- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05707104
Pilates and Plyometric Training on Physical Performance of Volleyball Players
Comparative Effects of Pilates and Plyometric Training on Physical Performance of Volleyball Players
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This will be a Randomized Clinical Trial that will be conducted at Pakistan Sports Board and Coaching Centre, Lahore. Participants of the study are 38 that will be randomly allocated into 2 groups. The group A will perform Pilates three times per week for 6 weeks and group B will follow Plyometric training three times per week for 6 weeks. Participants of both groups will follow their regular warm up regime and nutrition plans. All participants will undergo a pre and post treatment test via Functional movement's screen test (FMST), vertical-jump test (VJT), 30m sprint test, sit and reach test. The data will be analyzed via SPSS version 21.
Key Words: Performance; Pilates; plyometric; sprint; volleyballVolleyball is one of the famous games which is used in order to enhance and increase physical and game oriented skills in athletes and players. The main goal of athletic training and sports participation is to enhance athletic performance. Different types of training regimes (Pilates and Plyometric) are used on athletes to increase their physical performance. As volleyball is the game of power agility as well as speed. Physical fitness is one of the important parameters of this game. So, Pilates training strengthens the deep core muscles and improves movement, efficiency and muscle control. And plyometric training is to increase the power of subsequent movements using both natural elastic components of muscle and tendon and the stretch reflex. The aim of this study is to compare the effects of Pilates and Plyometric, on physical performance of volleyball players.
This will be a Randomized Clinical Trial that will be conducted at Pakistan Sports Board and Coaching Centre, Lahore. Participants of the study are 38 that will be randomly allocated into 2 groups. The group A will perform Pilates three times per week for 6 weeks and group B will follow Plyometric training three times per week for 6 weeks. Participants of both groups will follow their regular warm up regime and nutrition plans. All participants will undergo a pre and post treatment test via Functional movement's screen test (FMST), vertical-jump test (VJT), 30m sprint test, sit and reach test. The data will be analyzed via SPSS version 21.
Key Words: Performance; Pilates; plyometric; sprint; volleyball
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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PUnjab
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Lahore, PUnjab, Pakistan, 54660
- Pakistan Sports Board
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
• Male and female volleyball players
- Age group 18-30years.
- Participants having an experience of at least 1 year.
- Participants that are practicing for three or more times in a week
Exclusion Criteria:
Athletes with any musculoskeletal injuries;
- Athletes with any systemic illness;
- Novice players
- Any injury within one month
- Players not willing to participate
- Psychologically unstable
- Elite/ International players.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Pilates exercises
performing Pilates exercises three times per week for 6 weeks while maintaining their regular physical activity and nutritional plans.
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NO. Exercises Targeted muscles Repetitions
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EXPERIMENTAL: plyometric exercises
performing plyometric exercises three times per week for 6 weeks while maintaining their regular physical activity and nutritional plans.
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Vertical jump test
Time Frame: 6 week
|
The Vertical Jump test is designed to measure an applicant's lower body strength.
The applicant then crouches and using the arms and legs jumps as high as possible extending the dominant arm.
Upon reaching the top of the jump the applicant must tap the gauge "fins" to mark the jump height.
|
6 week
|
Sit and reach test
Time Frame: 6 weeks
|
The Sit and reach test is one of the linear flexibility tests which helps to measure the extensibility of the hamstrings and lower back.
It was initially described by Wells and Dillon in 1952 and is probably the mostly used flexibility test.
|
6 weeks
|
30m sprint test
Time Frame: 6 weeks
|
The aim of this test is to determine acceleration and speed.The test involves running a single maximum sprint over 30 meters, with the time recorded.
|
6 weeks
|
ILLINOIS AGILITY TEST
Time Frame: 6 weeks
|
The objective of this study is to monitor the athletes development in Agility.
This test the subjects ability to turn in different directions and quickly change speeds.
37
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6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Muhammad Asrar Yousaf, Phd, Riphah International University
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
Keywords
Other Study ID Numbers
- REC/RCR & AHS/22/0430
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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