Shoulder Pain and Scapular Endurance (SME)

March 25, 2023 updated by: Erhan KIZMAZ, Pamukkale University

The Effect of Regular Exercising on Shoulder Pain and Scapular Endurance

Objective: This study aimed to investigate the effects of regular exercising on scapular muscle endurance and shoulder pain in young individuals.

Methods: Participants' clinical and sociodemographic properties recorded, scapular muscle endurance assessed with Scapular Muscular Endurance (SME) test, and shoulder pain severity questioned using the Visual Analogue Scale.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Background: Serratus Anterior and Trapezius muscles are the most important stabilizers of the scapulothoracic joint. The inadequate endurance of these muscles plays an important role in the decreased neuromuscular performance.

Objective: This study aimed to investigate the effects of regular exercising on scapular muscle endurance and shoulder pain in young individuals.

Methods: Participants' clinical and sociodemographic properties recorded, scapular muscle endurance assessed with Scapular Muscular Endurance (SME) test, and shoulder pain severity questioned using the Visual Analogue Scale.

Study Type

Interventional

Enrollment (Actual)

200

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

    • Pamukkale
      • Denizli, Pamukkale, Turkey, 20100
        • Aziz Dengiz

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

17 years to 25 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

for exercise group;

  • between 17-25 years ages
  • who were using the fitness center by their preference (not professional)
  • had active sporting life (not professional)
  • who were regularly exercising

for sedentary group;

  • between 17-25 years ages
  • who had sedentary life style

Exclusion Criteria:

for boths group;

  • Individuals who had surgical stabilization,
  • who had previous shoulder complex fractures
  • who had positive impingement test results
  • who had systemic diseases
  • who had neurological and orthopedic problems

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: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: The Scapular Muscles Endurance (SME
The Scapular Muscles Endurance (SME) test was used to assess the endurance of the Serratus Anterior muscles.
EXERCISE FOR HEALTH AND PAIN IMPROVEMENT
Other: Vizual Analog Scale
The VAS for pain, measures pain severity in the affected shoulder from 0 to 10 points, with 0 points representing no pain at all and 10 points representing pain as bad as it can be
EXERCISE FOR HEALTH AND PAIN IMPROVEMENT

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Scapular Muscles Endurance (SME) test
Time Frame: Evaluation was done at the first meeting with the participants.
The Scapular Muscles Endurance (SME) test was used to assess the endurance of the Serratus Anterior muscles. For this test, the participant stood against the wall with their shoulders and elbows flexed to 900. There was no contact between the participant's arms and the wall. The subjects then held a green elastic exercise band (with a resistance of 2.3 kg, when stretched 100%), and an adjustable ruler was placed between their elbows to maintain the test position. While both scapulae were neutrally positioned, the participant was then asked to externally rotate the shoulders and to maintain this force for as long as they could hold and the holding duration was recorded in second. The test was ended when the participant was unable to maintain the resistance and dropped the adjustable ruler, failed to maintain 900 of shoulder flexion, or reported an unacceptable increase in discomfort (Edmondston et al. 2008).
Evaluation was done at the first meeting with the participants.
Vizual Analog Scale
Time Frame: Evaluation was done at the first meeting with the participants.
measures pain severity in the affected shoulder from 0 to 10 points, with 0 points representing no pain at all and 10 points representing pain as bad as it can be
Evaluation was done at the first meeting with the participants.

Collaborators and Investigators

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

Investigators

  • Study Director: Nilüfer çetişli korkmaz, Prof. Dr., Pamukkale University
  • Study Chair: Esra Doğru HUZMELİ, Assoc Prof, Mustafa kemalU

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 15, 2018

Primary Completion (Actual)

July 20, 2021

Study Completion (Actual)

January 15, 2022

Study Registration Dates

First Submitted

March 14, 2023

First Submitted That Met QC Criteria

March 25, 2023

First Posted (Actual)

March 28, 2023

Study Record Updates

Last Update Posted (Actual)

March 28, 2023

Last Update Submitted That Met QC Criteria

March 25, 2023

Last Verified

March 1, 2023

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

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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