- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02688205
Correlation Between Cyriax's Functional Examination and Ultrasound Examination in Patients With Shoulder Pain
Shoulder problems cause substantial disability in daily living, work, leisure activity, and exercise. The presence of shoulder problem such as rotator cuff pathology reported was highly predictive of impaired health-related quality of life.
Many tests were used for physical examination of the shoulder. The reliability and validity of the tests have been studied before. However, a systemic review concluded that there was conflicting evidence in reliability of each or combined tests. Functional examination of the shoulder by Cyriax is composed of a series of tests to evaluate a shoulder problem. It includes three arm elevation, three tests for glenohumeral joints, and six resisted tests.
As far as the investigators know, correlation of Cyriax functional examination with the ultrasonographic findings has never been reported before. Therefore, the aim of this study is to compare the clinical diagnosis by Cyriax's functional examination with ultrasound findings in patients with shoulder pain.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Taipei, Taiwan
- Shin Kong Wu Ho-Su Memorial Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Study group:
- patients with unilateral or bilateral shoulder pain with unknown causes;
- age≥ 20 years old.
Control group:
- patients without unilateral or bilateral shoulder pain;
- age≥ 20 years old.
Exclusion Criteria:
1) chronic inflammatory joint disease, infections or tumors of the shoulder, previous fracture or surgery of shoulder, and referred pain from cervical origin or visceral organs.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Shoulder pain group
The participants receive Cyriax's functional examination after history taking, and will be examined by ultrasound in one week.
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included active range of motion, passive range of motion, resisted test and accessory test for shoulder pain evaluation
to evaluate rotator cuff, acromio-clavicular joint, and subdeltoid-subacromial bursa
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Without shoulder pain group
The participants receive Cyriax's functional examination after history taking, and will be examined by ultrasound in one week.
|
included active range of motion, passive range of motion, resisted test and accessory test for shoulder pain evaluation
to evaluate rotator cuff, acromio-clavicular joint, and subdeltoid-subacromial bursa
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cyriax's functional examination for diagnosis
Time Frame: 1 week
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After Cyriax's functional examination for evaluating shoulder pain, a clinical diagnosis is made by the physician
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1 week
|
Ultrasound examination for diagnosis
Time Frame: 1 week
|
Ultrasound examination is done in one week after Cyriax's functional examination for detailed shoulder pathology evaluation.
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1 week
|
Collaborators and Investigators
Investigators
- Principal Investigator: Lin-Fen Hsieh, M.D., Shin Kong Wu Ho-Su Memorial Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
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
- 20140107R
- SKH-8302-103-DR-37 (Other Grant/Funding Number: Shin Kong Wu Ho-Su Memorial Hospital)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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