Point Prevalence of Side Strain in Fast Bowlers and Effectiveness of Core Strength Training.

July 18, 2023 updated by: Riphah International University

Point Prevalence of Side Strain in Fast Bowlers and Effectiveness of Core Strength Training

To find out the prevalence of side strain in fast bowlers and determine the effectiveness of core strength training in treating side strain

Study Overview

Detailed Description

A fast bowler needs to have strong core muscles in order to prevent side strain, which can hider the performance. Variation in deliveries , bowling speed and bowling action can be compromised due to side strain injuries specifically in fast bowlers.

A strong and stable core helps to maintain balance and provide strength while performing repetitive movements such as bowling. Core strengthening program should include exercises that are sports specific, conditioning exercises that focus on anterior and posterior musculature of the trunk and hip.

The aim of this study is to find out the prevalence of side strain in fast bowlers and to incorporate strengthening exercises for core muscles to evaluate its effectiveness for side strain.

Study Type

Interventional

Enrollment (Actual)

36

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

    • Punjab
      • Gujar Khan, Punjab, Pakistan, 47850
        • Sawar Muhammad Hussain Shaheed Sports Stadium, Gujar Khan

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

14 years to 40 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male fast bowlers
  • Age 14 to 40 years

Exclusion Criteria:

  • Athletes who have undergone any surgery
  • Anyone with history of chest pain due to cardiopulmonary disorders

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Core Strength Training Group
The participants of core strength training group will perform core strength training for 6 weeks (3 days per week).

The participants of experimental group will perform core strength training regime for 6 weeks (3 days per week). Each exercise session will last for a period of 45 mins, the exercises would be performed in 3 sets of 5 repetitions with 5 seconds hold time and 10 seconds rest between each repetition and a minutes rest in between each set.

Following exercises would be performed :

Bridge, Crunch, Plank, Side Plank, Mountain Climb.

Active Comparator: Conventional Training Group
The participants of conventional training group will perform conventional exercises for 6 weeks (3 days per week).

The participants of conventional group will perform following exercises :

Running (10 repetitions X 3 sets), Jogging (10 repetitions X 3 sets), Stretching (10 repetitions X 3 sets)

Rest between Exercises : 10-15 Seconds Rest between Set of Exercises : 30-60 Seconds Cricketers will receive exercises for 8 weeks. There will be 3 sessions per week.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Core Muscle Strength Test
Time Frame: 6 weeks

The objective of this evaluation is to monitor the development and improvement of an athlete's core strength and endurance over time.

We will start in the plank exercise position. This is parallel to the ground with your torso straight and rigid, resting your weight on your toes and forearms.

Start in the modified press up position elbows and feet on the ground, hold this position for 60 seconds, lift your right arm off the ground, hold this position for 15 seconds.

Return your right arm to the ground and lift the left arm off the ground, hold this position for 15 seconds, return your left arm to the ground and lift the right leg off the ground, hold this position for 15 seconds, return your right leg to the ground and lift the left leg off the ground, hold this position for 15 seconds, lift your left leg and right arm off the ground.

6 weeks
Sahrmann Core Stability Test
Time Frame: 6 weeks
The Sahrmann core stability test is a 5-level test used to evaluate the ability of the core muscles to stabilize the spine.
6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ultrasonographical assessment of side strain
Time Frame: 6 weeks

The integration of ultrasound imaging with musculoskeletal modelling has the potential to create new opportunities in the study of human movement science.

Ultrasound will be performed by scanning in a location immediately inferior to the tender rib in the longitudinal and transverse directions for iden-tification of a muscle tear. The fibers of the internal oblique muscle lie deep in relation to the external oblique muscle fibres and run in a direction different from the external oblique muscle fibres by passing in a superior and medial direction. The internal oblique muscle appears as a sheet of linear fibril-lar echotexture. Tears were defined as loss of the normal fibrillar echotexture pattern with a hypoechoic gap at the rib or costal cartilage attachment of the internal oblique muscle.

6 weeks
Cornell Musculoskeletal Discomfort Questionnaire
Time Frame: 6 weeks
The Cornell Musculoskeletal Discomfort Questionnaire (CMDQ) was used to assess discomfort. Professor Alan Hedge and Ergonomics students at the Cornell University developed a well-designed data collection tool named CMDQ. The CMDQ is a 54-item questionnaire that includes a body chart and questions about musculoskeletal ache, pain, or discomfort occurrence in 20 parts of the body over the past week.
6 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Saad Rauf, Ph.D*, Riphah University

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 1, 2022

Primary Completion (Actual)

February 1, 2023

Study Completion (Actual)

July 12, 2023

Study Registration Dates

First Submitted

January 13, 2023

First Submitted That Met QC Criteria

January 23, 2023

First Posted (Actual)

January 25, 2023

Study Record Updates

Last Update Posted (Actual)

July 19, 2023

Last Update Submitted That Met QC Criteria

July 18, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/01402 Siraj ul Haq

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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