- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06919146
After-school Game-Based Physical Activity Program Improves Physical Fitness of 9-10-Year-Old Children (AGPAP)
April 7, 2025 updated by: Elvin Onarici Gungor
A 12-week Afterschool Game-Based Physical Activity Program Improves Physical Fitness of 9-10-Year-Old Children: A Randomized Controlled Study
This study investigates the effect of an afterschool game-based physical activity program (AGPAP) on children's PF.
This study was randomized controlled trial involving 120 children from a state school in Eskisehir/Turkey.
The CONSORT checklist was used in this study.
The sample of 9-10 years children (n = 120) was divided into groups by randomization.
The intervention consisted of AGPAP.
For PF, handgrip strength, curl-ups, sit-and-reach, standing long jump, and 10-meter running speed tests were applied.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
130
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
-
-
Eski̇şehi̇r
-
Odunpazari, Eski̇şehi̇r, Turkey, 26160
- Eskisehir Tecnical 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
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- being 9-10-year-old,
- volunteering,
- permission from the child's parents,
- not having any amputations or permanent disabilities in their bodies,
- not having chronic or acute diseases,
- not using a support device.
Exclusion Criteria:
- any discomfort during measurements,
- the child does not want to participate in the measurement,
- the child does not participate in the practices due to any disability or discomfort,
- not reaching 80% participation in the program.
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
EG additionally participated in AGPAP (4:00 pm-5:00 pm) twice a week, every Wednesday and Friday, for a total of 60 minutes, for 12 weeks.
AGPAP started the week after the pre-tests for EG.
The intervention program consisted of 24 traditional street games, including running, hopping, galloping, leaping, jumping, sliding, striking, catching, ball catching, overhand throwing, balance, one-hand throwing, flexibility, coordination, shooting at the target, and hand-arm-leg strength and both outdoor and indoor facilities were utilized based on whether conditions.
Each practice phase is 60 minutes long and includes three stages: instruction and warm-up (10 min.),
AGPAP practice (45 min.),
and cooling-down (5 min.).
Two researchers who hold graduate degrees in physical education and sport led AGPAP and recorded children's participation.
At the end of the intervention, the same testing procedures and testing materials were used for post-test measurements.
|
EG participated in AGPAP (4:00 pm-5:00 pm) twice a week, every Wednesday and Friday, for a total of 60 minutes, for 12 weeks.
EG and CG did not participate in any additional physical activity programs after-school.
|
|
No Intervention: Control
Measurements were applied to the CG
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Mass Index
Time Frame: 12 weeks
|
Body weights were measured using a digital scale (SECA, Hamburg) with an accuracy of 0.1 kg while subjects were wearing as light clothing as possible and barefoot.
Heights were measured using a portable stadiometer (SECA, Hamburg) with an accuracy of 0.1 cm while subjects were barefoot, with their feet together and their heads on a horizontal plane 47.
The weight(kg)/height2(m) formula was used to calculate BMI.
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Handgrip strength test
Time Frame: 12 weeks
|
The hand grip strength test measures the explosive power of the upper body using an adjustable and calibrated hand dynamometer (Takei, Tokyo, Japan).
Participants were asked to hold them in their right and left hands and squeeze it slowly and continuously until they reached the max.
for at least 2 s.
The best of 2 repetitions was recorded as the test score in kg.
|
12 weeks
|
|
Standing long jump test
Time Frame: 12 weeks
|
Each participant attempted to jump as far as possible across a certain distance while standing, with their arms forward, their feet closed, and landing on the ground.
The best of the 2 attempts was recorded in centimeters.
|
12 weeks
|
|
Curl-ups test
Time Frame: 12 weeks
|
Participants were asked to lie with their arms crossed on their chest, their knees bent, and their feet flat on the floor.
Afterward, they were asked to lift their upper bodies with their elbows facing forward, touch their knees, and then return to the lying position.
The total number of complete curl-ups performed correctly in 30 seconds was recorded.
|
12 weeks
|
|
The sit and reach test
Time Frame: 12 weeks
|
The sit and reach tests were applied using a specially constructed box that had a slide runner attached to the top.
The accuracy of the instrument used was 0.1 cm, and the length it was able to measure was 80 cm (01285A, Lafayette, USA).
Subjects sat on a flat surface with their back, shoulders, and the back of their head close to the wall for the sit-and-reach test.
Their arms were straightened, their hands were placed on the tester board with palms facing down, and their legs were positioned straight.
Each participant placed their hands side by side on the measurement starting line on the bench and gradually pushed the bar on the sit-and-reach bench forward to the furthest point they could while reaching with their hands without bending their knees.
Each participant repeated the test two times, and the best of these two repetitions was taken into statistical evaluation.
|
12 weeks
|
|
10-meter running speed test
Time Frame: 12 weeks
|
Photocells were placed at the beginning and end of the 10-meter track (Smart Speed, Fusion Sport, Brisbane, Australia).
Participants waited in a standing starting position 50 cm behind the starting line and started sprinting upon receiving the command when they were ready.
Two repetitions were conducted, and the best result was recorded at the end of the trials.
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: ELVİN ONARICI GÜNGÖR, dr, Eskisehir Tecnical University
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)
July 1, 2020
Primary Completion (Actual)
August 27, 2020
Study Completion (Actual)
December 7, 2020
Study Registration Dates
First Submitted
March 12, 2025
First Submitted That Met QC Criteria
April 7, 2025
First Posted (Actual)
April 9, 2025
Study Record Updates
Last Update Posted (Actual)
April 9, 2025
Last Update Submitted That Met QC Criteria
April 7, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- EskisehirTU-SBF-EOG-01
- Eskisehir Technical University (Other Identifier: Education)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
only IPD used in the results publication
IPD Sharing Time Frame
January 2025-January 2026
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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.
Clinical Trials on Physical Activity
-
Muğla Sıtkı Koçman UniversityEge UniversityCompletedPhysical Activity | Physical Activity Behavior | Physical Activity LevelsTurkey
-
Istinye UniversityCompletedPhysical Activity | Youth | Physical Activity Barriers | Physical Activity FacilitatorsTurkey
-
University of ManitobaResearch ManitobaCompletedPhysical Activity | Physical Activity Self-Definition
-
Universidad Pedagogica Nacional, ColombiaEnrolling by invitationPhysical Activity | Running | Running Performance | Running Endurance | Physical Activity in Adults | Physical Activity IntensityColombia
-
Istanbul Kültür UniversityWithdrawnPhysical Activity Level | Physical Activity Awareness
-
Universidade do PortoActive, not recruitingPhysical Activity | Physical Fitness | Well BeingPortugal
-
Odense University HospitalUniversity of Southern DenmarkRecruitingQuality of Life | Physical Activity | Physical Disability | Physical Function | ParticipationDenmark
-
Firat UniversityNot yet recruitingUniversity Students | Physical Activity Level | Postural Awareness | Physical Activity AttitudeTurkey
-
Georgetown UniversityUniversity of PennsylvaniaCompletedPhysical Activity | Motor ActivityUnited States
-
Pham Ngoc Thach University of MedicineCompletedModerate Physical Activity (MPA) | Vigorous Physical Activity (VPA) | Moderate to Vigorous Physical Activity (MVPA) | Total of Sleep Time (TST)Vietnam
Clinical Trials on Physical Activity
-
Health Education Research Foundation (HERF)CompletedQuality of LifePakistan
-
Zohra Institute of Health SciencesCompletedPhysical Activity and StressPakistan
-
University GhentCompleted
-
Centre Hospitalier Universitaire DijonWithdrawn
-
Fundacion para la Investigacion y Formacion en...CompletedImpaired CognitionSpain
-
Universidad Santo TomasEmory University; Universidad Pública de Navarra; Universidad de Granada; University... and other collaboratorsCompletedObesity | Lipid Metabolism Disorders | Mental Health Wellness 1 | Body Composition, Beneficial | Metabolic Syndrome X
-
AUSL Romagna RiminiFondazione IRCCS Istituto Nazionale dei Tumori, MilanoRecruitingNon-Small Cell Lung CancerItaly
-
Centre Hospitalier Departemental VendeeTerminated
-
Fundación para la Investigación del Hospital Clínico...CompletedObesity | Severe Mental Disorder
-
Augusta UniversityNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Kansas... and other collaboratorsCompletedMental Disorders, SevereUnited States