- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05788380
Shoulder Pain and Scapular Endurance (SME)
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
Conditions
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pamukkale
-
Denizli, Pamukkale, Turkey, 20100
- Aziz Dengiz
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Investigators
- Study Director: Nilüfer çetişli korkmaz, Prof. Dr., Pamukkale University
- Study Chair: Esra Doğru HUZMELİ, Assoc Prof, Mustafa kemalU
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MUŞALPARSLAN
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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