Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05548816
Other study ID # 15121993
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 30, 2022
Est. completion date January 20, 2023

Study information

Verified date March 2023
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In the available literature, there are no prevalence studies that show the incidence of subacromial impingement in swimmers in Egypt, this should be considered as it's one of the most commonly reported injuries worldwide in swimmers. There are also no available studies to show the difference in incidence of subacromial impingement between both genders in Egypt. This study is attempting to remedy both research deficits and to reduce the literature gap and to show the prevalence rate of this injury among Egyptian swimmers in different age groups, to help prevent its widespread and to provide data for further investigations. This study would give the Egyptian swimming federation and the Ministry of youth and sports a clear idea about the prevalence rate of swimmer's shoulder at different ages in Egyptian swimmers. Most importantly, this study is to provide the physiotherapy community in Egypt data about this injury, the rate of prevalence and how to prevent it and hopefully would help in further future studies and also to apply it in different countries.


Recruitment information / eligibility

Status Completed
Enrollment 405
Est. completion date January 20, 2023
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 12 Years to 25 Years
Eligibility 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 Design


Intervention

Other:
Handheld Dynamometer , Special tests and Modified DASH questionarre .
A mix of tools , special tests and questionarre to help in confirming the diagnosis of subacromial impingement.

Locations

Country Name City State
Egypt Nutrilife clinic Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary External / lnternal rotation ratio Measured by Handheld dynamometer 1 day
Primary Lift-off test 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. 1 day
Primary Neers test 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. 1 day
Primary Hawkins and kennedy test 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. 1 day
Primary Modified QuickDASH questionarre result 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
See also
  Status Clinical Trial Phase
Terminated NCT03913702 - Subacromial Methylprednisolone Versus Ketorolac for Shoulder Impingement Phase 2
Completed NCT05071469 - Comparison of Two Different Treatment Methods N/A
Active, not recruiting NCT04660682 - A Comparison of the Long Term Effects of the Traditional and Modified Posterior Shoulder Stretching Exercise in Subacromial Impingement Syndrome N/A
Completed NCT03186287 - Effectiveness of Eccentric and Concentric Strength Training in Patients With Subacromial Impingement Syndrome N/A
Completed NCT04915430 - Training in Subacromial Impingement Syndrome N/A
Recruiting NCT01691157 - Exercise in the Physiotherapy Management of Shoulder Impingement N/A
Completed NCT01753271 - Subacute Effects of Spinal Mobilization to Treat Subacromial Impingement N/A
Withdrawn NCT01449448 - Subacromial Injection With Corticosteroid Versus Nonsteroidal Anti-inflammatory Drugs (NSAID) in Shoulder Impingement Syndrome N/A
Not yet recruiting NCT05794633 - Acupuncture Therapy in Patients With Subacromial Impingement Syndrome N/A
Active, not recruiting NCT06324487 - A New Application in Subacromial Impingement Syndrome N/A
Not yet recruiting NCT06023914 - Analysis of the Effect of Neuromuscular Electro-stimulation on the Performance of Isometric Rotator Cuff Strength. Phase 2/Phase 3
Recruiting NCT04644042 - The Effect of Arthroscopic Subacromial Decompression in Patients Who Are Non-responders to Non-operative Treatment. N/A
Completed NCT05549674 - Copenhagen Cohort of Patients With Shoulder Pain
Completed NCT04594408 - Tranexamic Acid to Improve Arthroscopic Visualization in Shoulder Surgery Phase 4
Completed NCT03888586 - Comparison of Dry Needling and Deep Friction Massage in Patients With Subacromial Pain Syndrome N/A
Completed NCT03303001 - Comparison Between Subacromial Infiltrations N/A
Recruiting NCT03658707 - Validity and Reliability of the Turkish Version of the Functional Shoulder Score
Recruiting NCT02374125 - Teres Major Muscle and Subacromial Impingement Syndrome N/A
Active, not recruiting NCT03326466 - Muscle Function, Central Nervous System Sensitization, and Pain Profiling in Patients With Subacromial Pain (SAP-CNSS).
Completed NCT04169880 - Effects of High Intensity Laser Therapy (HILT) in Patients With Subacromial Impingement Syndrome N/A