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Clinical Trials/NCT07005856
NCT07005856CompletedNot Applicable

The Immediate Effects of Soft Tissue Mobilization on Shoulder Mobility, Pain, Scapular Kinematics and Muscle Activation and Muscle Stiffness in Symptomatic Overhead Athletes With Posterior Shoulder Tightness

National Yang Ming Chiao Tung University1 site in 1 country54 target enrollmentStarted: May 15, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
54
Locations
1
Primary Endpoint
Shoulder passive range of motion (measured with goniometer)

Study Overview

Brief Summary

The aim of this study is to investigate the immediate effects of soft tissue mobilization on shoulder mobility, pain, scapular kinematics and muscle activation and muscle Stiffness in symptomatic overhead athletes with posterior shoulder tightness.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Amateur overhead athletes aged 18-50 years.
  • •Participation in overhead sports training for more than 4 hours per week.
  • •Playing experience of more than 3 years.
  • •Shoulder range of motion deficits: internal rotation range of motion (ROM) on the affected side is at least 10 degrees less than the unaffected side, and total rotational ROM (internal rotation + external rotation) is at least 5 degrees less than the unaffected side, or horizontal adduction ROM is at least 10 degrees less than the unaffected side.
  • •Patients with subacromial pain syndrome: diagnosis requires at least 3 out of 5 positive test results (Hawkins-Kennedy impingement test, Neer impingement test, Empty Can test, Painful Arc test, and External Rotation Resistance test).

Exclusion Criteria

  • •Negative result on the kinetic medial rotation test.
  • •History of shoulder fracture, dislocation, or upper limb injury requiring surgery within the past 6 months.
  • •Inability to complete the experiment due to personal factors.
  • •Shoulder pain intensity greater than 7 points on the Visual Analog Scale (VAS).
  • •History of direct trauma to the neck or upper limb within the past month. Shoulder pain and neurological symptoms originating from the cervical spine. Contraindications to soft tissue mobilization, such as open wounds in the treatment area, skin cancer, localized infection, severe edema, vascular disorders, or acute muscle tears in the treatment area

Arms & Interventions

Stretching group

Experimental

Intervention: Stretching (Other)

Soft tissue mobilization group

Experimental

Intervention: Soft tissue mobilization (Other)

Hot pack group

Active Comparator

Intervention: Hot pack (Other)

Outcomes

Primary Outcomes

Shoulder passive range of motion (measured with goniometer)

Time Frame: Immediately after the single session

Shoulder external rotation, internal rotation, horizontal adduction range of motion in shoulder flexion 90 degrees

Shoulder active range of motion (measured with goniometer)

Time Frame: Immediately after the single session

Shoulder external rotation, internal rotation, horizontal adduction range of motion in shoulder flexion 90 degrees

Perceived improvement

Time Frame: Immediately after the single session

Perceived improvement was assessed through the GROC scale. Global Rating of Change (GROC) scale was used to assess the participant's perceived improvement. The scale ranges from -7 to +7, where -7 indicates a very great deal worse, 0 indicates no change, and +7 indicates a very great deal better. Higher scores reflect greater perceived improvement.

Shoulder muscle stiffness

Time Frame: Immediately after the single session

Mean dynamic muscle stiffness (N/m) of shoulder posterior muscles (deltoid, infraspinatus, teres minor) measured by MyotonPRO

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.

Secondary Outcomes

  • Surface electromyography (TeleMyo2400T G2, Noraxon USA Inc., Scottsdale, AZ, USA)(Immediately after the single session)
  • Scapular kinematics (degrees) during shoulder elevation measured by VIPER™ system(Immediately after the single session)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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