Effects of Isolated and Integrated Core Stability Training in Fast Bowlers

January 18, 2025 updated by: Sehat Medical Complex

Effects of Isolated and Integrated Core Stability Training on Power, Balance and Performance in Fast Bowlers

The objective of this study will be to compare the effects of isolated and integrated core stability training on power, balance and performance in fast bowlers.

Study Overview

Detailed Description

Athletes consistently strive for improved performance, often incorporating strength and conditioning routines that inevitably include elements of core strengthening. The crucial question emerges: how does enhancing core strength and stability contribute to elevated athletic performance? Before delving into this issue, it is essential to clarify the concept of core strength and stability. The core consists of both passive and active components, including bones, muscles, and ligaments in the lumbar spine, pelvis, and hips. Core strength is characterized by the capacity of the core muscles to produce and sustain force. In contrast, core stability emphasizes the significance of passive and active stabilizing elements within the lumbo-pelvic area. Beyond mere strength, core stability denotes the adeptness of these stabilizers to uphold proper trunk and hip posture, equilibrium, and control during both stationary and kinetic activities. It can be conceptualized as the ability to sustain command over the core while exerting core strength or when met with external disruptions.

The objective of this study will be to compare the effects of isolated and integrated core stability training on power, balance and performance in fast bowlers. This study will be a Randomized Clinical trial. Data will be collected fromPakistan Sports Board, Lahore. Subjects fulfilling the inclusion criteria will be included in this study. Baseline measurements will be taken before the application of interventions. Treatment will be then given to control and intervention group according to their allocation. Post-Treatment values for the baseline measures will be taken. Pre, 6th week and 12th week post treatment values will be analyzed. All subjects received a total of three treatment sessions in a week over the period of 12 weeks. The data will be analyzed using SPSS v 25.

Study Type

Interventional

Enrollment (Estimated)

28

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 Contact Backup

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan, 54000
        • Recruiting
        • Riphah International University
        • Contact:
        • Contact:
        • Contact:
          • Laiba Sarwar Dr., DPT, MS-SPT

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:

  • • Age group: 18 to 28 years. Individuals younger than 18 needed parental consent, and those older than 30 faced a higher likelihood of degeneration in the thoracic and lumbar spine region

    • No history of lower back pain
    • Gender: Male. Considering the differences in anatomy and physiology between males and females, it was deemed advantageous to concentrate solely on one gender to ensure continued homogeneity
    • They had actively participated in Action Cricket within one of the intermediate leagues for a minimum of six months

Exclusion Criteria:

  • Athletes with physical disability and major health problems.
  • Not willing to participate.
  • Patients with MSK disorders.
  • Female athletes will not be included because of anatomical and physiological differences.
  • Participants with a recent history of significant injuries, especially those related to the core or lower extremities, as this could confound the study results.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Isolated Core Stability Program
The control group consists of basic core exercises which include the activation of transversusabdominins and multifidus muscles and progressive strengethening of these muscles in all positions using swiss balls and floor mats. All exercises were done for at least 3 sets of 15 repetitions to build proper core stability.
The control group consists of basic core exercises which include the activation of transversusabdominins and multifidus muscles and progressive strengethening of these muscles in all positions using swiss balls and floor mats. All exercises were done for at least 3 sets of 15 repetitions to build proper core stability.
Experimental: Integrated Core Stability Program

An individualized protocol was designed for these cricketers targeting static and dynamic core stability, with integration of balance, endurance and power component.

Tranversusabdominis and multifidus strengthening is combined with upper extremity motions to work on the fast bowling action i.e throwing of the players.

At the same time lower extremity balance and strengthening is also included to ensure the high speed of sprint.

An individualized protocol was designed for these cricketers targeting static and dynamic core stability, with integration of balance, endurance and power component.

Tranversusabdominis and multifidus strengthening is combined with upper extremity motions to work on the fast bowling action i.e throwing of the players.

At the same time lower extremity balance and strengthening is also included to ensure the high speed of sprint.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Seated Medicine Ball Throw Test (SMBT):
Time Frame: 12 weeks
The seated medicine ball throw (SMBT) serves as a field test designed to evaluate upper-body muscular power by gauging the maximum distance an individual can propel a medicine ball from a seated position. This assessment is cost-effective and easier to integrate into a field test battery compared to alternative methods for evaluating upper body power. Demonstrating validity and reliability, participants engage in the SMBT by throwing a 2 kg medicine ball with a 19.5 cm diameter while positioned on the floor, with the upper torso against the wall and legs extended, maintaining a trunk angle of 90°.
12 weeks
Sit Up Test (SUT)
Time Frame: 12 weeks
The participant assumes a supine position on the floor, with knees flexed at a 90° angle, hands positioned beside their head, and elbows directed straight forward. A proper execution of the sit-up involved touching the elbows to the knees and then returning to the starting position, ensuring that the shoulders made contact with the floor. The number of repetitions completed was documented to quantify the level of endurance achieved in each trial. Exhaustion, defined as the inability to execute another repetition, marked the conclusion of the test. The Sit-Up Test (SUT), characterized by its simplicity of administration and low costs, proved to be an effective tool for assessing muscle endurance
12 weeks
Star Excursion Balance Test (SEBT):
Time Frame: 12 weeks
The SEBT was initially outlined with the individual positioned at the center of eight lines forming an eight-pointed star, each with a 45° separation. Subsequent studies demonstrated that this approach could be streamlined with just three lines, referred to as anterior (ANT), posteromedial (PM), and posterolateral (PL), based on the stance foot. This simplified version, commonly known in the literature as the mSEBT, is now frequently employed, though not consistently. The adoption of the mSEBT helps save testing time by eliminating redundant testing directions while upholding the consistency and reliability observed in the original SEBT. Typically, the average of the three directions is calculated to generate a composite score (COMP)
12 weeks

Collaborators and Investigators

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

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.

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)

November 30, 2024

Primary Completion (Estimated)

May 25, 2025

Study Completion (Estimated)

May 30, 2025

Study Registration Dates

First Submitted

October 17, 2024

First Submitted That Met QC Criteria

November 13, 2024

First Posted (Actual)

November 14, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 18, 2025

Last Verified

November 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR&AHS/24/0425

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

product manufactured in and exported from the U.S.

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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