- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05548816
Prevalence of Subacromial Impingement Among Egyptian Swimmers
Prevalence of Subacromial Impingement Among Egyptian Swimmers a Cross Sectional Survey Study.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Cairo, Egypt, 11375
- Nutrilife clinic
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Egyptian swimmers , Age ranging from 12 - 25 as mentioned in the subgroups and this study will be taken as a one shot.
Swimmers will be collected from (Al-Ahly, Heliopolis, Shooting, El Shams, Al-zohour ,platinum , El-Nasr, Cairo ,Al-Maadi, Tala'ea Elgeish, Ittihad el shorta , El- Rowad ,Wadi-Degla, Shooting ,El Ghaba and El Geziera Sporting Clubs).
Description
Inclusion Criteria:
- 440 swimmers (males and females) , their age between 12 - 25.
- Professional swimmers only.
- Complain of anterior shoulder pain while swimming or elevation of shoulder.
- BMI will be ranged from (18.5 - 24.9 kg/m2 ).
- All swimmers are under supervision and psychologically, medically stable.
- All swimmers received a good explanation of the questionnaire and the given study.
Exclusion Criteria:
- Any swimmer who refuse to participate in the study
- Uncooperative swimmers.
- Unprofessional swimmers.
- Participants who play any other sports.
- Exclude any previous traumatic lesion.
- Exclude any form of shoulder instability.
- Take any medication that affects pain perception as NSAIDS.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Subgroup (1) Male
Includes swimmers from 12 to less than 14 years.
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A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
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Subgroup (2) Male
Includes swimmers from 14 to less than 16 years.
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A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
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Subgroup (3): Male
Includes swimmers 16 to less than 18 years.
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A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
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Subgroup (4) Male
Includes swimmers from 18 to less than 20 years
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A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
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Subgroup (5) Male
(1st Team) includes swimmers from 20 - 25 years.
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A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
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Subgroup (1) Female
Includes swimmers from 12 to less than 14 years.
|
A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
|
|
Subgroup (2) Female
Includes swimmers from 14 to less than 16 years.
|
A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
|
|
Subgroup (3) Female
Includes swimmers 16 to less than 18 years.
|
A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
|
|
Subgroup (4) Female
Includes swimmers from 18 to less than 20 years.
|
A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
|
|
Subgroup (5) Female
(1st Team) includes swimmers from 20 - 25 years.
|
A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lift-off test
Time Frame: 1 day
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This test is performed in a standing position, with the examiner observing and testing from standing behind the patient.
To perform this test, the patient is asked to place the back of the affected arm (dorsum of the hand) in the mid lumbar spine area.
The testing movement involves the patient performing internal rotation (IR), by lifting the hand off the back while the examiner places pressure on the hand.
The test is considered to be positive if the patient cannot resist, lift the hand off the back or if she/he compensates by extending the elbow and shoulder.
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1 day
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Neers test
Time Frame: 1 day
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Neer's sign In standing the patient's arm was passively elevated in the plane of the scapula while preventing rotation of the scapula.
Reproduction of pain at the anterior edge of the acromion/lateral deltoid was considered a positive response for impingement.
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1 day
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Hawkins and kennedy test
Time Frame: 1 day
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Hawkins and Kennedy test while sitting, with the elbow flexed to 90, the patient's shoulder was passively elevated to 90 in the sagittal plane and then forcefully rotated medially.
Pain indicated a positive test result.
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1 day
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Modified QuickDASH questionarre result
Time Frame: 1 day
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The QuickDASH is scored in two components: the disability/symptom section (11 items, scored 1-5) and the optional high performance sport/music or work modules (4 items, scored 1-5) .For Example in the disability / symptoms sections , at least 10 of the 11 items must be completed for a score to be calculated. The assigned values for all completed responses are simply summed and averaged, producing a score out of five.This value is then transformed to a score out of 100 by subtracting one and multiplying by 25 , measures scaled on a 0-100 scale. A higher score indicates greater disability. |
1 day
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External / lnternal rotation ratio
Time Frame: 1 day
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Measured by Handheld dynamometer
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1 day
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 15121993
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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Universidad Autonoma de Nuevo LeonCompletedSubacromial Impingement Syndrome | Rotator Cuff Impingement Syndrome | Subacromial BursitisMexico
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CHU de ReimsTerminatedSubacromial Impingement of the ShoulderFrance