- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05646914
Plyometric and Complex Training in Male Cricket Players
December 5, 2022 updated by: Masood Khan, King Saud University
Effect of Plyometric and Complex Training on Physical Performance in Male Cricket Players: a Randomized Controlled Trial
The complex training starts with a high load of resistance training that is succeeded by plyometric training.
This combination aims at improving the efficacy of the plyometric training stimulus, thus increasing the neuromuscular response, explosive strength, and power.
This response might further be improved by making appropriate variations in the dosage parameters of complex training.
Previously available literature reports conflicting evidence, with some studies supporting the effectiveness of complex training for improving power output in sports, whereas others contradict this rationale.
There is a paucity of research evidence that directly compares the efficacy of plyometric and complex training for the outcomes of physical performance in cricket players.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
42
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
-
-
-
Riyadh, Saudi Arabia, 11433
- King Saud University
-
-
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
18 years to 26 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- University-level cricket players
- Age of 18 to 26 years
- Playing competitively at least once a month
- Involved in resistance training for at least six months
- Working knowledge of the english language
Exclusion Criteria:
- A history of severe neurological deficit, injury or concussion in the past six months,
- Operative treatment for lower or upper limb in the past six months,
- Current musculoskeletal pain (any level of chronicity)
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Complex training group
Plyometric exercises along with resistance exercises were performed.
|
Squats and drop jumps, Barbell step-ups and hops, Bench press and plyometric press-up, Barbell lunge and box jumps were performed.
|
|
Active Comparator: Plyometric training group
Plyometric exercises were performed.
|
Drop Jumps, Hops, Plyometric press-up, Box Jumps were performed.
|
|
No Intervention: Control group
Routine training was performed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Core Muscle Strength
Time Frame: 4 weeks.
|
Athletes assumed a pike position with the elbows under the shoulders, the forearms shoulder-width apart on the floor, toes on the floor, buttocks in a neutral position, and the body in a straight line.
|
4 weeks.
|
|
Multistage Fitness
Time Frame: 4 weeks.
|
For this test, the subject had to run between two lines marked 66 feet apart (20 meters).
Pre-recorded beeps were played, and the subjects had to increase their speed with each beep, thereby determining their aerobic fitness based on the number of laps completed.
|
4 weeks.
|
|
Push-Up
Time Frame: 4 weeks.
|
The subjects performed the push-up with their hands and toes touching the floor.
In the eccentric phase, the subjects moved down until they were at a 5 cm distance from the floor.
The total number of push-ups completed in proper form was counted.
|
4 weeks.
|
|
Lateral Cone Jump
Time Frame: 4 weeks.
|
Two cones were kept with a crossbar or tape fastened across them with the subject standing on one side.
The subjects were made to jump to cross the bar and land on the opposite side.
The time was started as soon as the subject's foot left the ground, and the total number of lateral jumps performed in 30 seconds was counted.
|
4 weeks.
|
|
Stationary Vertical Jump
Time Frame: 4 weeks.
|
A tape measure was attached to the wall, with the subject standing adjacent to it.
They were supposed to touch the highest point on the wall with their inked middle fingertip.
This point was taken as the standing height of the subject.
Then, the subject performed a vertical jump with the assistance of both arms and legs to reach the maximum possible height and marked the wall with their inked middle fingertip.
The difference between the two points was calculated as the final score.
|
4 weeks.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
December 15, 2015
Primary Completion (Actual)
May 23, 2016
Study Completion (Actual)
June 16, 2016
Study Registration Dates
First Submitted
December 5, 2022
First Submitted That Met QC Criteria
December 5, 2022
First Posted (Estimate)
December 12, 2022
Study Record Updates
Last Update Posted (Estimate)
December 12, 2022
Last Update Submitted That Met QC Criteria
December 5, 2022
Last Verified
December 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 16.11.2015
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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