- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06501833
Efficacy of FIFA 11+ Kids Injury Prevention Program on Soccer-specific Skills Among Young Soccer Players
Efficacy of FIFA 11+ Kids Injury Prevention Program on Soccer-specific Skills Among Young Soccer Players- A Randomized Controlled Trial
Background: Soccer is a prevalent sport worldwide; most soccer players are under 18. Soccer has benefits for your health, but there is also a chance that you could get injuries occasionally. High injury rates have been observed in both adult and young players, which has prompted the development of various preventive measures. FIFA recently introduced the FIFA 11+ Kids program for children under 14 to prevent soccer injuries and enhance kids' performance. To date, no studies have been done to determine whether adding the FIFA 11 + kids program for young players under 14 will enhance soccer-specific skills.
Objective: To investigate the efficacy of FIFA 11+ Kids on soccer-specific skills among young soccer players.
Methods: Thirty six young soccer players (aged 7-13) will be assigned randomly to the following groups: the control group (n =18) and the FIFA 11+ Kids program (n = 18). The experimental group will perform eight weeks of FIFA 11+ kids program (3/week). The control group will be instructed to continue their regular training . Three soccer specific skills tests : the Slalom dribble test, Harre circuit test, and Loughborough soccer passing test, will be done before and after eight weeks of training.
Statistical analysis: IBM SPSS software (version 20) will be used for all statistical analyses. Data will be summarized in terms of mean and SD. Normality is checked with the Shapiro-Wilk test and homogeneity with Levene's tests. If the data are normally distributed, a paired t-test will be used for within-group difference comparison, and an independent t-test will be used for between-group comparison. If the data are not normally distributed, the Wilcoxon-Signed rank and Mann-Whitney U tests will be used.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
The inclusion criteria are
- Healthy male young soccer players between the ages of 7-13 (al Attar et al., 2022).
- Playing experience of at least one year.
- Participating in a training session at least three times per week (Teixeira et al., 2021).
- Participating in training at least 4.5 hours a week.
The exclusion criteria:
- Upper or lower limb injuries require medical attention within the last six months (al Attar et al., 2022).
- Any systemic disease, cardiovascular, neurological disorders, or surgery may affect the measurement and participation as reported by the participants (al-Attar et al., 2022).
- Any medication which may affect the training or measurement as reported by the participants.
- Any biomechanical abnormalities as reported by the participants.
- Missed two consecutive training sessions or three separate ones (Mirwald et al., 2002).
Missing one of the testing sessions (Mirwald et al., 2002).
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: FIFA 11+ kids program group
|
The experimental group will perform eight weeks of FIFA 11+ kids program (3/week).
|
|
Active Comparator: Regular training group
|
The control group will be continuing their regular training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Slalom dribble test
Time Frame: pre and immediately post intervention
|
pre and immediately post intervention
|
|
Harre circuit test
Time Frame: pre and immediately post intervention
|
pre and immediately post intervention
|
|
Loughborough soccer passing test
Time Frame: pre and immediately post intervention
|
pre and immediately post intervention
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- IRB-PGS-2023-03-254
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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