Effect Of Instrumented Assisted Soft Tissue Mobilization On Pain, Function And Proprioception In Patients With Shoulder Impingement Syndrome (SIS)

Cairo University (CU)

Status: Not yet enrolling

Conditions: Shoulder Impingement

Treatments: Other: instrumented assisted soft tissue mobilization; Other: traditional therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT05546177

p.t.REC/012/002833

Details and patient eligibility

About

this study will be conducted to investigate instrumented Assisted Soft Tissue Mobilization On Pain, Function And Proprioception In Patients With Shoulder Impingement Syndrome

Full description

Shoulder impingement is a clinical syndrome in which soft tissues become painfully entrapped in the area of the shoulder joint. Patients present with pain on elevating the arm or when lying on the affected side. Shoulder pain is the third most common musculoskeletal complaint in orthopedic practice, and impingement syndrome is one of the more common underlying diagnoses. On the pathophysiological level, it can have various functional, degenerative, and mechanical causes. The impingement hypothesis assumes a pathophysiological mechanism in which different structures of the shoulder joint come into mechanical conflict. The decision to treat conservatively or surgically is generally made on the basis of the duration and severity of pain, the degree of functional disturbance, and the extent of structural damage. The goal of treatment is to restore pain-free and powerful movement of the shoulder joint.Instrument-assisted soft tissue mobilization (IASTM) is a popular treatment for myofascial restriction which is applied using specially designed instruments to provide a mobilizing effect to soft tissue (e.g., scar tissue and myofascial adhesion) to decrease pain and improve range of motion (ROM) and function. eighty patients will be allocated randomly into two equal groups; the experimental one will receive IASTM and the control will receive traditional therapy for eight weeks.

Enrollment: 80 estimated patients

Sex: All

Ages: 25 to 40 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with impingement syndrome from both genders.
• Age range from 25-40 years
• Body mass index 18.5-24.9 kg/m2
• Subjects are non-smokers.
• Shoulder impingement symptoms lasting at least 6 weeks

Exclusion criteria

1. Hand truma, present pain or other kinds of complaints in the hand area.
2. History of deformities, fractures, or surgery of the tested upper extremity joints affecting hand grip strength within the last 6 months.
3. Presence of cardiopulmonary, hormonal disorder, central or peripheral neurological deficits or any condition that can influence the results.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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80 participants in 2 patient groups

instrumented assisted soft tissue mobilization

Experimental group

Description:

the patients will receive instrumented assisted soft tissue mobilization three times a week for eight weeks

Treatment:

Other: instrumented assisted soft tissue mobilization

Other: traditional therapy

traditional therapy

Active Comparator group

Description:

the patients will receive traditional therapy three times a week for eight weeks

Treatment:

Other: traditional therapy