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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04942990
Other study ID # KA20/478
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2021
Est. completion date June 21, 2021

Study information

Verified date June 2021
Source Baskent University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objective: The aim of this study is to examine the effectiveness of calisthenic exercise training applied via video chat application on physical activity, physical fitness, quality of life and sleep, and anxiety and depression levels in adolescents during distance education. Material and methods: In our study, 38 adolescents were randomly divided into two equal groups as exercise training group and control group. Calisthenic exercise training was given to the exercise training group for eight weeks, three days a week, via video chat application and under the supervision of a physiotherapist. The control group was evaluated before and after the study period. Physical activity levels of individuals; International Physical Activity Scale, quality of life; Children's Quality of Life Scale, anxiety depression levels; Beck Anxiety Scale, Reynolds Depression Scale and sleep quality were evaluated with Pittsburg Sleep Quality Index.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date June 21, 2021
Est. primary completion date June 21, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 11 Years to 14 Years
Eligibility Inclusion Criteria: - Healthy adolescent children Exclusion Criteria: - Individuals with a disease that could prevent them from doing our exercise training were not included in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
calisthenic exercises
these exercises are a kind of exercise for increasing cardiovascular endurance

Locations

Country Name City State
Turkey Baskent University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Baskent University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary The levels of physical activity International physical Activity Survey: The short form, which has improved Turkish validity and reliability, consists of 7 questions. It provides information about the time spent in severe, moderate walking and sitting activities over the past week. The total calculated energy is calculated as the met spent per minute. 8 weeks
Primary sleep quality The Pittsburgh Sleep Quality Index (PSQI) has been used to assess sleep quality. Applied at start-up and end of 8 weeks. PSQI allows him to identify disturbances in the last month of his sleep. It consists of 24 questions in total. Components are a test that evaluates sleep time, delays in sleep, frequency and severity of sleep-related problems and the impact of poor sleep on the individual's life activity 8 weeks
Primary quality of children's lives Pediatric Quality of life Questionniare Short Form (PedsQL-SF) has been used to measure the quality of children's lives. Developed by Varni and his friends in 1999, Memik conducted a study of the validity and reliability of the scale in 2008. the scale of 23 points is scored in three areas. On the scale, scores and total points are calculated in the areas of emotional functionality, social functionality and school functionality. The scale is scored 0,25,50,75,100 points, equal to 4, 3, 2, 1, 0 respectively. Scale total score, physical health total score is calculated individually and bullet points are collected assessing emotional, social, school functionality, resulting in psychosocial health total score. The higher the points total, the better the quality of life is concluded 8 weeks
Primary the level of anxiety The Beck anxiety Scale was used to determine the level of anxiety. It consists of 21 questions in total. Each item is rated between 0-3 and 4. All points are collected and the higher the score, the higher the anxiety severity. 8 weeks
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