Efficacy of Adding Early Scapular Muscles Strengthening Exercise After Rotator Cuff Repair on Scapula Kinematics

March 18, 2026 updated by: Ramy Zohdy Hassan Ahmed, Cairo University

Early Strengthening of Lower Trapezius and Serratus Anterior Muscles in an Accelerated Rehabilitation Program After Rotator Cuff Repair

The study investigates the effect of accelerate rehabilitation protocol(adding scapular strengthen exercises (lower trapezius and serratus anterior) from week 1) after arthroscopic rotator cuff repair on scapular upward rotation during shoulder elevation.

Study Overview

Detailed Description

The study will consist of two groups, each participating in an accelerated rehabilitation program that will start in the first week after surgery and continue until week 12. However, the groups will follow different protocols.

The first group will follow an accelerated rehabilitation protocol with early strengthening of the scapular stabilizer muscles, specifically the lower trapezius (LT) and serratus anterior (SA). This group will begin gradual active range of motion (ROM) for the glenohumeral (GH) joint from week 4 post-operative until week 12, as well as scapular muscle strengthening exercises starting from the first week.

The second group will follow a protocol with delayed strengthening of the scapular stabilizer muscles. In this group, active ROM for the GH joint and scapular activation exercises (including protraction, retraction, and depression) will begin from week 6 and continue until week 12.

Patients will be required to wear a sling for the first 6 weeks or as recommended by the physician, removing it only during therapy sessions and home exercises.

Outcomes will be measured at three points: at week 3 for baseline assessment, and then reassessed at weeks 6 and 12.

Study Type

Interventional

Enrollment (Actual)

30

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

      • Alexandria, Egypt, 03
        • wengat hospital (El Raml Children hospital)
      • Alexandria, Egypt
        • wengat hospital (El Raml Children hospital)

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

No

Description

Inclusion Criteria:

  1. Patients after arthroscopic rotator cuff repair.
  2. Both gender between age 30 to 50 years
  3. Small and medium supraspinatus tear

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: Early strengthening of Scapular stabilizer muscle and GH Active range of motion
Act as study group will receive accelerated protocol with early strengthening of scapular stabilizer muscle of lower trapezius, and serratus anterior and early active GH range of motion (AESA) rehabilitation program.
adding early scapular strengthening (lower trapezius and serratus anterior) exercise in Rehabilition program after rotator cuff repair surgery
Active Comparator: Delay strengthening of Scapular stabilizer muscles and GH Active range of motion
Act as control group will receive Accelerated protocol with delay strengthening of scapular stabilizer muscles and GH active range of motion (ADSA) rehabilitation program
adding early scapular strengthening (lower trapezius and serratus anterior) exercise in Rehabilition program after rotator cuff repair surgery

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Upward rotation of the scapula
Time Frame: At week 3 and week 9 and week 12 after arthroscopic rotator cuff repair
Measuring the degree of upward rotation of the scapula during shoulder elevation using baseline bubble inclinometer
At week 3 and week 9 and week 12 after arthroscopic rotator cuff repair

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
glenohumeral shoulder elevation
Time Frame: At week 3 and week 9 and week 12 after arthroscopic rotator cuff repair
Measuring the degree of glenohumeral shoulder flexion, abduction, internal rotion and external rotation using a baseline bubble inclinometer
At week 3 and week 9 and week 12 after arthroscopic rotator cuff repair
scapular muscles strength
Time Frame: At week 3, week 9 and week 12 after arthroscopic rotator cuff repair
measuring the muscle strength for the serratus anterior, lower trapezius, and upper trapezius using the Active Force 2 device dynamometer
At week 3, week 9 and week 12 after arthroscopic rotator cuff repair

Collaborators and Investigators

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

May 1, 2024

Primary Completion (Actual)

March 1, 2025

Study Completion (Actual)

May 1, 2025

Study Registration Dates

First Submitted

February 17, 2025

First Submitted That Met QC Criteria

February 26, 2025

First Posted (Actual)

February 28, 2025

Study Record Updates

Last Update Posted (Actual)

March 20, 2026

Last Update Submitted That Met QC Criteria

March 18, 2026

Last Verified

September 1, 2024

More Information

Terms related to this study

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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