- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06472687
Efects of FIFA 11+Warm-Up Program on Agilitiy, Balance And Proprioception Parameters in The Professional Football Players
June 24, 2024 updated by: Elif Tuğçe Çil, Yeditepe University
This study aimed to compare the effects of the FIFA 11+ warm-up program with a traditional warm-up on agility, balance, and proprioception in professional football players aged 18-30.
Forty-four players were randomly assigned to either the FIFA 11+ group, which performed the program for 10 weeks, or the control group, which continued their usual warm-up routine.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
44
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
-
-
Maltepe
-
Istanbul, Maltepe, Turkey, 34770
- Elif Tuğçe
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- being 18-30 years, individuals who currently play professional football and actively participate in training and matches,
- participants with at least two years of professional football coaching experience,
- no history of any medical conditions that would hinder their ability to perform the required exercises.
Exclusion Criteria:
- a history of musculoskeletal surgery and fractures in the lower extremities,
- a history of acute injury to the musculoskeletal structures of other lower extremity joints in the last three months, affecting joint integrity and function and causing interruption of the desired physical activity for at least one day
- having a history of balance and vestibular disorders were excluded from 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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: FIFA 11+ training group (FTG)
The participants recruited in the FIFA 11+ training group (FTG) and control group (CG) received different warm-up program twice a week for ten weeks.
The FTG received the FIFA 11+ training program and the CG received standard warm-up protocol.
All subjects received the initial participant education and training program instruction.
All training protocols were continued for twice weekly.
The same physiotherapist applied FIFA 11+ training protocol.
|
FIFA 11+ warm-up training program was applied to the experimentel group.
control group (CG) did their usual warm-up program.
|
|
Active Comparator: control group (CG)
The participants recruited in the FIFA 11+ training group (FTG) and control group (CG) received different warm-up program twice a week for ten weeks.
All subjects received the initial participant education and training program instruction.
All training protocols were continued for twice weekly.The same physiotherapist applied FIFA 11+ training protocol.
The control group performed the usual warm-up, which only included running, static and dynamic stretching.
|
exercise training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Agility
Time Frame: Baseline assesment (Begining of the warm-up program), 10th week assessment (through FIFA 11+ program is completed.)
|
Agility was assessed by the Illinois T test
|
Baseline assesment (Begining of the warm-up program), 10th week assessment (through FIFA 11+ program is completed.)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance
Time Frame: Baseline assesment (Begining of the warm-up program), 10th week assessment (through FIFA 11+ program is completed.)
|
The Y balance test is used to evaluate dynamic balance.
|
Baseline assesment (Begining of the warm-up program), 10th week assessment (through FIFA 11+ program is completed.)
|
|
Proprioception
Time Frame: Baseline assesment (Begining of the warm-up program), 10th week assessment (through FIFA 11+ program is completed.)
|
Proprioception was assessed the ability to reposition the knee at 30, 45, and 60 degrees for both the player's right and left leg.
|
Baseline assesment (Begining of the warm-up program), 10th week assessment (through FIFA 11+ program is completed.)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
October 1, 2023
Primary Completion (Actual)
February 1, 2024
Study Completion (Actual)
March 1, 2024
Study Registration Dates
First Submitted
June 17, 2024
First Submitted That Met QC Criteria
June 24, 2024
First Posted (Actual)
June 25, 2024
Study Record Updates
Last Update Posted (Actual)
June 25, 2024
Last Update Submitted That Met QC Criteria
June 24, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- hamed
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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