Suspension System on Impingement Syndrome

Not Applicable

Completed

• Conditions: Impingement Syndrome

• Registration Number: NCT05955820
• Lead Sponsor: Cairo University

Brief Summary

To investigate the effect of shoulder exercise using a selected suspension system exercise program on pain, disability, functional performance and proprioception in patients with subacromial impingement syndrome.

Detailed Description

Two groups were assigned to this study, the first one received four conventional exercises that designed for shoulder impingement syndrome, the second group received the same four conventional exercises plus four selected suspension system exercises.

The sessions were conducted three times per week fir four weeks.

Study Timeline

• Study Start: 2022-09-21
• Primary Completion: 2023-06-23
• Status Verified: 2023-07
• Study Completion: 2023-07-08
• Study First Submitted: 2023-07-08
• Study First Submitted QC: 2023-07-13
• Last Update Submitted: 2023-07-13
• Study First Posted: 2023-07-21
• Last Update Posted: 2023-07-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 51

Inclusion Criteria

1. Fifty-eight subjects with SIS (more than three months).
2. Their age ranges from 20-45 years old
3. Level of pain (at least 2/10 on VAS)
4. Body mass index (BMI) between 18-25
5. Subjects must show positive results in at least two of the following tests: Neer's impingement test, Hawkins-Kennedy test, supraspinatus (empty can) test, apprehension and relocation test.

Exclusion Criteria

The subjects will be excluded if they had:

1. Received physiotherapy at last 3 months.
2. Received corticosteroids injection in subacromial space at last 3 months.
3. Received anti-inflammatory medications.
4. Have a fracture or dislocation in shoulder, neck and thoracic regions.
5. Have an acute rotator cuff tear.
6. Have tumor or malignancy in shoulder region.
7. Have neurologic problems in shoulder, neck and thoracic regions.
8. Have cooperation difficulties due to cognitive disorders.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Improvement in active shoulder ROM	Baseline	Proprioception will be tested by using inclinometer to determine patient's active shoulder range of motion for internal and external rotation, flexion, and extension
Improvement in functional performance	Baseline	Assessment of function using SPADI subscale which contains 13 items that assess two domains; a 5-item subscale that measures pain and 8-item subscale that measures disability. In addition, Several non-specific strength/power tests may assist in determining the level of functional performance of the patients

Trial Locations

Locations (1)

Cairo university faculty of physical therapy; 🇪🇬 Cairo, Egypt