- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06212843
Effect of 8 Week Plyometric Training on Injury Prevention in Domestic Cricket Players
January 18, 2024 updated by: Riphah International University
The study aims to find the effectiveness of plyometric training on injury prevention of domestic cricket players.
Players will be taken from Chakwal and a well designed plyometric plan will be implied on them for 8 weeks.
After that the results will be compared with the other group who did not get any plyometric training to see the effectiveness of the treatment plan.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
26
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 Contact
- Name: Waqar Awan, PHD
- Phone Number: 0333-534884
- Email: waqar.ahmed@riphah.edu.pk
Study Contact Backup
- Name: Aqsa Safdar, DPT
- Phone Number: 03054585552
- Email: aqsa.safdar888@gmail.com
Study Locations
-
-
Punjab
-
Islamabad, Punjab, Pakistan, 44600
- Recruiting
- Riphah International University
-
Contact:
- Waqar Ahmed, PHD
- Phone Number: 0333-5348846
- Email: waqar.ahmed@riphah.edu.pk
-
Contact:
- Aqsa Safdar, DPT
- Phone Number: 03054585552
- Email: aqsa.safdar888@gmail.com
-
-
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:
- domestic cricket players between 18-25 years.
- actively engaged for more than 1 year
Exclusion Criteria:
- history of trauma/injury in last month
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group A (Plyometric training)
|
The group will receive plyometric exercises in a controlled environment. Following Plyometrics would be performed.
|
|
Other: Group B (Conventional)
|
The group will receive conventional exercises in a controlled environment. Following conventional exercises would be performed.
5.Squats |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Deep squat Test
Time Frame: 8 weeks
|
The deep squat test typically involves a qualitative assessment rather than a numerical score.
Trained evaluators observe the individual's form during the squat, looking for deviations such as heels lifting, knees collapsing, or torso leaning forward.
A smooth, controlled movement with proper alignment is considered optimal.
Interpretation involves identifying any biomechanical issues, muscle imbalances, or flexibility limitations based on observed deviations.
This qualitative information guides fitness professionals, coaches, or healthcare providers in tailoring corrective exercises or interventions to address specific movement patterns or limitations identified during the deep squat test.
|
8 weeks
|
|
One legged squat
Time Frame: 8 weeks
|
The one-legged squat, also known as the single-leg squat or pistol squat, is a functional movement exercise that challenges lower body strength, balance, and flexibility.
In this exercise, an individual stands on one leg while lowering their body into a squat position and then returning to the starting position.
Scoring typically involves assessing the ability to maintain balance, depth of the squat, and overall control during the movement.
Interpretation focuses on identifying any asymmetries, weaknesses, or compensations in the lower body, helping tailor specific exercises or interventions to improve strength and stability in the individual's functional movement patterns.
|
8 weeks
|
|
Inline lunges
Time Frame: 8 weeks
|
The inline lunge is a functional movement assessment used to evaluate lower body flexibility, balance, and symmetry.
In this exercise, an individual steps forward into a lunge position along a straight line, assessing the ability to maintain proper alignment and stability.
Scoring involves observing the quality of the lunge, noting any deviations or asymmetries in movement.
Interpretation focuses on identifying potential issues in hip, knee, or ankle mobility, as well as muscle imbalances.
The inline lunge is often employed in fitness and rehabilitation settings to tailor targeted exercises or interventions for improving lower body function and reducing the risk of injury.
|
8 weeks
|
|
active hip flexion test
Time Frame: 8 weeks
|
The Active Hip Flexion Test is a functional movement assessment that evaluates the flexibility and mobility of the hip flexors.
In this test, an individual lies on their back and actively lifts one leg straight up towards their chest while keeping the opposite leg flat on the surface.
The angle of hip flexion is measured, and any limitations or discomfort are noted.
Scoring involves assessing the range of motion, and interpretation focuses on identifying potential hip flexor tightness or restrictions.
This test is commonly used in fitness, sports, and rehabilitation settings to inform targeted exercises or interventions aimed at improving hip flexor flexibility and function.
|
8 weeks
|
|
straight leg raise test
Time Frame: 8 weeks
|
The Straight Leg Raise (SLR) Test is a clinical assessment used to evaluate the flexibility and tension of the hamstrings and the sciatic nerve.
In this test, an individual lies on their back, and one leg is lifted upward while keeping the knee straight.
The angle at which the leg can be raised before experiencing discomfort or tension is measured.
Scoring involves noting the range of motion, and interpretation focuses on identifying potential issues such as hamstring tightness or sciatic nerve irritation.
|
8 weeks
|
|
Push-up
Time Frame: 8 weeks
|
The push-up test is a fitness assessment that measures upper body strength and endurance.
During the test, individuals perform as many push-ups as possible while maintaining proper form, including a straight body alignment.
The number of completed push-ups is recorded, and interpretation varies based on age, gender, and fitness level norms.
|
8 weeks
|
|
Diagonal lift
Time Frame: 8 weeks
|
The Diagonal Lift Test is a functional movement assessment that evaluates the coordination and stability of the core and lower body.
In this test, an individual stands on one leg and lifts the opposite leg diagonally across the body.
The goal is to perform the movement smoothly and with control.
Scoring involves observing balance, fluidity, and any compensations or asymmetries.
Interpretation focuses on identifying potential weaknesses, imbalances, or mobility restrictions in the core and lower extremities.
|
8 weeks
|
|
Seated rotation test
Time Frame: 8 weeks
|
functional movement to help identify compensatory movement pattern and limitation
|
8 weeks
|
|
functional shoulder mobility
Time Frame: 8 weeks
|
The Functional Shoulder Mobility Test is an assessment that evaluates the range of motion and flexibility in the shoulders, emphasizing their functional capacity.
During the test, individuals perform various shoulder movements, such as reaching overhead, across the body, and behind the back.
Scoring involves observing the range of motion, symmetry, and any discomfort or restrictions in the movements.
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Aqsa safdar, DPT, Riphah International University Islamabad
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)
August 1, 2023
Primary Completion (Estimated)
May 1, 2024
Study Completion (Estimated)
May 1, 2024
Study Registration Dates
First Submitted
November 25, 2023
First Submitted That Met QC Criteria
January 18, 2024
First Posted (Estimated)
January 19, 2024
Study Record Updates
Last Update Posted (Estimated)
January 19, 2024
Last Update Submitted That Met QC Criteria
January 18, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 014241 aqsa safdar
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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