Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:37 PM
Ignite Modification Date:
2025-12-24 @ 11:37 PM
NCT ID:
NCT07005856
Eligibility Criteria:
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
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT07005856
Study Brief:
Protocol Section:
NCT07005856