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

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

      • Konya, Turkey, 42130
        • Selcuk 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

  • 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

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
10 minutes
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.

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

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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