- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07646899
The Effect of Unstable Loads on Scapular Kinematics and Muscle Activation During Overhead Press in Overhead Athletes With Subacromial Pain Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Yi Chung Tsai, Master
- Phone Number: (886)972877917
- Email: sc969183@gmail.com
Study Locations
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Taipei, Taiwan
- Recruiting
- National Yang Ming Chiao Tung University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
The inclusion criteria for both the experimental and control groups were as follows: (1) amateur or recreational overhead athletes aged 18-40 years (e.g., volleyball, tennis, baseball); (2) sport participation history of more than 3 years; (3) weekly overhead sport participation of more than 4 hours; (4) ability to meet the minimum loading requirements of the equipment for both stable and unstable conditions, defined as a 15-repetition maximum (15RM) for stable shoulder press of ≥10 kg and unstable shoulder press of ≥8 kg.
The individual inclusion criteria for the experimental group were: (1) diagnosis of subacromial pain syndrome, defined as at least 3 positive findings out of 5 clinical tests (Painful Arc test, Neer impingement test, Empty Can test, Hawkins-Kennedy impingement test, and Resisted External Rotation test); (2) Visual Analogue Scale (VAS) score of ≤3 during shoulder press performance; (3) symptoms present on the dominant side.
The individual inclusion criteria for the control group were: absence of shoulder pain within the past 6 months, including no pain at the glenohumeral joint, acromioclavicular joint, sternoclavicular joint, scapulothoracic joint, or cervical spine.
The exclusion criteria were as follows: (1) history of surgical intervention for fracture or dislocation of the shoulder or elbow joint within the past 6 months; (2) direct trauma to the cervical spine or upper extremity within the past 1 month; (3) shoulder pain or neurological symptoms of cervical origin; (4) any condition preventing the completion of the experimental protocol; (5) bilateral shoulder pain.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Control group
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Participants performed a shoulder press using a barbell loaded at their individual 15-repetition maximum
Participants performed a shoulder press using a unstable loaded at their individual 15-repetition maximum
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Experimental group
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Participants performed a shoulder press using a barbell loaded at their individual 15-repetition maximum
Participants performed a shoulder press using a unstable loaded at their individual 15-repetition maximum
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Scapular kinematics (degrees) during shoulder elevation measured by VIPER™ system
Time Frame: Immediately after the single session
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Scapular upward rotation, posterior tilt, and external rotation angles (in degrees) were recorded during shoulder press using the VIPER™ electromagnetic tracking system.
Data were collected at 30°, 60°, 90°, and 120° of humeral elevation, and reported as mean values for each angle.
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Immediately after the single session
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Surface electromyography (TeleMyo2400T G2, Noraxon USA Inc., Scottsdale, AZ, USA)
Time Frame: Immediately after the single session
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Muscle activation of upper trapezius, lower trapezius, serratus anterior, anterior deltoid, biceps brachii, triceps brachii, rectus abdominis, erector spinae during shoulder press
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Immediately after the single session
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Barbell trajectory (measured with camera)
Time Frame: Immediately after the single session
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The trajectory was captured by attaching reflective markers to the end of the barbell and recording kinematic data at a sampling frequency of 60 Hz using a camera.
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Immediately after the single session
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Shoulder average pain intensity
Time Frame: Immediately after the single session
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Pain is measured with Visual Analogue scale (VAS) Score range from 0 to 10. Scoring of 0 represents no pain and scoring of 10 represents pain as bad as it could possibly be.
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Immediately after the single session
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- NYCU113008AF
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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