Effects of Complex Training in Cricket Fast Bowlers

March 4, 2024 updated by: Riphah International University

Effects of Complex Training on Physical Fitness, Bowling Performance, Work Capacity, Muscle Strength and Bone Density in Cricket Fast Bowlers

This study will be a randomized controlled trial and the data will be collected from National Cricket Academy and domestic cricket clubs. The sample size will be calculated by conducting a pilot study. There will be three groups. Group-A will be receiving Complex training, Group-B will be receiving Conventional training and Group C as a Control Group. Athletes with same physical fitness level will be recruited. There will be parallel assignment of the participants. Assessor will be kept blinded. All the parameters would be assessed at Baseline, 6 Weeks, 12 Weeks. Physical fitness will be assessed through Field Testing. Bowling performance will be assessed through speed machine and Kinovea Software. Work capacity will be assessed through step testing. Muscle strength will be assessed through Dynamometer. Lastly, BMD will be assessed though Bone Densitometer.

Study Overview

Detailed Description

Cricket fast bowlers require a unique blend of speed, strength, power, and agility to excel in their role on the field. In recent years, Complex training has emerged as a popular training method to enhance these critical qualities among fast bowlers. Complex training involves combining strength exercises with explosive, sport-specific movements in a single training session, aiming to improve overall athletic performance. This study will be a randomized controlled trial and the data will be collected from National Cricket Academy and domestic cricket clubs. The sample size will be calculated by conducting a pilot study. There will be three groups. Group-A will be receiving Complex training, Group-B will be receiving Conventional training and Group C as a Control Group. Athletes with same physical fitness level will be recruited. There will be parallel assignment of the participants. Assessor will be kept blinded. All the parameters would be assessed at Baseline, 6 Weeks, 12 Weeks. Physical fitness will be assessed through Field Testing. Bowling performance will be assessed through speed machine and Kinovea Software. Work capacity will be assessed through step testing. Muscle strength will be assessed through Dynamometer. Lastly, BMD will be assessed though Bone Densitometer.

Study Type

Interventional

Enrollment (Estimated)

40

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

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan, 54000
        • Recruiting
        • Pakistan Sports Board Coaching Center
        • Contact:
          • Nasrullah Rana
          • Phone Number: +92 334 5492964
        • Principal Investigator:
          • Muhammad Atif Javed, PP-DPT
        • Sub-Investigator:
          • Syed Asadullah Arslan, Ph.D.

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:

  • Male bowlers between 18 - 25 years
  • Bowling speed 115-130 km/h
  • Same Run-up speed (20-25 km/h)
  • domestic teams
  • Active in game from last 6 months
  • Athletes with same 1 Repetition Maximum (Bench press and Leg press)
  • Athletes with same BMI category (18.5 - 24.9)

Exclusion Criteria:

  • Red flags
  • Resistance training from last 6 months
  • Any disabling musculoskeletal injury
  • Glenohumeral Internal Rotation Deficit
  • Scapular Dyskinesia
  • Athletes taking prohibited drugs, Ergogenic aids
  • Any cardiovascular issue . Any systemic disease

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
Other: Control Group
No intervention given
Active Comparator: Conventional Training

Week 0-4 Session 1 Rotator cuff wall compression Forearm flexor compression Alpha ball tricep scrape Band assisted pushups Session 2 Soft ball thoracic breathing Neck ball arm rotations ITb compressions Middle quard compressions

Week 4-8 Session 1 Kneeling pall of band hold Kneeling pall of partner proturbations Leg lower with mediball neutral Half lying arm speed and swing drill Session 2 Single leg band hold Trunk activated psoas lowers Split clam Bulgarian split iso hold

Week 8-12 Session 1 Point kneel thoracic rotations Side lying single arm thoracic abduction Banded side lying clams Side lying abduction from glute Session 2 Low back mobility Kneeling pall off band hold Clean and jerks power drill movements Weighted bench press Session 3 Standing band rotations thoracic only Band pull aparts Tennis ball in trap arm flexion ext thumb to floor Bulgarian weighted

Experimental: Complex Training

Week 1-4: Foundation Phase Lower Body Resistance Training Squats (Back Squats or Goblet Squats) Deadlifts Lunges

Paired with:

Box Jumps Depth Jumps

Upper Body Resistance Training Bench Press Overhead Press

Paired with:

Medicine Ball Chest Pass Medicine Ball Overhead Throw Rows (Barbell or Dumbbell)

Week 5-8: Strength and Power Phase Lower Body Resistance Training Power Cleans Front Squats Romanian Deadlifts

Paired with:

Box Jumps with Barbell Depth Jumps with Medicine Ball

Upper Body Resistance Training Push Press Pull-Ups or Lat Pulldowns Bent Over Rows

Paired with:

Plyometric Push-Ups Medicine Ball Slam

Week 9-12: Power and Speed Phase Lower Body Resistance Training Snatch Split Squats Jumping Lunges

Paired with:

Box Jumps with Barbell Depth Jumps with Medicine Ball

Upper Body Resistance Training Speed Bench Press Face Pulls Plyometric Pull-Ups

Paired with:

Medicine Ball Chest Pass Medicine Ball Overhead Throw

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical fitness (linear speed capability)
Time Frame: 0 week, 6 week, 12 week
will be assessed by lower body vertical jump test
0 week, 6 week, 12 week
Physical fitness (lower limb explosive power)
Time Frame: 0 week, 6 week, 12 week
will be assessed by 20-m sprint test
0 week, 6 week, 12 week
Physical fitness (upper body strength test)
Time Frame: 0 week, 6 week, 12 week
will be assessed by bench press & bent over row
0 week, 6 week, 12 week
Physical fitness (lower body strength test)
Time Frame: 0 week, 6 week, 12 week
will be assessed by hex-bar deadlift
0 week, 6 week, 12 week
Physical fitness (upper body muscular endurance)
Time Frame: 0 week, 6 week, 12 week
will be assessed by horizontal pull
0 week, 6 week, 12 week
Physical fitness (aerobic capacity)
Time Frame: 0 week, 6 week, 12 week
will be assessed by Yo-Yo intermittent recovery Level 1 test
0 week, 6 week, 12 week
Bowling performance (Ball speed)
Time Frame: 0 week, 6 week, 12 week
will be measured by Pocket Radar
0 week, 6 week, 12 week
Bowling performance (run-up time)
Time Frame: 0 week, 6 week, 12 week
will be measured by Dartfish software
0 week, 6 week, 12 week
Bowling performance (accuracy)
Time Frame: 0 week, 6 week, 12 week
will be measured by Dartfish software
0 week, 6 week, 12 week
Bowling performance (RPE)
Time Frame: 0 week, 6 week, 12 week
will be measured by Borg scale
0 week, 6 week, 12 week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Work capacity
Time Frame: 0 week, 6 week, 12 week
will be assessed by Step Testing
0 week, 6 week, 12 week
Muscle Strength
Time Frame: 0 week, 6 week, 12 week
will be assessed by Hand-held Dynamometer
0 week, 6 week, 12 week
Bone Density
Time Frame: 0 week, 6 week, 12 week
will be assessed by Bone Densitometer
0 week, 6 week, 12 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Muhammad Atif Javed, PP-DPT, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

June 16, 2023

Primary Completion (Estimated)

June 1, 2024

Study Completion (Estimated)

June 1, 2024

Study Registration Dates

First Submitted

January 28, 2024

First Submitted That Met QC Criteria

March 4, 2024

First Posted (Actual)

March 5, 2024

Study Record Updates

Last Update Posted (Actual)

March 5, 2024

Last Update Submitted That Met QC Criteria

March 4, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR & AHS/23/1104

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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