The Effectiveness of Calistenic Exercise Training in Adolescents

June 29, 2021 updated by: Nihan Ozunlu Pekyavas, Baskent University

The Effectiveness of Calistenic Exercise Training in Adolescents Receiving Online Education During COVID-19 Pandemic

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.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

38

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ankara, Turkey, 06810
        • Baskent University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

11 years to 14 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: exercise training group
The duration of the study was targeted as 8 weeks. Our trainings consist of 3 sessions per week, with an average of 45 minutes of calisthenic exercises per session. Exercises initially started with an average of 30 minutes, 10 repetitions, gradually increased difficulty once every two weeks, time increased to 45 minutes movements were modified for those who were forced to perform the exercise program. The program was completed with 5 minutes of warm-up and 5 minutes of cooling exercises before exercise training. All exercises were conducted on a video chat platform supervised by an experienced physiotherapist.
these exercises are a kind of exercise for increasing cardiovascular endurance
No Intervention: control group
no exercise was given

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The levels of physical activity
Time Frame: 8 weeks
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
sleep quality
Time Frame: 8 weeks
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
quality of children's lives
Time Frame: 8 weeks
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
the level of anxiety
Time Frame: 8 weeks
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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2021

Primary Completion (Actual)

June 21, 2021

Study Completion (Actual)

June 21, 2021

Study Registration Dates

First Submitted

June 21, 2021

First Submitted That Met QC Criteria

June 21, 2021

First Posted (Actual)

June 29, 2021

Study Record Updates

Last Update Posted (Actual)

July 1, 2021

Last Update Submitted That Met QC Criteria

June 29, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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