- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05261958
Effect of Speed,Agility and Quickness Training on Technical Skills in Football Players
April 15, 2022 updated by: Riphah International University
Effect of Speed, Agility and Quickness Training on Technical Skills in Football Players
The study is designed to determine the effectiveness of Speed, Agility and Quickness training on technical skills in football players
Study Overview
Detailed Description
Football is a fast-paced, dynamic sport that requires expert movements.
The goal of the game is to outscore your opponent in terms of goals scored.
Players must perform a variety of expert movements, both with and without the ball, to achieve this goal.
'The learned ability to bring about predetermined results with utmost assurance, frequently with the least investment of time or energy or both,' according to an initial definition of talent.
'The constant output of goal-oriented movements, which are taught and unique to the job,' according to a more modern definition of competence.
It is critical for players to have the fundamental motor abilities, such as running, agility, and acceleration, in order to learn and execute soccer skills effectively.
Fundamental motor skills are seen as essential precursors or related factors to technical skills and therefore excellence in soccer.Furthermore, through a variety of soccer-specific activities, the SAQ training system consolidates speed, agility, and quickness.
All exercises are carried out with appropriate biomechanical movement structures, resulting in significant energy and time savings.
Aside from major abilities, power performance necessitates optimal joint mobility, dynamic balance, an appropriate locomotors system, and energy generation, among other things.
Study Type
Interventional
Enrollment (Actual)
50
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
-
-
ICT
-
Islamabad, ICT, Pakistan, 44000
- Riphah International 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
18 years to 25 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Male players
- Age group of 18 years to 25 years.
- The study includes players, who are playing form 6 months to 1 year.
Exclusion Criteria:
- Players with any disability
- Injured players
- Players with psychological issues
- Players who are on any sort of medication
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Interventional Group
|
interventions listed above were applied on the players which will improve running mechanics and impove speed power and agility in football players
Other Names:
|
No Intervention: Control Group
Players in this group did not undergo any interventional Programme rather than their daily routine work which includes:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Shuttle Run test
Time Frame: 6 weeks
|
Agility Shuttle Run is a test of agility, in which the participant runs back and forth between two parallel lines as fast as possible, picking up blocks of wood, for a total of 120 ft.
A shuttle run time below four seconds is generally considered great, with the best players closer to the 3.8-second range, the total time is 4 seconds.
|
6 weeks
|
12 min run test
Time Frame: 6 weeks
|
Place markers at set intervals around the track to aid in measuring the completed distance.
Participants run for 12 minutes, and the total distance covered is recorded.
|
6 weeks
|
Speed
Time Frame: 6 weeks
|
Set out a series of markers in a straight line at 0, 10, 20 and 30m.
The player taking the test stands at the start, and the person timing stands on the 10m mark.
On command, the player sprints through the 10m mark and the timer records the time they pass the marker.
Repeat for 10m, and then do twice for 20m and 30m.
|
6 weeks
|
Vertical jump
Time Frame: 6 weeks
|
The simplest method to measure an athlete's vertical jump is to get the athlete to reach up against a flat wall, with a flat surface under his/her feet and mark off the highest point he/she can reach flat-footed
|
6 weeks
|
Mcdonald Soccer skill test
Time Frame: 6 weeks
|
A soccer ball is placed on a line, marked 9 feet from the wall.
On the signal, "Go," the player kicks the ball against the wall as many times as possible in 30 seconds.
The test score is the highest total of any three trials.
|
6 weeks
|
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)
June 29, 2021
Primary Completion (Actual)
October 31, 2021
Study Completion (Actual)
November 1, 2021
Study Registration Dates
First Submitted
February 20, 2022
First Submitted That Met QC Criteria
February 20, 2022
First Posted (Actual)
March 2, 2022
Study Record Updates
Last Update Posted (Actual)
April 18, 2022
Last Update Submitted That Met QC Criteria
April 15, 2022
Last Verified
April 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- REC/01023/Sajjad Ali
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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