- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05317949
Effect of Integrated Neuromuscular Training on Medium Fast Bowler in Cricket
Effect of Integrated Neuromuscular Training on Explosive Strength, Speed and Endurance of Medium Fast Bowler in Cricket
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Integrated neuromuscular training (INT) is a combination of functional movement training and specific strength, balance, speed, sensitivity, and isometric training, which aims to evaluate and prevent sports injury and improve sports performance. Neuromuscular control defects are mainly manifested as decreases in muscle strength, explosive power, or abnormal activation patterns. INT is defined as a conceptual training program that incorporates general (e.g., fundamental movements) and specific strength and conditioning tasks (e.g., resistance, balance, agility, plyometric) to improve injury resilience and to enhance sporting and motor skill performance. The majority of studies in youth examining neuromuscular training strategies to improve performance and injury prevention include multiple components (for example, balance, strength, plyometric, agility, speed, coordination. INT sessions are characterized by short bursts of physical activity interspersed with brief rest periods.
the purpose of this study is to find the effect of integrated neuromuscular training on explosive strength, speed and endurance of medium fast bowler in cricket
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
KPK
-
Peshawar, KPK, Pakistan, 24840
- Sports Complex
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Medium fast bowlers
- Players playing cricket for > 1 year
- Players engaging in cricket ≥ 3 days in a week
Exclusion Criteria:
- History of any injury in past 6 months.
- Those players having musculoskeletal, neurological, cardiorespiratory problems
- Those players who have any medical condition
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Integrated neuromuscular training program group
Integrated neuromuscular training program group will perform exercise in three major domains
|
Integrated neuromuscular training program group will do plyometric training, speed and sensitivity training, resistance training for 3 days in a week and total for eight weeks.
|
|
Active Comparator: General fitness exercises program group
General fitness exercises program group will perform general fitness exercises
|
General fitness exercises program group will do general fitness exercise for 3 days in a week and total for eight weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Soft Ball Throw Test
Time Frame: Eight weeks
|
the test involves throwing a soft for maximum distance this test measure explosive power, particularly of the upper body and evaluate throwing distance
|
Eight weeks
|
|
50 Yard Dash
Time Frame: Eight weeks
|
The aim of this test is to determine acceleration and speed procedure : The test involves running a single maximum sprint over 50 meters, with the time recorded.
|
Eight weeks
|
|
1 Mile Run Test
Time Frame: Eight weeks
|
The purpose of this test is to complete one mile in the fastest possible time.
After the purpose of the test and instructions are given, the participants begin running on the count "Ready?
Go!"
|
Eight weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Aadil Omer, Ph.D*, 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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- REC/01254 Nadeem Afsar
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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