- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04687683
Comparison of Immediate Effects of Different Shoulder Stretching Techniques in Overhead Athletes
January 9, 2023 updated by: Gonca Şahiner Pıçak, Dokuz Eylul University
Comparison of Immediate Effects of Different Posterior Shoulder Stretching Techniques in Overhead Athletes With Glenohumeral Internal Rotation Deficits
81 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 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 cross-body position.
Subacromial space and posterior capsule thickness 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 will be measured and recorded using a bubble inclinometer (Fabrication End Inc, New York, USA).
The upper extremity functional performance of the athletes will be evaluated with the Functional Throwing Performance Index (FTPI).
Evaluations will be repeated tree times before, after the stretching exercise and 30 minutes later and the effects of different muscle energy techniques (MET) will be compared.
Investigators hypothesized PSSE made with different MET techniques have different effects on Acromio-Humeral Distance, posterior capsule thickness, rotational ROM measurements and performance on overhead athletes with GIRD and the effects of MET would be superior to static stretching.
Study Type
Interventional
Enrollment (Anticipated)
81
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Post Isometric Relaxation Group
The participants in this group will receive post isometric relaxation stretching in modified cross body position.
|
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 for one session.
|
|
Experimental: Isolytic Stretching Group
The participants in this group will receive isolytic stretching in modified cross body position.
|
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 for one session.
|
|
Experimental: Static Stretching Group Group
The participants in this group will receive static stretching in modified cross body position.
|
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 for one session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shoulder internal rotation range of motion
Time Frame: baseline measurements, 3 minutes and 30 minutes
|
Change of shoulder internal rotation range of motion (with bubble inclinometer)
|
baseline measurements, 3 minutes and 30 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Subacromial space
Time Frame: baseline measurements, 3 minutes and 30 minutes
|
Change of subacromial space ( with Ultrasound)
|
baseline measurements, 3 minutes and 30 minutes
|
|
Posterior capsule thickness
Time Frame: baseline measurements, 3 minutes and 30 minutes
|
Change of posterior capsule thickness ( with Ultrasound)
|
baseline measurements, 3 minutes and 30 minutes
|
|
Functional Throwing Performance Index
Time Frame: baseline measurements, 3 minutes and 30 minutes
|
Participants will throw a ball to shot a frame on a wall.
Number of correct shots will be recorded
|
baseline measurements, 3 minutes and 30 minutes
|
|
Shoulder Total rotation range of motion
Time Frame: baseline measurements, 3 minutes and 30 minutes
|
Change of shoulder internal rotation + external rotation range of motion (with bubble inclinometer)
|
baseline measurements, 3 minutes and 30 minutes
|
|
Posterior shoulder tightness
Time Frame: baseline measurements, 3 minutes and 30 minutes
|
Change of posterior shoulder tightness (with bubble inclinometer)
|
baseline measurements, 3 minutes and 30 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 (Anticipated)
February 1, 2023
Primary Completion (Anticipated)
February 1, 2024
Study Completion (Anticipated)
December 1, 2024
Study Registration Dates
First Submitted
December 15, 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
- 5002-GOA
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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