Comparative Effects of Pendulum Exercise and Serratus Punch Exercises on Rotator Cuff Pain in Badminton Players

January 10, 2025 updated by: Riphah International University

Comparative Effects of Pendulum Exercise and Serratus Punch Exercises on Rotator Cuff Pain and Disability in Badminton Players

This study will compare the effects of two exercise interventions, pendulum exercises and serratus punches, on rotator cuff pain and injury in badminton players. Using a randomized clinical trial with participants from local clubs, the research will evaluate pain levels, range of motion, and shoulder function after a set period of regular, supervised exercises. The results aim to provide evidence-based insights for effective rehabilitation programs tailored to badminton athletes, supporting better recovery and injury prevention.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Detailed Description

Rotator cuff pain and disability is typical among badminton players because of the dull movements associated with the game. These wounds can prompt critical torment and practical limits, influencing the players' exhibition and prosperity. The focal point of this exploration project is to think about the impacts of two different activity mediations, pendulum activities and serratus punch works, on rotator sleeve agony and injury in badminton players. Understanding the similar adequacy of these activities will contribute essential knowledge to improving designated restoration programs for badminton competitors, further developing their recuperation results and forestalling future wounds.

This exploration will utilize a randomized clinical preliminary plan to research the similar impacts of pendulum activities and serratus punch practices on rotator sleeve agony and injury in badminton players. Members will be selected from neighborhood badminton clubs, and consideration measures will include people with an analyzed or self-revealed history of rotator sleeve torment. The chosen members will be arbitrarily allotted to the pendulum or the serratus punch practice bunch. The mediation time frame will traverse a predefined span, during which members will routinely participate in their doled-out practice. Result estimates will incorporate torment levels, scope of movement, and practical appraisals of the rotator sleeve. Factual examinations will be directed to consider the viability of the two activity mediations and their effect on rotator sleeve agony and injury in badminton players. The consequences of this study are to illuminate proof-based restoration systems customized explicitly for the badminton populace, adding to the enhancement of player well-being and execution.

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

  • Pakistan
    • Punjab
      • Lahore, Punjab, Pakistan, 05450
        • Pakistan Sports Board

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Badminton players aged 15 to 30 years.
  • Individuals with self-reported rotator cuff pain or discomfort
  • Clinically diagnosed rotator cuff pain or discomfort.
  • Individuals with Rotator Cuff Injury.

Exclusion Criteria:

  • Previous shoulder surgeries or fractures.
  • Chronic shoulder conditions unrelated to rotator cuff issues.
  • Inability to perform the prescribed exercises due to other musculoskeletal or medical conditions.
  • Patients with shoulder dislocation.
  • Patients with swelling on shoulder.

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
Active Comparator: Pendulum Exercises
Eighteen participants will perform pendulum exercises, which involve gently swinging the arm to relax shoulder muscles and improve mobility. This low-impact exercise is intended to alleviate tension and increase circulation in the rotator cuff, making it ideal for early-stage shoulder rehabilitation.
Other: Pendulum Exercises
In this group, 18 participants will perform pendulum exercises, which involve leaning forward and allowing the affected arm to hang down, swinging it gently in small circular or side-to-side motions. This exercise is designed to enhance shoulder mobility and promote relaxation of the rotator cuff muscles without straining the shoulder joint. The pendulum movement helps improve circulation and relieve tension in the shoulder area, making it a suitable intervention for individuals experiencing rotator cuff pain.
Active Comparator: Serratus Punch Exercises
Eighteen participants will engage in serratus punch exercises, extending the arm in a controlled punching motion to strengthen the serratus anterior muscle. This exercise promotes shoulder stability and supports rotator cuff function, aiming to reduce pain and improve shoulder control.
Other: Serratus Punch Exercises
In this group, 18 participants will engage in serratus punch exercises, focusing on strengthening the serratus anterior muscle. Participants will perform a punching motion by extending the arm forward while maintaining shoulder stability. This exercise activates the shoulder muscles to enhance scapular control, supporting the rotator cuff and improving overall shoulder function. The goal is to build strength in the stabilizing muscles, which can help alleviate pain and enhance mobility in participants suffering from rotator cuff issues.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
DASH Score
Time Frame: 10 MONTHS
The Disabilities of the Arm, Shoulder and Hand (DASH) score is a self-reported questionnaire that measures the disability and symptoms related to upper extremity conditions. It consists of 30 items assessing difficulties in daily activities and the presence of pain. Scores range from 0 to 100, where 0 indicates no disability and 100 indicates maximum disability. The DASH score is useful for evaluating functional status, tracking treatment outcomes, and guiding rehabilitation in patients with arm, shoulder, and hand issues.
10 MONTHS
Oxford Shoulder Score
Time Frame: 10 months
The Oxford Shoulder Score (OSS) is a patient-reported outcome measure that assesses shoulder pain and disability. It includes 12 items focusing on pain levels and functional limitations related to daily activities. Scores range from 0 to 48, with higher scores indicating better shoulder function. The OSS is commonly used in clinical practice and research to evaluate treatment outcomes for shoulder conditions, providing valuable insights into the patient's perspective on their shoulder health
10 months
Range of motion
Time Frame: 10 months
The shoulder's range of motion will be measured using a goniometer to assess specific movements such as flexion, extension, abduction, and internal/external rotation. Assessments will be conducted at baseline and after the intervention to evaluate improvements in mobility, providing objective data on the effectiveness of the exercise interventions for participants with rotator cuff pain.
10 months

Collaborators and Investigators

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

Sponsor

Riphah International University

Investigators

  • Principal Investigator: Wafa Abid, 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)

April 24, 2024

Primary Completion (Estimated)

January 20, 2025

Study Completion (Estimated)

January 30, 2025

Study Registration Dates

First Submitted

November 18, 2024

First Submitted That Met QC Criteria

November 18, 2024

First Posted (Actual)

November 20, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 10, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • REC/RCR&AHS/24/0430

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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