- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05439525
Effect of Mulligan on Sub-acromial Space in Patients With Shoulder Impingement Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Cairo, Egypt
- Deraya university
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Contact:
- Noha alaa eldeen Mahmoud
- Phone Number: 01092569170
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Contact:
- Amal Hassan Mohammed
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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 Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Group A
the patient will receive Shoulder complex mobilization with movement three time a week for two weeks
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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
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ACTIVE_COMPARATOR: Group B
will receive Conventional therapy three times a week for two weeks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
sub-acromial space
Time Frame: up to two weeks
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sub-acromial space will be measured by ultrasonography
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up to two weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
shoulder range of movement
Time Frame: up to two weeks
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shoulder range of motion will be measured by digital goniometer
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up to two weeks
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
pressure pain threshold
Time Frame: up to two weeks
|
pressure algometer will be used to measure pressure pain threshold
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up to two weeks
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shoulder function
Time Frame: up to two weeks
|
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).
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up to two weeks
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.t.Rec/012/003613
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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