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Clinical Trials/NCT06828081
NCT06828081
Active, not recruiting
Not Applicable

Comparative Effects of Getting it Right AddressingShoulderPain(GRASP)Trial and Rotator Cuff Strengthening Exercise Program Among Military Sports for Rotator Cuff Tendinopathy

Riphah International University1 site in 1 country30 target enrollmentStarted: April 24, 2024Last updated:

Overview

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
30
Locations
1
Primary Endpoint
Western Ontario Rotator Cuff Index (WORC)

Overview

Brief Summary

This research will use a randomized clinical trial (RCT) method to get military athletes with rotator cuff tendinopathy. People will be chosen at random to either get the GRASP method or normal exercises for making the shoulder muscles stronger. The main things the investigator will look at are how bad the pain is how well the shoulder works and if they can go back to work or sports. Tests will be done at the start, right after a treatment, and later times to measure the short-term and long-term advantages of the treatments. This study's careful way of doing things aims to provide strong information for military sports medicine. It helps doctors in treating shoulder problems like rotator cuff tendinopathy.

Detailed Description

The rationale for conducting this study lies in the critical need to address rotator cuff tendinopathy, a prevalent and debilitating issue among military athletes. The unique demands placed on military personnel, involving repetitive overhead tasks and rigorous training, contribute significantly to the higher incidence of rotator cuff problems. The impact of this condition on performance, readiness, and overall well-being in the military cannot be overstated.

In the end, the plan for this study wants to fix a gap in what we know right now about dealing with muscle problems in military sports players' shoulders. This study looks at the GRASP trial methods and compares them with standard rotator cuff exercises. It aims to improve treatments and help military staff be healthier and work better.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • People in the military who are between 18 and 50 years old.
  • Active participation in sports activities for the military.
  • Diagnosing rotator cuff tendon pain in medical practice.
  • Basic shoulder movement within a certain range of motion.

Exclusion Criteria

  • History of shoulder surgery.
  • Systemic inflammatory diseases.
  • Disorders of the brain or mind that affect physical actions.
  • Not being able to stick to the plan for later.

Outcomes

Primary Outcomes

Western Ontario Rotator Cuff Index (WORC)

Time Frame: 5-6weeks

The Western Ontario Rotator Cuff Index (WORC) is a self-reported questionnaire that evaluates the quality of life in individuals with rotator cuff disorders across five domains: physical signs and symptoms, sports, work, manner of living, and feelings. It ranges from 0 to 2100, and the lower the total, the better the result.

Inclinometer

Time Frame: 5-6weeks

The inclinometer calculates shoulder R.O.M. in degrees with high accuracy. These are flexion: 170-180° rotation, abduction: 170-180°, external rotation: 90°, and internal rotation: 70-90°.

Push-Up Plus Test

Time Frame: 5-6weeks

The Push-Up Plus Test is designed to assess both scapular stability and serratus anterior muscle strength from the observed scapular movements during the 'plus' action in a push-up formation. They are either pass/fail scores or quantitative repet

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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