- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06704529
Cortical Processing of Proprioception Related to Pitching Performance in Baseball Players With Glenohumeral Internal Rotation Deficit
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Taiwan
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Taipei, Taiwan, Taiwan, 100
- Institute of Physical Therapy, National Taiwan University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- playing baseball for at least one year
- still active in training or competition
- frequency of training or games should be at least 3 hours per week
Exclusion Criteria:
- current dominant upper extremities pain
- a history of upper extremities surgical interventions or fractures or dislocation or degenerative joint disease
- cervical radiculopathy within 6 months
- lower extremities injury or surgery within the current 6 months
- Visual analog scale (VAS) > 5 during movement in the experiment
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
baseball players with GIRD
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participants pitch fastball to the strike zone
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baseball players without GIRD
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participants pitch fastball to the strike zone
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Active joint reposition test
Time Frame: baseline
|
Participants will mimic the pitching motion with reducing the influence from the lower limb by kneeling the knee and hip of the nondominant side 90° and their foot are flat on the ground.
They will be blindfolded, with their non-throwing hand resting on the thigh.
The reproducing arm-cocking and ball-release positions will be tested at random sequences for six trials, respectively.
Results or feedback regarding the accuracy of individual trials will not be provided at any time.
The acuity of active joint reposition will be calculated by 3-dimensional variable error scores for scapulothoracic (internal-external rotation, upward-downward rotation, posterior-anterior tilt) and glenohumeral (internal-external rotation, horizontal abduction-adduction, abduction-adduction) joint 55.
Three-dimensional variable error scores (3DVE) reflect acuity (measured in degrees) in all planes of motion measured for individual joints.
|
baseline
|
|
Pitching performance
Time Frame: baseline
|
Pitching performance will be collected by radar gun (JUGS company, Tualatin, OR, USA) and digital camera (JVC GC-PX100B, Yokohama, Japan) for ball velocity and pitching location, respectively. Participants will pitch on a mound 18.44 m away from the home plate. The target will be aligned with the theoretical line extending from the right edge of the home plate at a height of approximately 30 cm above the ground. After warming up at their own pace, each participant throws 30 game-like effort pitches in three 10-pitch sessions without specific instruction on focusing their attention. The fastest velocity of 10 pitches will be collected for analysis. |
baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shoulder range of motion
Time Frame: baseline
|
The tester grasps the subject's forearm in a supine position to measure the shoulder horizontal adduction/abduction. The humerus will be moved until the movement ceases (firm end-feel), indicating the end of shoulder tissue flexibility. The recorder places the digital inclinometer parallel to the humerus. Each measurement will be performed 3 times, and the average data will be analyzed. GH internal/external (IR/ER) ranges will be measured accordingly following the method in a previous study. Participants lay down supine with 90° shoulder abduction and elbow flexion. Then GH IR/ER will be measured by the main assessor using a digital inclinometer by stabilizing the scapula by grasping the coracoid process and the spine of the scapula posteriorly, then moving the forearm to reach the end range. Each measurement will be performed 3 times, and the average data will be used for analysis. |
baseline
|
|
Humeral retrotorsion
Time Frame: baseline
|
Humeral retrotorsion will be measured with the T3300 ultrasound system (BenQ, Taipei, Taiwan).
Participants lay supine with 90° shoulder abduction and elbow flexion.
The main assessor places the transducer on the participant's anterior shoulder for a short-axis view of the lesser and greater tubercles.
The two-person technique is adopted.
The first assessor adjusts the probe perpendicular to the floor and rotates the participant's humerus with a line connecting the greater and lesser tubercles parallel to the horizontal plane.
Then, the second assessor places a digital inclinometer on the ulnar side of the forearm to record the rotation angle, which is defined as the humeral retroversion.23
The ICC3,k of intra-rater reliability is 0.995.
Each measurement will be performed 3 times, and averaged data will be used for analysis.
|
baseline
|
|
Acromiohumeral distance
Time Frame: baseline
|
Acromiohumeral distance will be measured with the ultrasound transducer placed on the lateral aspect of the acromion in line with the longitudinal axis of the humerus to visualize the shortest distance between the humerus and the acromion.58
Three consecutive ultrasound images of the acromiohumeral distance are captured.
The investigator captures 3 more consecutive ultrasound images at rest while the participant sit with the shoulder in the neutral position.
The shortest distance will be measured with built-in calipers.
The ICC3,k for intra-rater reliability is 0.963.
Each measurement will be performed 3 times and averaged data will be used for analysis.
|
baseline
|
|
Rotator cuff thickness
Time Frame: baseline
|
The probe will be positioned on the bicipital grove horizontally to measure subscapularis tendon thickness in a short axis of view.
The participant's forearm is placed with the elbow flexed to 90° in slight internal rotation, with the palm facing upward and medially.
This position allows the bicipital groove to be brought to an anterior position, allowing clear visualization of the tendon within the grove. .
|
baseline
|
|
Posterior capsule thickness
Time Frame: baseline
|
For measurement of the posterior capsule thickness, the participants sit upright in a chair with both forearms resting on the thighs and upper arms by the participant's sides.
The examiner positions a transducer on the posterior shoulder and visualizes the glenoid labrum, humeral head, rotator cuff, and posterior capsule.
The posterior capsule is defined as the tissue immediately lateral to the tip of the labrum between the humeral head and rotator cuff.
When the capsule is identified in the image, posterior capsule thickness will be measured with built-in calipers.
The ICC3,k for intra-rater reliability is 0.951.
Each measurement will be performed 3 times, and averaged data will be used for analysis.
|
baseline
|
|
Kerlan-Jobe Orthopaedic Clinic Shoulder and Elbow score (KJOC)
Time Frame: baseline
|
The KJOC is the most common questionnaire for overhead athletes, and it was conducted in several studies.66
Recently, the Major League Baseball (MLB) organization adopted this evaluation tool as the standard for recovering injuries in MLB players.67
The questionnaire is commonly used to assess shoulder function and performance.
It is valid, reliable in its pilot form, and responsive to the tested population of adult overhead athletes.66
KJOC questionnaire ranges from 0 to 100, and the lower score represents a limited function.
|
baseline
|
|
Posterior capsule elasticity
Time Frame: baseline
|
To measure the posterior capsule elasticity, the participants sit upright in a chair with both forearms resting on the thighs and upper arms by the participant's sides.
The examiner positions a transducer on the posterior shoulder and visualizes the glenoid labrum, humeral head, rotator cuff, and posterior capsule.
The posterior capsule is defined as the tissue immediately lateral to the tip of the labrum between the humeral head and rotator cuff.
When the capsule is identified in the image, posterior capsule elasticity will be recorded.
Each measurement will be performed 3 times and averaged data will be used for analysis.
|
baseline
|
Collaborators and Investigators
Collaborators
Publications and helpful links
General Publications
- Ludewig PM, Cook TM. Alterations in shoulder kinematics and associated muscle activity in people with symptoms of shoulder impingement. Phys Ther. 2000 Mar;80(3):276-91.
- Mine K, Nakayama T, Milanese S, Grimmer K. Effectiveness of Stretching on Posterior Shoulder Tightness and Glenohumeral Internal-Rotation Deficit: A Systematic Review of Randomized Controlled Trials. J Sport Rehabil. 2017 Jul;26(4):294-305. doi: 10.1123/jsr.2015-0172. Epub 2016 Aug 24.
- Aldridge R, Stephen Guffey J, Whitehead MT, Head P. The effects of a daily stretching protocol on passive glenohumeral internal rotation in overhead throwing collegiate athletes. Int J Sports Phys Ther. 2012 Aug;7(4):365-71.
- Johnson JE, Fullmer JA, Nielsen CM, Johnson JK, Moorman CT 3rd. Glenohumeral Internal Rotation Deficit and Injuries: A Systematic Review and Meta-analysis. Orthop J Sports Med. 2018 May 22;6(5):2325967118773322. doi: 10.1177/2325967118773322. eCollection 2018 May.
- Meister K, Day T, Horodyski M, Kaminski TW, Wasik MP, Tillman S. Rotational motion changes in the glenohumeral joint of the adolescent/Little League baseball player. Am J Sports Med. 2005 May;33(5):693-8. doi: 10.1177/0363546504269936. Epub 2005 Feb 16.
- Astolfi MM, Struminger AH, Royer TD, Kaminski TW, Swanik CB. Adaptations of the Shoulder to Overhead Throwing in Youth Athletes. J Athl Train. 2015 Jul;50(7):726-32. doi: 10.4085/1062-6040-50.1.14. Epub 2015 Mar 26.
- Freehill MT, Archer KR, Diffenderfer BW, Ebel BG, Cosgarea AJ, McFarland EG. Changes in collegiate starting pitchers' range of motion after single game and season. Phys Sportsmed. 2014 Feb;42(1):69-74. doi: 10.3810/psm.2014.02.2049.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 202407026RINB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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