- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06307899
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
Status
Recruiting
Conditions
Intervention / Treatment
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
- Name: Tuğçe Çoban, MSc
- Phone Number: +905454098540
- Email: fzttugce@yahoo.com
Study Locations
-
-
Çankaya
-
Ankara, Çankaya, Turkey, 06490
- Recruiting
- Gazi University
-
Contact:
- Tuğçe Çoban, MSc
- Phone Number: +905454098540
- Email: fzttugce@yahoo.com
-
-
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.
General Publications
- Borstad JD, Ludewig PM. Comparison of three stretches for the pectoralis minor muscle. J Shoulder Elbow Surg. 2006 May-Jun;15(3):324-30. doi: 10.1016/j.jse.2005.08.011.
- Rosa DP, Borstad JD, Pogetti LS, Camargo PR. Effects of a stretching protocol for the pectoralis minor on muscle length, function, and scapular kinematics in individuals with and without shoulder pain. J Hand Ther. 2017 Jan-Mar;30(1):20-29. doi: 10.1016/j.jht.2016.06.006. Epub 2016 Oct 18.
- Williams JG, Laudner KG, McLoda T. The acute effects of two passive stretch maneuvers on pectoralis minor length and scapular kinematics among collegiate swimmers. Int J Sports Phys Ther. 2013 Feb;8(1):25-33.
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
Keywords
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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