Validity and Reliability of the Scapular Muscular Endurance Test

April 14, 2025 updated by: Kubra Koce, Istinye University

Validity and Reliability of the Scapular Muscular Endurance Test in Adolescents

The scapula plays a crucial role in proper shoulder function, contributing to synchronized scapular rotation during humeral motion, serving as a stable base for rotator cuff activation, and acting as a key link in the kinetic chain. Each of these functions is essential for optimal arm movement and depends on the integrity of the surrounding shoulder anatomy. However, bone and soft tissue damage, as well as muscle weakness and shortening, can alter the scapula's roles, affecting both its resting position and dynamic motion. This altered scapular position and/or motion is referred to as scapular dyskinesia.

Although scapular dyskinesia is commonly observed in shoulder injuries, it is generally considered a nonspecific response to shoulder pain rather than a direct consequence of a specific glenohumeral pathology. Therefore, assessing the presence or absence of scapular dyskinesia is a critical component of clinical evaluation. A comprehensive assessment should include a visual examination of the scapula at rest and during dynamic humeral movements, as well as objective measurements of posture and the performance of scapular corrective maneuvers. These evaluations assist clinicians in determining the extent to which scapular involvement contributes to a given shoulder injury.

The treatment of scapular dyskinesia should begin with optimizing anatomical alignment, followed by restoring dynamic scapular stability through the strengthening of scapular stabilizers using kinetic chain-based rehabilitation protocols. The kinetic chain, as defined by Steindler, is "a combination of successive joints containing complex motor units." It describes the interconnected movement of joints, where adjacent segments interact to form a continuous chain of motion. This biomechanical model emphasizes that dysfunction in any part of the chain can impact movement quality in both upper and lower segments. The scapula is a foundational component within this system, with surrounding muscles playing a crucial role in stabilizing it.

Postural disorders such as kyphosis can lead to scapular deformities, negatively affecting scapular stability. Rehabilitation professionals and researchers increasingly use the Scapular Muscular Endurance Test (SMET) to assess scapular stability. Given that adolescents are at a heightened risk for musculoskeletal injuries, upper extremity assessments like the SKET may contribute significantly to evaluating this population. However, the validity and reliability of the SMET in adolescents have yet to be established.

This study aims to determine the validity and reliability of the SKET in adolescents.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

67

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

      • Istanbul, Turkey, 34010
        • Istinye University

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

N/A

Sampling Method

Probability Sample

Study Population

Adolescents between the ages of 10-19 will be included.

Description

Inclusion Criteria:

  • Being between 10-19 years old
  • Being willing to participate in the study

Exclusion Criteria:

  • Those who have had major surgery or trauma related to the musculoskeletal system, especially the upper extremity and scapular region
  • Those with neurological diseases
  • Those with rheumatic diseases in the active phase
  • Those with systemic diseases (Diabetes, hypothyroidism, infection, malignancy...)

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Group 1
Adolescents
The group in which the assessments will be made.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Scapular Endurance Test
Time Frame: 2 weeks
The endurance of the scapular muscles will be evaluated with the Scapular Muscular Endurance Test (SMET). The SMET will be performed with the participants standing facing the wall, with the shoulders and elbows in a 90° flexion position. When both scapulae are in a neutral position, the most suitable length of 10 wooden bars of different lengths (18-36 cm) will be placed between the participant's elbows and a dynamometer will be placed between the participant's hands. In this position, the participant will be asked to perform shoulder external rotation until a load of one kilogram is reached on the dynamometer and to maintain this force, and the results will be recorded in seconds. The time the participant meets the test conditions will be recorded in seconds with a stopwatch. The test will be repeated twice with a five-minute break for rest, with the best score recorded for analysis.
2 weeks
Closed Kinetic Chain Upper Extremity Stability Test
Time Frame: 2 weeks
It will be used to evaluate upper extremity strength, endurance, and closed kinetic chain. The test will be performed following the instructions defined by de Oliveira et al. During the test, male participants will be placed in a push-up position and female participants in a modified push-up position (with knee support) on 2 tapes attached to the floor with a distance of 90 cm between their hands. Participants will be asked to touch their other hand with one hand while maintaining the push-up position for 15 seconds and the number of repetitions completed for the right and left will be recorded. The test will be repeated three times and the average of the values will be recorded. 45-second rest breaks will be given between each test.
2 weeks

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)

February 25, 2025

Primary Completion (Actual)

March 30, 2025

Study Completion (Actual)

April 14, 2025

Study Registration Dates

First Submitted

February 24, 2025

First Submitted That Met QC Criteria

February 24, 2025

First Posted (Actual)

February 26, 2025

Study Record Updates

Last Update Posted (Actual)

April 15, 2025

Last Update Submitted That Met QC Criteria

April 14, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 24-30

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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