- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04687696
Comparison of The Effects of Different Stretching Techniques in Overhead Athletes
January 9, 2023 updated by: Gonca Şahiner Pıçak, Dokuz Eylul University
Comparison of The Effects of Different Stretching Techniques in Overhead Athletes With Glenohumeral Internal Rotation Deficit
78 overhead athletes with Glenohumeral Internal Rotation Deficit (GIRD) will be included in this study.
Participants will be randomly divided into 3 different groups of 26 people.
In each group will be applied posterior shoulder stretching exercises (PSSE) performed with different Muscle Energy Techniques (MET).
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Post Isometric Relaxation Group (PIRG) participants will perform a PSSE with post isometric relaxation (PIR) technique, Isolytic Stretching Group (ISG) participants will perform a a PSSE with isolytic stretching technique and Static Stretching Group Group (SSG) participants will perform a PSSE with static stretching technique.
All exercises will be performed in the modified crossbody position, for 5 times a week total of 6 weeks.
Subacromial space, posterior capsule and muscle tendon thicknesses will be measured using a 7-12 MHz linear transducer with USG (LOGIQ e Ultrasound, GE Healthcare, USA).
Athletes' GIRD results and rotational ROM measurements and Posterior shoulder tightness will be measured and recorded using a bubble inclinometer (Fabrication End Inc, New York, USA).
Scapula kinematics (posterior tilt, upward rotation) will be evaluated with a digital inclinometer.
Shoulder and scapular muscles will be evaluated with hend held dynamometer.
Tightness of Levator scapulae and pectoralis minor will be assessed.
The upper extremity functional performance of the athletes will be evaluated with the Functional Throwing Performance Index (FTPI).
Evaluations will be performed before training program and repeated after 6 weeks of training, and at the 1st, 3th and 6th months after training program is completed and the effects of different muscle energy techniques (MET) will be compared.
Investigators hypothesized 6 weeks of PSSE with different MET would have different effects on Acromio-Humeral Distance, posterior capsule thickness, muscle tendon thickness, rotational ROM measurements, scapula kinematics, muscle strength, posterior shoulder tightness and performance on overhead athletes with GIRD and the effects of MET would be superior to static stretching.
Study Type
Interventional
Enrollment (Anticipated)
78
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: Gonca Şahiner Pıçak, MSc
- Phone Number: +905058081268
- Email: gncshnr@gmail.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
13 years to 40 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Being overhead athlete
- Glenohumeral internal rotation range of motion of the affected shoulder should be less than other shoulder and bilateral shoulder internal rotation range of motion difference should be ≥15 º
Exclusion Criteria:
- Shoulder pain required medical attention for the last year.
- Current shoulder pain
- Cervical pain during upper extremity movement
- History of fracture to the shoulder girdle
- Systemic musculoskeletal disease
- History of shoulder surgery,
- Glenohumeral instability (positive apprehension, relocation, or positive sulcus test) or positive findings for a full thickness rotator cuff tear (positive lag sign, positive drop arm test, or marked weakness with shoulder external rotation)
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: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Post Isometric Relaxation Group
The participants in this group will perform post isometric relaxation stretching in modified cross body position for 6 weeks.
|
Athletes will be positioned in a modified cross-body position.
They will be asked to actively bring their underlying arm in the direction of horizontal adduction up to the physiological barrier barrier.
The participants will be asked to perform an isometric contraction for 5 seconds in the horizontal abduction direction with 20% of the maximum muscle strength.
After the relaxation, the arm will be moved towards horizontal adduction and 15 seconds active-assistive stretching will be applied.
Participants will be given a 5-second rest period between contractions.This stretching exercise will be applied in 5 repetitions in one session for 6 weeks 5 times a week.
|
|
Experimental: Isolytic Stretching Group
The participants in this group will perform isolytic stretching in modified cross body position for 6 weeks..
|
Athletes will be positioned in a modified cross-body position.
They will be asked to actively bring their underlying arm in the direction of horizontal adduction up to the physiological barrier barrier.
The participants will be asked to perform a contraction in the horizontal abduction direction with 20% of the maximum muscle strength.
When the muscle contraction occurs, the arm will be moved quickly in 2-4 seconds towards horizontal adduction and 15 seconds active-assistive stretching will be applied.
Participants will be given a 5-second rest period between stretches.
This stretching exercise will be applied in 5 repetitions in one session for 6 weeks 5 times a week.
|
|
Experimental: Static Stretching Group Group
The participants in this group will receive static stretching in modified cross body position for 6 weeks.
|
Athletes will be positioned in a modified cross-body position.
They will be asked to actively bring their underlying arm in the direction of horizontal adduction up to the physiological barrier.
Then, the arm will be moved towards horizontal adduction and 15 seconds active-assistive stretching will be applied.
Participants will be given a 5-second rest period between stretching exercises.
This stretching exercise will be applied in 5 repetitions in one session for 6 weeks 5 times a week.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shoulder internal rotation range of motion
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Change of shoulder internal rotation range of motion (with bubble inclinometer)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Subacromial space
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Change of subacromial space ( with Ultrasound)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
|
Posterior shoulder tightness
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Change of posterior shoulder tightness (with bubble inclinometer)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
|
Shoulder Total rotation range of motion
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Change of shoulder internal rotation + external rotation range of motion (with bubble inclinometer)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
|
Functional Throwing Performance Index
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Participants will throw a ball to shot a frame on a wall.
Number of correct shots will be recorded.
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
|
Posterior capsule thickness
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Change of posterior capsule thickness ( with Ultrasound)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
|
Muscle tendon thickness
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Change of supraspinatus, infraspinatus and teres minor tendon thicknesses ( with Ultrasound)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
|
Scapula kinematics
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Posterior tilt and upward rotation of the scapula during arm elevation (with digital inclinometer)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
|
Muscle Shortness
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Levator scapula and pectoralis minor shortness (with caliper and tape measure)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
|
Eccentric strength
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Change of shoulder abduction and external rotation eccentric strength (in kg, with hand held dynamometer)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
|
Isometric strength
Time Frame: baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Change of lower trapezius muscle, serratus anterior and rotator cuff muscles isometric strength (in kg, with hand held dynamometer)
|
baseline, 6 weeks of training, at the 1st, 3th and 6th months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Sevgi S Yeşilyaprak, Phd, Dokuz Eylül 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 (Anticipated)
February 1, 2023
Primary Completion (Anticipated)
February 1, 2024
Study Completion (Anticipated)
December 1, 2024
Study Registration Dates
First Submitted
December 22, 2020
First Submitted That Met QC Criteria
December 27, 2020
First Posted (Actual)
December 29, 2020
Study Record Updates
Last Update Posted (Estimate)
January 10, 2023
Last Update Submitted That Met QC Criteria
January 9, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 5003-GOA
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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