Rate of EMG Rise and Rate of Force Development of Scapular Muscles

June 17, 2022 updated by: National Taiwan University Hospital

Rate of EMG Rise and Rate of Force Development of Scapular Muscles in Overhead Athletes With Different Types of Scapular Dyskinesis

The investigators will clarify rate of electromyography (EMG) rise and rate of force development in overhead athletes on scapular muscles, including upper trapezius, lower trapezius and serratus anterior. The correlation between rate of EMG rise and rate of force development will also be examined.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

The contributing factor of scapular dyskinesis can be bony and joint-related issues, neurologic problems, soft tissue problems. Patient with thoracic kyphosis, pectoralis minor stiffness, long thoracic nerve injury, and so on can lead to scapular dyskinesis and further shoulder dysfunction. During shoulder movement, the neuromuscular control of the scapular muscles also play an important role. Previous studies found that participants with pattern 1 and 2 scapular dyskinesis had lesser lower trapezius (5%, P =.025) and serratus anterior activity (10%, P =.004), and higher upper trapezius activity (14%, P =.01) in pattern 2 participants during arm lowering compared to normal participants. Furthermore, the intervention focus on neuromuscular control can change the recruitment pattern of participants with scapular dyskinesis. Significant increases in activation of the middle and lower trapezius (MT: 4.9 ± 2.4% of the maximal voluntary isometric contraction (MVIC); LT: 10.2 ± 6.8% MVIC, p < 0.0 25) were found with conscious control in 3 exercises among the 3 dyskinesis groups, and increased serratus anterior activation (11.2 ± 4.8% MVIC, p < 0.0 25) was found in the concentric phase of side-lying external rotation in the pattern 1 and 1 + 2 groups. The studies show that the muscle recruitment is highly related to the scapular dyskinesis.

However, there are some limitation in the previous studies which presented the outcome by EMG amplitude. First, no matter with or without intervention, previous studies fail to show difference between groups in some condition. Although, there are some difference in lowering phase, the results fail to show difference in elevation phase and some degree of lowering phase. Second, substantial cancellation of the EMG interference signal can occur. The positive and negative signal will be offset. Last, not only neural effect but also contractile effect will be captured. Contraction type, including concentric, eccentric or isometric, will occur in a movement, so the signal will be affected. As the result, another method to represent neuromuscular effect should be considered.

The rate of EMG rise (RER; Formula: ΔEMG/Δtime) has been used to evaluate the rate of muscle activation in order to account for the neural factors that contribute to rate of force development (RFD; Formula: Δforce/Δtime). The onset (<75 ms) of a rapid contraction indicates a role for neural factors. Previous studies with RER outcome have been conducted to see the effect of pain, aging or training. It has been reported that RER reduce with pain and aging while increase after training, and better sensitivity to distinguish difference than peak EMG amplitude (PEMG). The significant difference is found in both upper trapezius and deltoid for RER but only in upper trapezius for PEMG. However, most of the studies about RER are conducted on lower extremity or female worker and no study conducted on athletes, not to mention athletes with scapular dyskinesis.

The overhead sports are characterized with forced and rapid movement. The more sensitive and functional measurement of RER may detect the difference of overhead athletes with different type scapular dyskinesis. Therefore, the purposes of this study are to compare the RER, PEMG, RFD and peak force on scapular muscles (UT, LT, SA) among different types of scapular dyskinesis at 2 arm elevation angles (30, 90 degree). Additionally, to investigate the correlation between RER and RFD. The investigators hypothesize that overhead athletes with scapular dyskinesis will demonstrate significant lower RER and RFD, and there will be significant positive correlation between RER and RFD.

Study Type

Observational

Enrollment (Anticipated)

40

Contacts and Locations

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

Study Contact

Study Contact Backup

  • Name: Yi-Hsuan Weng, MS
  • Phone Number: 02-33668126

Study Locations

      • Taipei, Taiwan, 100
        • National Taiwan University Hospital

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

Sampling Method

Non-Probability Sample

Study Population

Scapular dyskinesis is defined as abnormal scapular position and motion. It can be divided in 4 patterns. It has been reported that overhead athletes have higher prevalence (61%) compare to non-overhead athletes (33%). Additionally, athletes with scapular dyskinesis have 43% greater risk of developing shoulder pain than those without scapular dyskinesis. Due to higher prevalence with greater injury risk, scapular dyskinesis plays the important role of injury process that need to be concerned for the overhead athletes.

Description

Inclusion Criteria:

  • Playing overhead sports for at least 1 year.
  • Still active in training or competition.
  • The frequency of training or game should be at least 2 times per week, 1 hour per time.

Exclusion Criteria:

  • Subjects with shoulder pain onset due to trauma, a history of shoulder fractures or dislocation, cervical radiculopathy, degenerative joint disease of the shoulder, surgical interventions on the shoulder, or inflammatory arthropathy.
  • Visual analog scale (VAS) > 5 during movement in the experiment.

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

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
type 1 scapular dyskinesis
type 1 scapular dyskinesis classified by dyskinesis classification test
rapid arm elevation to see the different of EMG rise and force development
type 2 scapular dyskinesis
type 2 scapular dyskinesis classified by dyskinesis classification test
rapid arm elevation to see the different of EMG rise and force development
type 3 scapular dyskinesis
type 3 scapular dyskinesis classified by dyskinesis classification test
rapid arm elevation to see the different of EMG rise and force development
type 4 scapular dyskinesis
type 4 scapular dyskinesis classified by dyskinesis classification test
rapid arm elevation to see the different of EMG rise and force development

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rate of EMG rise
Time Frame: Baseline
Surface EMG electrodes (The Ludlow Company LP, Chocopee, MA) were placed after shaving and preparation with alcohol to decrease skin impedance (typically 10 kΩ or less). An impedance meter (Model F-EZM5, Astro-Med Inc., Ri, USA) will be used to measure impedance between the electrodes and skin over the muscle. Bipolar surface EMG electrodes with an interelectrode (center-to-center) distance of 20 mm will be placed upper trapezius, lower trapezius and serratus anterior of the dominant shoulder. Electrodes for upper trapezius were placed midway between acromion and the seventh spinous process of cervical vertebrae. The lower trapezius was palpated obliquely upward and laterally along the line between intersection of the spine of scapula and the seventh spinous process of thoracic vertebrae. Electrodes for serratus anterior was placed anterior to the latissimus dorsi and posterior to pectoralis major. The reference electrode was placed on the ipsilateral clavicle
Baseline
rate of force development
Time Frame: Baseline
The force-sensitive measurement system (FlexiForce ELFTM, New Taipei City, Taiwan, R.O.C.) will be used for force detection. It combines three single-point FlexiForce B201 sensors, one handle containing USB-interface electronics, and Windows-compatible software (Figure 2). Three circle sensors (diameter 9.53 mm; thickness 0.203 mm) are able to detect therange of force as low (4.4-111N), medium (111-667N) and, high level (667-4448N), respectively. This ensures that the various force during measurement can be measured by the appropriate sensor. When the sensor detects the force, the software will display the histogram, curve graph, or number of the force detected as the real-time bio-feedback. The sampling rate of the data collection is set at 200Hz.
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Posterior displacement of the scapula
Time Frame: Baseline
The modified scapulometer will be stationed at one side to measure the distance from the root of the spine (ROS) and the inferior angle (INF) of the scapula to the thoracic wall, respectively. Before conducting the test, two anatomic landmarks, ROS and INF, will be identified and marked. Then two parallel landmarks on the same level of the ROS and INF, approximately 1 cm medial to the scapular medial border, will be marked. The first rater slides the digital caliper anteriorly toward the parallel landmark until firm contact. Posterior displacement of the scapula will be recorded by the second rater based on the digital caliper.
Baseline

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jiu-Jenq Lin, PhD, National Taiwan University Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • 1. Kibler WB, Ludewig PM, McClure PW, Michener LA, Bak K, Sciascia AD. Clinical implications of scapular dyskinesis in shoulder injury: the 2013 consensus statement from the 'Scapular Summit'. Br J Sports Med 2013;47:877-85. 2. Huang TS, Huang HY, Wang TG, Tsai YS, Lin JJ. Comprehensive classification test of scapular dyskinesis: A reliability study. Manual therapy 2015;20:427-32. 3. McClure P, Tate AR, Kareha S, Irwin D, Zlupko E. A clinical method for identifying scapular dyskinesis, part 1: reliability. J Athl Train 2009;44:160-4. 4. Burn MB, McCulloch PC, Lintner DM, Liberman SR, Harris JD. Prevalence of Scapular Dyskinesis in Overhead and Nonoverhead Athletes: A Systematic Review. Orthopaedic journal of sports medicine 2016;4:2325967115627608. 5. Hickey D, Solvig V, Cavalheri V, Harrold M, McKenna L. Scapular dyskinesis increases the risk of future shoulder pain by 43% in asymptomatic athletes: a systematic review and meta-analysis. Br J Sports Med 2018;52:102-10. 6. Longo UG, Risi Ambrogioni L, Berton A, Candela V, Massaroni C, Carnevale A, et al. Scapular Dyskinesis: From Basic Science to Ultimate Treatment. Int J Environ Res Public Health 2020;17. 7. Huang TS, Ou HL, Huang CY, Lin JJ. Specific kinematics and associated muscle activation in individuals with scapular dyskinesis. Journal of shoulder and elbow surgery 2015;24:1227-34. 8. Ou HL, Huang TS, Chen YT, Chen WY, Chang YL, Lu TW, et al. Alterations of scapular kinematics and associated muscle activation specific to symptomatic dyskinesis type after conscious control. Manual therapy 2016;26:97-103. 9. Huang TS, Du WY, Wang TG, Tsai YS, Yang JL, Huang CY, et al. Progressive conscious control of scapular orientation with video feedback has improvement in muscle balance ratio in patients with scapular dyskinesis: a randomized controlled trial. Journal of shoulder and elbow surgery 2018;27:1407-14. 10. Lawrence JH, De Luca CJ. Myoelectric signal versus force relationship in different human muscles. Journal of applied physiology: respiratory, environmental and exercise physiology 1983;54:1653-9. 11. Jay K, Schraefel M, Andersen CH, Ebbesen FS, Christiansen DH, Skotte J, et al. Effect of brief daily resistance training on rapid force development in painful neck and shoulder muscles: randomized controlled trial. Clin Physiol Funct Imaging 2013;33:386-92. 12. Andersen LL, Andersen JL, Suetta C, Kjaer M, Søgaard K, Sjøgaard G. Effect of contrasting physical exercise interventions on rapid force capacity of chronically painful muscles. J Appl Physiol (1985) 2009;107:1413-9. 13. Andersen LL, Holtermann A, Jørgensen MB, Sjøgaard G. Rapid muscle activation and force capacity in conditions of chronic musculoskeletal pain. Clin Biomech (Bristol, Avon) 2008;23:1237-42. 14. Andersen LL, Nielsen PK, Søgaard K, Andersen CH, Skotte J, Sjøgaard G. Torque-EMG-velocity relationship in female workers with chronic neck muscle pain. Journal of biomechanics 2008;41:2029-35. 15. Weon JH, Kwon OY, Cynn HS, Lee WH, Kim TH, Yi CH. Real-time visual feedback can be used to activate scapular upward rotators in people with scapular winging: an experimental study. J Physiother 2011;57:101-7. 16. Alberta FG, ElAttrache NS, Bissell S, Mohr K, Browdy J, Yocum L, et al. The development and validation of a functional assessment tool for the upper extremity in the overhead athlete. The American journal of sports medicine 2010;38:903-11. 17. Oh JH, Kim JY, Limpisvasti O, Lee TQ, Song SH, Kwon KB. Cross-cultural adaptation, validity and reliability of the Korean version of the Kerlan-Jobe Orthopedic Clinic shoulder and elbow score. JSES open access 2017;1:39-44.

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 (Anticipated)

July 1, 2022

Primary Completion (Anticipated)

September 1, 2022

Study Completion (Anticipated)

December 31, 2022

Study Registration Dates

First Submitted

June 14, 2022

First Submitted That Met QC Criteria

June 14, 2022

First Posted (Actual)

June 21, 2022

Study Record Updates

Last Update Posted (Actual)

June 24, 2022

Last Update Submitted That Met QC Criteria

June 17, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

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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