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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01962727
Other study ID # 201112034RIB
Secondary ID
Status Completed
Phase N/A
First received August 12, 2013
Last updated October 10, 2013
Start date March 2012
Est. completion date October 2012

Study information

Verified date October 2013
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

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).


Description:

No other detailed description


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date October 2012
Est. primary completion date October 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 50 Years
Eligibility 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 Design

Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Performance analysis laboratory Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reliability of scapular dyskinesis test The inter-rater reliability for the comprehensive scapular dyskinesis classification test was described using percentage of agreement and ? 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 No
Secondary Validity of scapular dyskinesis test 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 No