- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05893628
Effect of Pectoralis Minor on Endurance
January 26, 2024 updated by: Emine Cihan, Selcuk University
Effect of Pectoralis Minor Length on Scapular Endurance and Core Endurance
The aim of this study evaluate the effects of dominant and non-dominant pectoralis minor (PM) length on scapular and core muscle endurance in the absence of scapular dyskinesia.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
93
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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Konya, Turkey, 42130
- Selcuk 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
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
healthy adult women
Description
Inclusion Criteria:
- volunteered to participate in the study
- and did not have scapular dyskinesia according to the evaluations made
Exclusion Criteria:
- did not want to participate in the study
- and those with previous neurological or orthopedic upper extremity disorders,
- pain problems in any part of their body,
- previous abdominal surgery,
- and had communication 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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
study group
|
Pectoralis Minor Length and muscle endurance evaluation
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pectoralis Minor Length and Index
Time Frame: 10 minutes
|
PM length was measured with a caliper.
The distance between the starting (origin) and ending (insertion) points of the PM muscle was measured, with the participant in supine position and the shoulder joint free.Pectoralis minor index (PMI) was obtained by dividing the PM length recorded in cm by the person's weight and multiplying the result by 100.
PMI was determined by dividing the obtained value by weight
|
10 minutes
|
|
Scapular Dyskinesia
Time Frame: 15 minutes
|
The lateral scapular slide test (LSST) was used to evaluate scapular dyskinesia.
The distance between the inferior angle of the scapula and the closest vertebral spinous process in the standing upright position was bilaterally measured using a tape measure in three different positions
|
15 minutes
|
|
Scapular Muscle Endurance
Time Frame: 10 minutes
|
Scapular muscle endurance was evaluated with the scapular isometric compression test.
The participants were asked to stand upright with their arms on their sides and bring both shoulder blades closer together by maintaining this position as long as they could
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10 minutes
|
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Core Muscle Endurance
Time Frame: 15 minutes
|
This evaluation was performed using McGill's torso muscular endurance test battery consisting of endurance tests in the trunk flexion, trunk extension (Sorensen), and right/left side bridge positions
|
15 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 1, 2023
Primary Completion (Actual)
April 1, 2023
Study Completion (Actual)
April 25, 2023
Study Registration Dates
First Submitted
May 25, 2023
First Submitted That Met QC Criteria
June 5, 2023
First Posted (Actual)
June 8, 2023
Study Record Updates
Last Update Posted (Actual)
January 29, 2024
Last Update Submitted That Met QC Criteria
January 26, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2023/05.25
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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