- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05811273
Effect of Physical Readiness Training In Badminton Players
Effects of Physical Readiness Training on Speed, Power, and Dynamic Balance in Badminton Players
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Badminton is an extremely demanding sport. At an elite level, players are often required to perform at their limits of speed, agility, flexibility, endurance and strength. On top of all of this, players must maintain a high state of concentration in order to meet the tactical / mental demands of dealing with their opponents. In young badminton players, the most important attributes are high levels of skill. A long-term commitment to endurance training is necessary to reach and maintain a player full physical potential. These are two primary objectives of the endurance program are to prevent injury and enhance the abilities to play the game. Endurance plays the key role in all motor abilities, technical skills and tactical actions. Endurance performance capacity has long been recognized as important prerequisite for on field performance for badminton players.
This study will be a randomized controlled trial in which 28 sample size will be taken. The participants will be allocated into control and experimental group. The sample will be taken from Pakistan Sports Board. Control group will follow their daily warm up activities. Interventional group will follow the physical readiness training. Physical readiness training in experimental group adding following exercises along with their conventional exercises. Bend and Reach:5 repetitions, Rear Lunge:5 repetitions per leg, High Jumper:5 repetitions, Rower:5 repetitions, Squat Bender:5 repetitions, Windmill:5 repetitions, Forward Lunge:5 repetitions per leg, Prone Row:5 repetitions, Bent-Leg Body Twist:5 repetitions per side, Push-Up:5 repetitions. And control group population will continue with their conventional exercises only. These exercises will continue for 4 weeks, 3 days per week. Speed (shuttle run test), Power (vertical jump test), Balance (star excretion test). Comparison of two groups control and interventional be done by applying independent sample t-test and p-value < 0.05 will be taken as significance.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Imran Amjad, PhD
- Phone Number: 03324390125
- Email: imran.amjad@riphah.edu.pk
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 5433
- Recruiting
- Pakistan Sports Borad
-
Contact:
- Amna Shaid, t-DPT
- Phone Number: 03344512823
- Email: amna.shahid@riphah.edu.pk
-
Contact:
- Maria Talat, MS-SPT
- Phone Number: 03320044328
- Email: mariatalat007@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Males
- 7-30 years of age
- playing experience of at least 1 years and has regular practices
Exclusion Criteria:
- Any recent injury that required medical attention;
- Significant musculoskeletal, neurological, visual, vestibular, cardiorespiratory, or cognitive disorders
- players who worked in occupations involving heavy manual work
Study Plan
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: physical readiness training
Bend and Reach:5 repetitions, Rear Lunge:5 repetitions per leg, High Jumper:5 repetitions, Rower:5 repetitions, Squat Bender:5 repetitions, Windmill:5 repetitions, Forward Lunge:5 repetitions per leg, Prone Row:5 repetitions, Bent-Leg Body Twist:5 repetitions per side, Push-Up:5 repetitions.
|
Bend and Reach:5 repetitions, Rear Lunge:5 repetitions per leg, High Jumper:5 repetitions, Rower:5 repetitions, Squat Bender:5 repetitions, Windmill:5 repetitions, Forward Lunge:5 repetitions per leg, Prone Row:5 repetitions, Bent-Leg Body Twist:5 repetitions per side, Push-Up:5 repetitions.
|
|
Active Comparator: control group
general routine exercises
|
general exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Vertical jump test
Time Frame: 4 week
|
The Vertical Jump test is used to evaluate a candidate's lower-body strength. A vertical jump test gauge is used to conduct the test. Applicants should stand with their feet level and hip width apart beneath the testing gauge, with their dominant side closer to the gauge. The person then raises their dominant arm and fingers vertically over their head. On the test gauge, the test assessor then set the applicant's reach height to zero (0). The leap must be done with both feet flat on the ground without taking a step or running up from the starting position. To safeguard their lower limbs, candidates must take off and land with both feet. Only two (2) tries are permitted for applicants who must leap 30cm or greater |
4 week
|
|
Shuttle run test
Time Frame: 4 weeks
|
The Interval Shuttle Run Test started directly after the warm-up.
Subjects were required to run back and forth on a 20-m course with pylons set 3 m before the turning lines.
|
4 weeks
|
|
star excursion balance test
Time Frame: 4 week
|
The SEBT (Standing Excursion Balance Test) evaluates postural control and dynamic balance.
It is currently widely used as a clinical evaluation tool.
SEBT necessitates a combination of lower extremity strength, flexibility, and balance.
This test is useful in determining whether or not a lower extremity athlete is at danger of injury, as well as musculoskeletal disorders in the lower limb, following a training programmed that improves postural control
|
4 week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Amna Shahid, t-DPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
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
- REC/RCR&AHS/23/0407
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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