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NCT Number: NCT07646899

The Effect of Unstable Loads on Scapular Kinematics and Muscle Activation During Overhead Press in Overhead Athletes With Subacromial Pain Syndrome

The research aims to compare the differences between stable and unstable load conditions during shoulder pressing in overhead athletes with SAPS and to compare the differences between SAPS and healthy athletes with stable and unstable load conditions.

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Observational

Primary location

National Yang Ming Chiao Tung University

Taipei, Taiwan

Location status: Recruiting

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

stable load shoulder press

Behavioral

Participants performed a shoulder press using a barbell loaded at their individual 15-repetition maximum

Unstable load shoulder press

Behavioral

Participants performed a shoulder press using a unstable loaded at their individual 15-repetition maximum

Primary outcomes

  1. Scapular kinematics (degrees) during shoulder elevation measured by VIPER™ system

    Time frame: Immediately after the single session

    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.

  2. Surface electromyography (TeleMyo2400T G2, Noraxon USA Inc., Scottsdale, AZ, USA)

    Time frame: Immediately after the single session

    Muscle activation of upper trapezius, lower trapezius, serratus anterior, anterior deltoid, biceps brachii, triceps brachii, rectus abdominis, erector spinae during shoulder press

  3. Barbell trajectory (measured with camera)

    Time frame: Immediately after the single session

    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.

Secondary outcomes

  1. Shoulder average pain intensity

    Time frame: Immediately after the single session

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Yi Chung Tsai, Master

CONTACT

[email protected]

(886)972877917

Sponsors and collaborators

Lead sponsor

National Yang Ming Chiao Tung University

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Jun 15, 2026
Registry last updated
Jun 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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