- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03066102
Muscle Fatigue and Scapular Sensorimotor System
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taipei, Taiwan, 11221
- National Yang Ming University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- no shoulder, cervical, and thoracic spine pain within six months
- negative for subacromial impingement test
- normal range of motion of glenohumeral joint
Exclusion Criteria:
- history of dislocation, fracture, or surgery of shoulder joint
- history of central nervous system disorder, rheumatoid arthritis, shoulder osteoarthritis, or cervical radiculopathy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change From Baseline in Scapular Proprioception
Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
Test the ability of active re-position the scapula from neutral to 90% range of protraction, and elevation.
|
through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
Change From Baseline in Muscle Activation During Scapular Proprioception
Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
Test the ability of muscle activation (upper trapezius, lower trapezius, and serratus anterior) during active re-position the scapula from neutral to 90% range of protraction, and elevation. Muscle activation during active re-position would divide into muscle activation during maximum voluntary isometric contraction (MVIC), present in percent. |
through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change From Baseline in Scapular Muscle Strength
Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
use dynamometer to detect the force of maximum isometric voluntary contraction of upper trapezius, lower trapezius and serratus anterior
|
through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
Change From Baseline in Shoulder Kinematics Data During Shoulder Elevation in the Scapular Plane
Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
use Liberty to detect the motion of spine, humerus, and scapula during shoulder elevation in the scapular plane (scaption)
|
through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
Change From Baseline in Scapular Muscle Activity During Shoulder Elevation in the Scapular Plane
Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
Test the ability of muscle activity (upper trapezius, lower trapezius, and serratus anterior) during shoulder elevation in the scapular plane (scaption). Muscle activation during scaption would divide into muscle activation during maximum voluntary isometric contraction (MVIC), present in percent. |
through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
Change From Baseline in Scapular Muscle Recruitment Timing During Arm Elevation in Scapular Plane
Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
Test the ability of muscle onset timing (upper trapezius, lower trapezius, and serratus anterior) during shoulder elevation in the scapular plane (scaption). Onset timing was determined by EMG signals bigger than resting signals plus 3 times standard deviations. Origin was set at onset of kinematics data of glenohumeral joint. |
through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects
|
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
- YM105067E
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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