Muscle Fatigue and Scapular Sensorimotor System

July 15, 2019 updated by: Yi-Fen Shih, National Yang Ming University
The aims of this study are to investigate the effects of scapular muscle fatigue on scapular joint position sense and neuromuscular performance (scapular muscle strength, the kinematics data and muscle activity of shoulder during scaption (arm elevation in the scapular plane)). The investigators hypothesize that scapular muscle fatigue would increase scapular reposition error and affect neuromuscular performance of the scapular during scaption.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan, 11221
        • National Yang Ming University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 38 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2017

Primary Completion (Actual)

August 11, 2017

Study Completion (Actual)

March 27, 2018

Study Registration Dates

First Submitted

February 16, 2017

First Submitted That Met QC Criteria

February 27, 2017

First Posted (Actual)

February 28, 2017

Study Record Updates

Last Update Posted (Actual)

July 29, 2019

Last Update Submitted That Met QC Criteria

July 15, 2019

Last Verified

July 1, 2019

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)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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