Immediate Effects of Different Stretching Methods for Pectoralis Minor Muscle

March 6, 2024 updated by: Tuğçe Çoban, Gazi University

Comparison of Immediate Effects of Different Stretching Methods for Pectoralis Minor Muscle on Scapula Position, Pectoralis Minor Muscle Length and Scapular Muscle Activation in Individuals With Shoulder Protraction

The aim of our study is to compare the effects of different stretching methods for the pectoralis minor (PM) muscle on scapula position, PM muscle length and scapular muscle activation in individuals with shoulder protraction. Unilateral corner stretching, manual stretching and proprioceptive neuromuscular facilitation (PNF) stretching methods will be applied randomly, 2 days apart, to volunteer individuals who agree to participate in our study. Three different stretching methods (unilateral corner stretching, manual stretching and PNF stretching) will be applied to individuals randomly, 48 hours apart, and PM length, PM index, scapula upward rotation and EMG values will be recorded by a blind evaluator before and after the stretching application.

Study Overview

Detailed Description

Our study will include individuals who volunteer to participate in the study, and informed consent will be obtained from the individuals. Shoulder protraction will be determined according to the measurement result of the distance between the posterolateral side of the acromion and the bed in the supine position of the individual. If the distance is 2.6 centimeters or more, it will be recorded as shoulder protraction posture. PM length, PM index, upward rotation angle of the scapula at 0°, 45°, 90° and 135° abduction, electromyographic (EMG) muscle activation of the upper trapezius, middle trapezius, lower trapezius and serratus anterior muscles will be evaluated by a blind evaluator before and after the stretching methods. Unilateral corner stretching, manual stretching and proprioceptive neuromuscular facilitation (PNF) stretching methods will be applied randomly, 48 hours apart. The order of Unilateral Corner Stretching, Manual Stretching and PNF Stretching methods to be applied to individuals will be assigned with the simple allocation using random allocation. SPSS (Statistical Package for Social Sciences) version 22.0 will be used to evaluate the data obtained from the study and create tables. The Shapiro-Wilk test will be used to determine the distribution of the data. Descriptive statistics of numerical variables with normal distribution will be indicated by X ± SD, descriptive statistics of numerical variables without normal distribution will be indicated by median and (IQR), descriptive statistics of categorical variables will be indicated by frequency and percentage (%). Paired Sample T test will be used for intra-group comparison of normally distributed data and Wilcoxon test will be used for intra-group comparison of non-normally distributed data. The one-way repeated measures analysis of variance (ANOVA) will be performed to compare the three groups. The statistical significance level will be set at p<0.05 and a post-hoc multiple comparisons test with Bonferroni correction will be performed.

Study Type

Interventional

Enrollment (Estimated)

25

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 Contact

Study Locations

    • Çankaya
      • Ankara, Çankaya, Turkey, 06490
        • Recruiting
        • Gazi University
        • Contact:

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

Description

Inclusion Criteria:

  • Having a shoulder protraction posture
  • Not having had a shoulder surgery before
  • Agreeing to participate in the study

Exclusion Criteria:

  • Cervical or shoulder pain
  • Adhesive capsulitis
  • Thoracic outlet syndrome
  • Shoulder instability
  • Shoulder surgery history
  • Numbness or tingling in the upper extremity

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group 3
PNF Stretching
Individuals will be in a sitting position with their hands clasped behind the head. The PM muscle will be stretched in the direction of horizontal abduction by placing the physiotherapist's hands anterior to the elbows. Passive stretching will be continued for 10 seconds, followed by 6 seconds of maximum voluntary isometric contraction of the PM muscle. The procedure will be repeated four times with 30 seconds of rest.
Experimental: Group 1
Unilateral Corner Stretching
Individuals will be positioned in a standing position with the elbow in 90° flexion and the shoulder in 90° abduction, placing the palm on a flat surface. For stretching, individuals will be asked to increase shoulder horizontal abduction by rotating the trunk anteriorly and contralaterally. The position will be maintained for 30 seconds and will be repeated 4 times with a 30-second rest between repetitions.
Experimental: Group 2
Manual Stretching
Individuals will be positioned supine with the shoulder in 90º abduction and external rotation and the elbow in 90º flexion. Stretching will be applied by the physiotherapist from just distal to the elbow in the direction of horizontal abduction of the shoulder. The position will be maintained for 30 seconds and will be repeated 4 times with a 30-second rest between repetitions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pectoralis Minor Length
Time Frame: Baseline
To measure the length of the pectoralis minor muscle, the distance between the caudal corner of the 4th rib and the inferomedial face of the coracoid process will be recorded with a tape measure.
Baseline
Pectoralis Minor Length
Time Frame: Immediately after intervention
To measure the length of the pectoralis minor muscle, the distance between the caudal corner of the 4th rib and the inferomedial face of the coracoid process will be recorded with a tape measure.
Immediately after intervention
Pectoralis Minor Index
Time Frame: Baseline
PM index will be recorded by calculating the ratio of the pectoralis minor length to the individual's height multiplied by 100.
Baseline
Pectoralis Minor Index
Time Frame: Immediately after intervention
PM index will be recorded by calculating the ratio of the pectoralis minor length to the individual's height multiplied by 100.
Immediately after intervention
Scapula Upward Rotation Measurement
Time Frame: Baseline
Individuals' scapula upward rotation measurement will be evaluated with an inclinometer in the resting position, 45º, 90º and 135º shoulder abduction positions. Three measurements will be taken with a 30-second rest interval and the average value will be calculated.
Baseline
Scapula Upward Rotation Measurement
Time Frame: Immediately after intervention
Individuals' scapula upward rotation measurement will be evaluated with an inclinometer in the resting position, 45º, 90º and 135º shoulder abduction positions. Three measurements will be taken with a 30-second rest interval and the average value will be calculated.
Immediately after intervention
EMG Analysis
Time Frame: Baseline
Individuals' upper trapezius, middle trapezius, lower trapezius and serratus anterior muscle activations will be evaluated using superficial EMG. Measurements will be taken from the dominant side.
Baseline
EMG Analysis
Time Frame: Immediately after intervention
Individuals' upper trapezius, middle trapezius, lower trapezius and serratus anterior muscle activations will be evaluated using superficial EMG. Measurements will be taken from the dominant side.
Immediately after intervention

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: Selda Başar, PhD, Gazi University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

September 11, 2023

Primary Completion (Estimated)

July 3, 2024

Study Completion (Estimated)

September 4, 2024

Study Registration Dates

First Submitted

March 6, 2024

First Submitted That Met QC Criteria

March 6, 2024

First Posted (Actual)

March 13, 2024

Study Record Updates

Last Update Posted (Actual)

March 13, 2024

Last Update Submitted That Met QC Criteria

March 6, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • E-77082166-302.08.01-639069

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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