceps, deltoid, pectorals) and lower (quadriceps, hamstring, gastrocnemius, tibialis anterior, hip adductors, hip flexors, hip extensors) extremities and back muscles (trapezius, latissimus dorsi) with theraband (resistance band). Significance test of the difference between two means in comparing independent group differences when parametric test assumptions are met for statistical analysis in line with the data collected from the participants; When parametric test assumptions are not met, Mann Whitney U test is used to compare independent group differences, while when parametric test assumptions are met to examine dependent group differences, the significance test of the difference between the two spouses is used; When parametric test assumptions were not met, the Wilcoxon paired two sample test was used. In all analyses, p < .05 was considered statistically significant.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 30
Est. completion date May 30, 2024
Est. primary completion date April 21, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: - Volunteering to participate in the study, - Able to communicate, without hearing and/or visual impairment, - Being between the ages of 18-25 - Not having a systemic disease - Having had COVID-19 in the last 6 months to be included in the study group Exclusion Criteria: - Unable to communicate, hearing and/or visually impaired, - Not being between the ages of 18-25 - Having a systemic disease other than COVID-19 infection, - Having had COVID-19 more than 6 months ago.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Aerobic Exercise and Strength Training
Aerobic Exercise and Strength Training on Physical Activity Level, Quality of Life and Anxiety-Stress Disorder in Young Adults With and Without Covid-19

Locations

Country Name City State
Turkey Istanbul Aydin University Istanbul Kücükcekmece

Sponsors (1)

Lead Sponsor Collaborator
Pamukkale University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary International Physical Activity Questionnaire Used to define participants physical activity level 5 minute
Primary SF-36 Used to indicate the health status of participants 10 minute
Primary Coronavirus Anxiety Scale Used to evaluate experience some psychological problems such as anxiety and depression depends on COVID-19 1 minute
Primary Respiratory Function Tests Used to evaluation of the respiratory system 5 minute
Primary The 6 Minute Walk Test Used to assess aerobic capacity and endurance 6 minute
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