- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01962727
Scapular Dyskinesis: a Reliability and Validity Study of Comprehensive Classification Test
Study Design: Clinical measurement (cross-sectional)
Objectives: The purpose of this study was to investigate the reliability and validity of the novel scapular dyskinesis classification test.
Background: A visual-based clinical assessment with sufficient reliability and validity to identify scapular dyskinesis provides information for rehabilitation treatment.
Methods: A visual-based palpation method was evaluated by two independent physiotherapists in 60 subjects with unilateral shoulder pain to test reliability. This method classified the scapular movements during arm raising/lowing movements in scapular plane as single abnormal scapular patterns (inferior angle/ medial border/ superior border of scapula prominence and abnormal scapulohumeral rhythm) or mixed abnormal scapular patterns. Different patterns of scapular dyskinesis were also validated by corresponding alternation of the scapular kinematics and muscular activities assessed by electromagnetic motion-capturing system and surface electromyography (EMG).
Study Overview
Status
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Taipei, Taiwan
- Performance analysis laboratory
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- (1) they were from 18 to 50 years old and (2) they had unilateral shoulder pain around shoulder complex during activities.
Exclusion Criteria:
- history of shoulder dislocation, fracture, or shoulder surgery within past 1 year, or a history of direct contact injury to the neck if upper extremities within the past 1 month, scoliosis or excessive kyphosis, neurological disorders, body mass index (BMI)≧25, or demonstrate pain (VAS>3) during overall testing procedure.
Study Plan
How is the study designed?
Design Details
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Reliability of scapular dyskinesis test
Time Frame: 2 hours
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The inter-rater reliability for the comprehensive scapular dyskinesis classification test was described using percentage of agreement and κ coefficient. Rating of scapular dyskinesis was evaluated and classified into 8 patterns including(A) patterns I (B) patterns II (C) pattern III (D) pattern IV (E) pattern I+II (F) pattern II+III (G) pattern I+III (H) pattern I+II+III. |
2 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Validity of scapular dyskinesis test
Time Frame: 2 hours
|
Different patterns of scapular dyskinesis were validated by corresponding alternation of the scapular kinematics and muscular activities assessed by electromagnetic motion-capturing system and surface electromyography. To quantitatively characterize the scapular kinematics and muscular activities, the kinematic data at 30°, 60°, 90°, and 120° and EMG data at 0~30°, 30°~60°, 60°~90°, 90°~120°, and >120° in the raising and lowering phases of humeral movement in the scapular plane were used as dependent variables. Data from the same scapular dyskinesis pattern assessed by 2 raters were used for validity analysis. |
2 hours
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Collaborators and Investigators
Investigators
- Principal Investigator: Jiu-Jenq Lin, PhD, School and Graduate Institute of Physical Therapy, College of Medicine, National Taiwan University, 100 Taipei, Taiwan
Publications and helpful links
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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201112034RIB
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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