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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05439525
Other study ID # P.t.Rec/012/003613
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 5, 2022
Est. completion date August 30, 2022

Study information

Verified date June 2022
Source Cairo University
Contact alshaymaa sh abd el-azeim, lecturer
Phone 01033771553
Email alshaymaa.shaaban@pt.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the aim of this study is to investigate the Effect of mulligan technique on sub-acromial space in patients with shoulder impingement syndrome


Description:

Shoulder Impingement Syndrome (SIS) is defined as the mechanical entrapment of the rotator cuff (mainly the supraspinatus tendon) or the sub-acromial bursa in the sub-acromial space between the humeral head and the acromion or coracohumeral ligament .It is typically exacerbate when the arm is elevated or when overhead throwing activities are performed . Mulligan technique is a type of manual therapy with hypoalgesic effects, increases joint ROM, enhances muscle function and treats specific pathologies. Mobilization with movement (MWM) can be defined as the application of a sustained passive accessory force / glide to a joint while the patient actively performs a task that was previously identified as being problem.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date August 30, 2022
Est. primary completion date August 30, 2022
Accepts healthy volunteers No
Gender All
Age group 30 Years to 55 Years
Eligibility Inclusion Criteria: age of patients from 30- 55 years old . Both Male and female. Shoulder pain and two out of four specified objective signs and symptoms: Positive Neer impingement test. Positive Hawkins-Kennedy impingement test. Painful or limitation of active shoulder elevation (flexion, abduction, scaption). Pain or limitation with the functional movement patterns of hand-behind-back or hand-behind-head. Exclusion Criteria: Systemic or neurological disorder. Adhesive capsulitis. Cervical radiculopathy. History of shoulder surgery. Corticosteroid injection within the past month Subjects who had received physical therapy treatment for their shoulder within the past three months.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
mulligan technique
The patient will be in sitting and the therapist stands on the contralateral side of pain, stabilizing the scapula posteriorly with one hand. The head of the humerus is translated posteriorly and laterally with the other hand, along the plane of the glenoid fossa. While the glide is sustained, the patient actively elevates their arm through the plane of abduction or scaption (elevation). Apply 6-10 repetitions in a set, with 3-5 sets in a treatment session the perform mobilization on acromioclavicular and sternoclavicular joint
conventional therapy
Flexibility exercises: enhance flexibility of the glenohumeral Posterior capsule, pectoralis muscle, and upper thoracic spine. Strengthen the rotator cuff and scapular stabilizers. Improve upper-quarter postural awareness

Locations

Country Name City State
Egypt Deraya university Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Other pressure pain threshold pressure algometer will be used to measure pressure pain threshold up to two weeks
Other shoulder function quick DASH will be used to measure shoulder function. DASH is a shortened version of the DASH questionnaire that uses 11 items to measure the degree of difficulty in performing various physical activities due to a shoulder, arm, or hand problem (6 items); the severity of pain and tingling (2 items); and the problem's effect on social activities, work, and sleep (3 items). up to two weeks
Primary sub-acromial space sub-acromial space will be measured by ultrasonography up to two weeks
Secondary shoulder range of movement shoulder range of motion will be measured by digital goniometer up to two weeks
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