- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05736783
Plyometric and Strength Training of Quadriceps and Hamstrings in Football Players
February 20, 2023 updated by: Riphah International University
Comparative Effects of Plyometric and Strength Training of Quadriceps and Hamstrings on Sprint and Agility Performance in Football Players
Football is a trendy sport in the world.
A typical footballer runs more than 10 kilometers in an average game of 90 minutes.
FIFA regulates the sport of football and the world cup is conducted every 4 years.
Plyometric exercise training uses speed and different forced movements to build muscle power.
Plyometrics training improves physical performance and the ability to do different activities.
Strengthening exercises are designed to increase the strength of specific groups of muscles.
Strengthening exercises overload the muscle until the point of muscle fatigue.
By conducting the study, it will help us to make a better understanding that whether plyometrics or strength training is more effective so that we can cooperate it into the regular exercise of the football player so that their sports performance can be enhanced.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
It will be a randomized clinical trial.
It will be conducted at the Pakistan sports board and coaching center, Lahore.
A sample of 40 athletes will be taken using convenient sampling.
Athletes will be randomly allocated into two groups.
Group A was given plyometrics and group B was given strengthening exercises.
Athletes will be assessed using a 20m sprint test and an Illinois agility test before the initiation of the exercise regimen.
Athletes will perform plyometrics 5 days a week and strength training twice a week for 6 weeks.
Athletes will be reassessed after 6 weeks.
Statistical analysis will be used to determine their effects with the help of the software SPSS 25.
Study Type
Interventional
Enrollment (Actual)
36
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
-
-
Punjab
-
Lahore, Punjab, Pakistan, 5433
- Pakistan Sports Board
-
-
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
15 years to 30 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- the age group of 15-30 years.
- Participants that are practicing five times a week
- Participants having experience of at least 1 year
Exclusion Criteria:
- Athletes with any musculoskeletal injuries;
- Athletes with any systemic illness;
- Novice football players
- Elite/ International players
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: plyometric exercises
performing plyometric exercises for 6 weeks
|
|
Experimental: strenghtening of quadriceps and hamstring
performing strengthening of quadriceps and hamstring for 6 weeks
|
1st to 3rd week l 4th to 6th week Squat 2x12 3x8 l 3x10 4x6 Knee extension 3x12 3x8 l 2x10 2x6 Nordic hamstring 3x3 3x3 l 3x4 3x4
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
20 meter sprint test
Time Frame: 6 weeks
|
20 meter sprint test: a popular test used to determine how fast athlete can run
|
6 weeks
|
Illinois Agility Test
Time Frame: 6 weeks
|
Illinois Agility Test is a commonly used test of agility in sports
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Muhammad Asrar Yousaf, Masters, Riphah International 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)
January 8, 2022
Primary Completion (Actual)
October 1, 2022
Study Completion (Actual)
October 1, 2022
Study Registration Dates
First Submitted
January 22, 2023
First Submitted That Met QC Criteria
February 20, 2023
First Posted (Estimate)
February 21, 2023
Study Record Updates
Last Update Posted (Estimate)
February 21, 2023
Last Update Submitted That Met QC Criteria
February 20, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- REC/RCR&AHS/22/0427
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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