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Suspension System on Impingement Syndrome

Effect of a Selected Suspension System Exercise Program on Patients With Subacromial Impingement Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05955820
Enrollment
51
Registered
2023-07-21
Start date
2022-09-21
Completion date
2023-07-08
Last updated
2023-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Impingement Syndrome

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.

Interventions

Participants will be tested by four exercises designed for impingement syndrome using the suspension system

DEVICEDumbbells

Participants will be tested by four exercises designed for impingement syndrome using Dumbbells

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Improvement in active shoulder ROMBaselineProprioception 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 performanceBaselineAssessment 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

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026