- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06446375
FIFA 11+ Kids Training Protocol and Physical Performance
Effects of FIFA 11+ Kids Training Protocol on Motor Competence and Physical Performance in Youth Female Volleyball Players: A Randomized Controlled Trial
This study evaluates the FIFA 11+ Kids Training Protocol, specifically its application to young female volleyball players. It compares it against standard warm-up routines in terms of enhancing motor skills and physical performance. The research anticipates that the FIFA 11+ principles will yield positive outcomes when integrated with existing knowledge of volleyball performance metrics. The study involved 34 young female volleyball players divided into an exercise group (15 players) and a control group (19 players). Initial assessments included anthropometric measurements and motor competence tests such as balancing backward, jumping sideways, moving sideways, and eye-hand coordination (KTK3+ tests).
Subsequent sessions focused on physical and functional tests, including balance performance, agility (pro-agility test), vertical jump (countermovement jump test), and the functional movement screen (FMS) test. A two-way analysis of variance was used to compare the effects of the exercise versus the control group over time, revealing that the exercise group showed significant improvements in dynamic balance, KTK balancing backward, and KTK moving sideways. This study aims to provide innovative insights into the effectiveness of the FIFA 11+ Kids Training Protocol, highlighting its potential benefits in improving physical and motor competencies in young female volleyball players.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Riyadh, Saudi Arabia, 12341
- Monira Aldhahi
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Children between age of 11 -13 years old
- typically developing children
- participants should not be using any medication
- Free of any history of cardiovascular disease
Exclusion Criteria:
- Intake of performance-enhancing drugs, anabolic steroids
- Any history of injury, or physiological or physical limitations that could affect the ability to perform training and physical testing in the last year.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: The experimental Group
FIFA 11+ KIDS Training Protocol will be conducted by the experimental group twice a week for 8 weeks with 15-20-minute interventions.
Volleyball players continued their standard volleyball training after the training protocol.
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FIFA 11+ KIDS Training Protocol consists of seven different exercises: three for unilateral, dynamic stability of the lower limbs (hopping, jumping and landing); three for whole body and trunk strength/stability; and one exercise on falling technique.
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Active Comparator: Control Group
The control group will continue their regular volleyball training interventions.
All tests were conducted at the same time of day (13:30-16:30) to minimize the impact of circadian rhythms on the results.
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Regular physical activity
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Body coordination test
Time Frame: at baseline and end of 8 week
|
The Body coordination test for children (KTK3+ test battery, supported by a hand-eye coordination task), will be used to assess children's motor competence.
KTK3 measures general gross motor coordination .
The test include backward balancing (BB), sideways movement (MS), sideways jumping (JS), and hand-eye coordination task (EHC).
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at baseline and end of 8 week
|
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Pro-agility test
Time Frame: at baseline and end of 8 week
|
The test course set with markers placed 5 yards (4.57m) to the left and right of the starting line, with indicators (motivational for the participants' age) placed accordingly.
A photocell gate was placed at the starting line to record repeated passage times.
Before the start of the application, the participant took their position at the starting line.
When ready, they touched the marker on the right first, then the marker on the left, and finally crossed the starting line to finish the test.
Measurements will be conducted in two trials.
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at baseline and end of 8 week
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Functional Movement Screen Test Protocol
Time Frame: at baseline and end of 8 week
|
The Functional Movement Screening (FMS)™ system, developed by Gray Cook, Lee Burton and Keith Fields, is a system used to determine potential injury risk in athletes and the quality of individuals' movement patterns, to assess poor neuromuscular control and to improve athletic performance.
The Functional Movement Screening test consists of 7 different basic movements (deep squat, hurdle step, single line step, shoulder mobility, active straight leg raise, trunk stability push-up, rotation stability).
Scoring for FMS consists of four different possibilities.
Scores range from zero to three, with three being the best possible score.
The maximum score for the FMS test is 21.
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at baseline and end of 8 week
|
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Peak power and jump height measurement
Time Frame: at baseline and end of 8 week
|
Countermovement Jump (CMJ) values of all participants will be measured.
Peak muscle power measures in watts (W) using portable force platform system (peak power2.0,
USA).
The measurement frequency of the device was set to 500 Hz.
Participants will undrergo a 10-minute warm-up program before completing a CMJ.
Participants will be asked to begin a downward movement and jump as high as possible after hearing a tone from the computer.
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at baseline and end of 8 week
|
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Balance tests
Time Frame: at baseline and end of 8 week
|
Static and dynamic balance parameters were assessed using a mobile platform that provides an interactive training tool.Participants performed measurements of static and dynamic balance parameters on the mobile platform for 30 seconds in two trials.
The highest score from the two trials was used in the statistical analysis.
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at baseline and end of 8 week
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Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2023.48.03.07
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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