- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05000177
Alterations in Central Control of Shoulder Muscles in Office Workers With Non-specific Chronic Neck Pain
September 18, 2022 updated by: Yin-Liang Lin, National Yang Ming University
Alterations in Corticospinal and Neuromuscular Control of Shoulder Complex in Office Workers With Non-specific Chronic Neck Pain
Non-specific chronic neck pain (NCNP) is commonly seen in office workers.
Individuals with NCNP not only demonstrate impaired neck movement control and muscle activation, but also show abnormal scapular kinematics and muscle activation timing.
Office workers with NCNP also show higher activity of upper trapezius during computer typing and have difficulty relaxing upper trapezius after typing.
These changes related to scapula may increase strain over neck.
In addition to the altered neuromuscular control, recent studies found neuroplasticity changes in the central nervous system on patients of chronic musculoskeletal disorders.
Therefore, few studies found shifts and alterations of motor cortex representation of neck muscles in individuals with NCNP, which was correlated with delayed muscle activation of deep neck flexors muscle in functional activities.
However, no studies have explored that whether this corticospinal adaptation also happens over scapular muscles, especially after a computer typing task.
The objectives of this proposal are to investigate the differences in corticospinal and neuromuscular control of shoulder complex between office workers with and without NCNP.
Thirty-five individuals with NCNP and 35 healthy controls will be recruited.
Twenty young healthy subjects will be also recruited for a pilot study to test the reliability of all the measures.
Scapular kinematics and muscle activation will be tested during arm elevation.
Corticospinal parameters of trapezius and serratus anterior will be tested with transcranial magnetic stimulation (TMS), including active motor threshold, motor evoked potential, cortical silent period, short interval intracortical facilitation, short interval intracortical inhibition and cortical mapping.
Corticospinal parameters, except cortical mapping, will be measured again after a 30-minute computer typing task.
Scapular muscle activation will be also recorded during the typing task.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
51
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
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Taipei, Taiwan, 112
- National Yang-Ming University
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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
20 years to 40 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria of Patients with Non-specific Chronic Neck Pain
- Ages ranges from 20-40 years old
- Work with the computer at least 25 hours per week
- Neck pain of idiopathic origin ≥ 6 months during the past year
- Minimum of 3/10 on the numerical rating scale (NRS) in past 7 days
No structural abnormalities which are confirmed by neck X-ray or negative results of all the following special tests
- Exclude nerve root compression: Cervical distraction test and Spurling's test
- Exclude cervical radiculopathy: Valsalva test
- Exclude cervical instability: Alar ligament test and Sharp-Purser test
- Specific head movements or maintaining the fixed posture for a long time reproduced neck pain
Inclusion Criteria of Healthy Subjects in the control group
- Ages ranges from 20-40 years old
- Work with the computer at least 25 hours per week
- No history of neck and/or shoulder pain sustained over one week in the past one year
Inclusion Criteria of Healthy subjects in the Pilot Study
- Ages ranges from 20-40 years old
- No history of neck and/or shoulder pain sustained over one week in the past one year
Exclusion Criteria of Patients with Non-specific Chronic Neck Pain and All Healthy Subjects)
- Any known pathology or impairment in the shoulder joint, which is the origin of neck pain
- Current episode of neck pain related to a traumatic event (e.g., whiplash injury)
- Have a history of cervical and/or shoulder pathology (e.g., fracture, dislocation, trauma, surgery of spinal or shoulder joint, inflammatory disease, frequent headache or dizziness)
- Brain injury and neurological impairment (e.g., radiculopathy, myelopathy or stroke)
- Systematic diseases (e.g., rheumatoid arthritis, ankylosing spondylitis), fibromyalgia, tumor
- Contraindications to the use of transcranial magnetic stimulation (TMS), assessed with a safety screening questionnaire, including pregnancy, history of seizure, epilepsy and syncope, having cochlear implant, having medal implant and taking anti-depressant medication
- Any kind of previous manual and/or movement therapy on upper extremity and neck during in recent 3 months
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Other: Experimental group: Non-specific chronic neck pain group
Subjects with non-specific chronic neck pain will be included to perform 30-minute computer typing task and assess neurophysiological measurements of scapular muscles, scapular kinematics and muscle activation.
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The subject sits in front of a computer screen and perform computer typing tasks for 30 minutes.
The same computer table and chair were used for all subjects.
The height of the table and screen, and the distance of the keyboard from the subject were adjusted according to their familiar and comfortable position.
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Other: Control group: Healthy subjects group
Healthy subjects will be included to compare the differences in neurophysiological measurements of scapular muscles, scapular kinematics and muscle activation between healthy subjects and subjects with non-specific chronic neck pain.
Subjects in this group will received the same assessment as the NCNP group.
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The subject sits in front of a computer screen and perform computer typing tasks for 30 minutes.
The same computer table and chair were used for all subjects.
The height of the table and screen, and the distance of the keyboard from the subject were adjusted according to their familiar and comfortable position.
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Other: Pilot study: Healthy subjects group
Healthy subjects will be included to test reliability of single-pulse and paired-pulse TMS, including its associated neurophysiological measurements, and also to test reliability of Liberty electromagnetic tracing system and surface electromyography.
Subjects in this group will received the same assessment as the NCNP group.
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Rest for 30 minutes
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Neurophysiological measures - Active motor threshold
Time Frame: Change from baseline AMT after 30-minute computer typing task or 30-minute rest
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Active motor threshold (AMT) will be described with the percentage (%) of maximum stimulator output (MSO).
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Change from baseline AMT after 30-minute computer typing task or 30-minute rest
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Neurophysiological measures - Motor evoked potential
Time Frame: Change from baseline MEP after 30-minute computer typing task or 30-minute rest
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Motor evoked potential (MEP) will be described with millivolt (mV).
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Change from baseline MEP after 30-minute computer typing task or 30-minute rest
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Neurophysiological measures - Cortical silent period
Time Frame: Change from baseline CSP after 30-minute computer typing task or 30-minute rest
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Cortical silent period (CSP) will be measured with millisecond (ms)
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Change from baseline CSP after 30-minute computer typing task or 30-minute rest
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Neurophysiological measures - Short interval cortical inhibition
Time Frame: Change from baseline SICI after 30-minute computer typing task or 30-minute rest
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Short interval cortical inhibition (SICI) will be defined as percentage (%) of conditioning responses vs testing responses while the inter-stimulus interval is below 5 ms
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Change from baseline SICI after 30-minute computer typing task or 30-minute rest
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Neurophysiological measures - Short interval cortical facilitation
Time Frame: Change from baseline SICF after 30-minute computer typing task or 30-minute rest
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Short interval cortical facilitation (SICF) will be defined as percentage (%) of conditioning responses vs testing responses while the inter-stimulus interval is above 5 ms
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Change from baseline SICF after 30-minute computer typing task or 30-minute rest
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Neurophysiological measures - Area of cortical mapping
Time Frame: Before 30-minute computer typing task
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Area of cortical mapping will be described with square millimeter (mm2)
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Before 30-minute computer typing task
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Neurophysiological measures - Volume of cortical mapping
Time Frame: Before 30-minute computer typing task
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Volume of cortical mapping will be calculated with multiplying summation of motor evoke potentials on the map (mV) by the area of the map (mm2) with the unit of mV*mm2
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Before 30-minute computer typing task
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Neurophysiological measures - Center of gravity of cortical mapping
Time Frame: Before 30-minute computer typing task
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Center of gravity of cortical mapping will be described in a x-y coordinate system (mm).
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Before 30-minute computer typing task
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Neurophysiological measures - Area of cortical mapping
Time Frame: Change from baseline area of cortical mapping after 30-minute rest (pilot subjects)
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Area of cortical mapping will be described with square millimeter (mm2)
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Change from baseline area of cortical mapping after 30-minute rest (pilot subjects)
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Neurophysiological measures - Volume of cortical mapping
Time Frame: Change from baseline volume of cortical mapping after 30-minute rest (pilot subjects)
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Volume of cortical mapping will be calculated with multiplying summation of motor evoke potentials on the map (mV) by the area of the map (mm2) with the unit of mV*mm2
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Change from baseline volume of cortical mapping after 30-minute rest (pilot subjects)
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Neurophysiological measures - Center of gravity of cortical mapping
Time Frame: Change from baseline center of gravity of cortical mapping of cortical mapping after 30-minute rest (pilot subjects)
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Center of gravity of cortical mapping will be described in a x-y coordinate system (mm).
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Change from baseline center of gravity of cortical mapping of cortical mapping after 30-minute rest (pilot subjects)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Scapular kinematics during arm elevation
Time Frame: Before 30-minute computer typing task
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Scapular kinematics, including anterior/posterior tilt, upward/downward rotation, and internal/external rotation in scapula plane elevation at 30°, 60°, 90°, and 120°, and will be described with degree (°).
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Before 30-minute computer typing task
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Scapular kinematics during performing the computer task
Time Frame: Change from baseline during the 30-minute computer typing task at 5, 10, 15, 20, 25, 30 minutes of the task
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The average of scapular kinematics, including anterior/posterior tilt, upward/downward rotation, and internal/external rotation will be calculated with a window of 10 seconds and will be described with degree (°).
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Change from baseline during the 30-minute computer typing task at 5, 10, 15, 20, 25, 30 minutes of the task
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Scapular muscles activation during arm elevation
Time Frame: Before 30-minute computer typing task
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The root mean square of electromyography (EMG) data of the upper trapezius, lower trapezius, and serratus anterior will be normalized by the maximum voluntary contraction amplitude (percentage of maximal voluntary contraction, %) and calculated over three 30° increments of motion during arm elevation from 30° to 120°, including 30° - 60°, 60° - 90°, and 90° - 120°.
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Before 30-minute computer typing task
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Scapular muscles activation during performing the computer task
Time Frame: Change from baseline during the 30-minute computer typing task at 5, 10, 15, 20, 25, 30 minutes of the task
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The root mean square of electromyography (EMG) data of the upper trapezius, lower trapezius, and serratus anterior will be calculated with a window of 10 seconds and will be normalized by the maximum voluntary contraction amplitude (percentage of maximal voluntary contraction, %).
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Change from baseline during the 30-minute computer typing task at 5, 10, 15, 20, 25, 30 minutes of the task
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Craniovertebral angle
Time Frame: Before 30-minute computer typing task
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Craniovertebral angle will be measured as the included angle between the tragus, C7 spinous process and the horizontal line and will be described with degree (°)
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Before 30-minute computer typing task
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Craniovertebral angle
Time Frame: Change from baseline during the 30-minute computer typing task at 5, 10, 15, 20, 25, 30 minutes of the task
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Craniovertebral angle will be measured as the included angle between the tragus, C7 spinous process and the horizontal line and will be described with degree (°)
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Change from baseline during the 30-minute computer typing task at 5, 10, 15, 20, 25, 30 minutes of the task
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Scapular kinematics during arm elevation
Time Frame: Change from baseline scapular kinematics after 30-minute rest (pilot subjects)
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Scapular kinematics, including anterior/posterior tilt, upward/downward rotation, and internal/external rotation in scapula plane elevation at 30°, 60°, 90°, and 120°, and will be described with degree (°).
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Change from baseline scapular kinematics after 30-minute rest (pilot subjects)
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Scapular muscles activation during arm elevation
Time Frame: Change from baseline scapular muscles activation after 30-minute rest (pilot subjects)
|
The root mean square of electromyography (EMG) data of the upper trapezius, lower trapezius, and serratus anterior will be normalized by the maximum voluntary contraction amplitude (percentage of maximal voluntary contraction, %) and calculated over three 30° increments of motion during arm elevation from 30° to 120°, including 30° - 60°, 60° - 90°, and 90° - 120°.
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Change from baseline scapular muscles activation after 30-minute rest (pilot subjects)
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Craniovertebral angle
Time Frame: Change from baseline craniovertebral angle after 30-minute rest (pilot subjects)
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Craniovertebral angle will be measured as the included angle between the tragus, C7 spinous process and the horizontal line and will be described with degree (°)
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Change from baseline craniovertebral angle after 30-minute rest (pilot subjects)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yin-Liang Lin, PhD, National Yang Ming University
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)
December 21, 2021
Primary Completion (Actual)
May 13, 2022
Study Completion (Actual)
May 13, 2022
Study Registration Dates
First Submitted
July 18, 2021
First Submitted That Met QC Criteria
August 10, 2021
First Posted (Actual)
August 11, 2021
Study Record Updates
Last Update Posted (Actual)
September 21, 2022
Last Update Submitted That Met QC Criteria
September 18, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- YM110059F
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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