- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04296539
Compare the Scapular Muscular Endurance, Stabilization and Dyskinesis Parameters of Sedentary Individuals
July 31, 2023 updated by: Prof. Dr. Sıddıka Fatma Uygur, Cyprus International University
Investigation of the Effect of Regular Exercise on Scapular Muscular Endurance, Scapular Stabilization and Dyskinesia
The aim of this study was to compare the parameters of scapular muscular endurance, scapular stabilization, scapular dyskinesia, upper extremity functional status and postural alignment of adult women aged between 40-65 years old who were performing clinical pilates exercises regularly compared with sedentary adult women in the same age group and to determine whether regular exercise had an effect on these parameters.
Study Overview
Status
Completed
Conditions
Detailed Description
The aim of this study was to compare the parameters of scapular muscular endurance, scapular stabilization, scapular dyskinesia, upper extremity functional status and postural alignment of adult women aged between 40-65 years old who were performing clinical pilates exercises regularly compared with sedentary adult women in the same age group and to determine whether regular exercise had an effect on these parameters.
A total of 70 individuals were included in the study, including 35 individuals performing regular clinical pilates exercises and 35 individuals with sedentary lifestyles.
Clinical pilates group was selected from the individuals who participated in the exercise program under the control of a physiotherapist regularly for 1 hour, 2-3 days a week for at least 6 months.
Socio-demographic characteristics, health status and exercise habits of the participants were recorded.
For scapular muscle strength assessment, digital hand dynamometer; for scapular muscular endurance assessment, Scapular Muscular Endurance Test (SMET) and Shoulder External Rotation Fatigue Protocol; for the assessment of scapular dyskinesia, Lateral Scapular Slide Test (LSST) and Lennie test; for assessment of upper extremity functional status, Disabilities of the Arm, Shoulder and Hand Questionnaire (DASH); for the assessment of postural alignment, the New York Posture Assessment Test were used.
Study Type
Observational
Enrollment (Actual)
70
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
-
-
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Mersin, Turkey, 33000
- Cyprus International University
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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
40 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
70 Women, 35 Sedentary and 35 Doing Regular Clinical Pilates Exercise
Description
Inclusion Criteria:
- Individuals who perform clinical pilates exercises regularly for at least 6 months and at least 2 days a week (pilates group)
- Individuals who are not actively involved in any sports and do not exercise / physical activity regularly (sedentary group)
Exclusion Criteria:
- Individuals diagnosed with scoliosis or any other orthopedic and neurological problems
- Individuals who have had any diagnosis / treatment or had previous surgery due to shoulder and shoulder circumference problems in the last 6 months
- Individuals with shoulder elevations less than 140 degrees
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
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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Sedentary
Involving little exercise or physical activity
|
Exercise
Subjects who were performing regularly pilates exercises for at least six months
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Scapular Dyskinesia
Time Frame: Twenty minutes
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Scapular Malpositioning, Inferior medial border prominence where the scapula is protracted and is in a anteriorly tilted position.
|
Twenty minutes
|
Scapular muscular endurance
Time Frame: Fifteen minutes
|
Repetition and duration of scapular muscles submaximal load
|
Fifteen minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ozge Ozalp, PhD, Cyprus International University
- Study Chair: Baran Yosmaoglu, Professor, Başkent University
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)
March 20, 2019
Primary Completion (Actual)
June 27, 2019
Study Completion (Actual)
June 27, 2019
Study Registration Dates
First Submitted
March 3, 2020
First Submitted That Met QC Criteria
March 4, 2020
First Posted (Actual)
March 5, 2020
Study Record Updates
Last Update Posted (Actual)
August 2, 2023
Last Update Submitted That Met QC Criteria
July 31, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 044-339
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
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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