- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07446283
Motion and EMG Analysis of the Forehand Topspin, Forehand Stroke, and Forehand Attack in Elite Table Tennis Players
Motion and Electromyographic Analysis of the Forehand Topspin Against Topspin, Forehand Topspin Against Backspin, Forehand Stroke, and Forehand Attack in Elite Table Tennis Players
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study participants will be elite table tennis players aged between 13 and 40. Participants must have competed in the Chinese Taipei Table Tennis Ranking Tournament or the National Table Tennis Championships within the past three years and have at least four years of table tennis experience, and train for more than 10 hours per week.
The study involves four types of forehand strokes: forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: YIN-LIANG LIN
- Phone Number: +886-2-28267288
- Email: yllin1020@nycu.edu.tw
Study Contact Backup
- Name: HSIU-LI LIN
- Email: bromine.be12@nycu.edu.tw
Study Locations
-
-
Taiwan
-
Taipei, Taiwan, Taiwan, 112
- Recruiting
- National Yang Ming Chiao Tung University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- The ages range from 13 to 40 years old
- Competed in the Chinese Taipei Table Tennis Ranking Tournament or the National Table Tennis Championships within the past three years
- At least four years of table tennis experience, and train for more than 10 hours per week
Exclusion Criteria:
- History of upper limb surgery or fracture
- History of shoulder dislocation
- History of spine injury in the last year
- Systemic autoimmune disease or cancer
- Pregnancy
- Any neurological complications
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
table tennis players (healthy group)
elite table tennis players without shoulder pain
|
forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack
|
|
table tennis players (shoulder pain group)
elite table tennis players with shoulder pain
|
forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trunk muscles activation during forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack
Time Frame: Immediately during the experiment
|
The root mean square of electromyography (EMG) data of bilateral erector spinae and bilateral abdominal external oblique will be normalized by the maximum voluntary contraction amplitude (percentage of maximal voluntary contraction, %)
|
Immediately during the experiment
|
|
Trunk kinematics during forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack
Time Frame: Immediately during the experiment
|
Trunk kinematics, including flexion, extension, lateral flexion and rotation, were measured in degrees (°) across four conditions: forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack.
|
Immediately during the experiment
|
|
Upper limbs muscles activation during forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack
Time Frame: Immediately during the experiment
|
The root mean square of electromyography (EMG) data of the biceps brachii, triceps brachii, anterior deltoid, and pectoralis Major will be normalized by the maximum voluntary contraction amplitude (percentage of maximal voluntary contraction, %) and calculated over forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack.
|
Immediately during the experiment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trunk mobility
Time Frame: Immediately during the experiment
|
Range of motion of the thoracolumbar spine, described with degrees (°).
|
Immediately during the experiment
|
|
Shoulder mobility
Time Frame: Immediately during the experiment
|
Range of motion of the glenohumeral joint, described with degrees (°).
|
Immediately during the experiment
|
|
Shoulder motor control
Time Frame: Immediately during the experiment
|
A clinical assessment of movement quality during shoulder flexion, abduction, external rotation, and internal rotation
|
Immediately during the experiment
|
|
Trunk motor control
Time Frame: Immediately during the experiment
|
A clinical assessment of movement quality during trunk rotation
|
Immediately during the experiment
|
|
Shoulder kinematics during forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack
Time Frame: Immediately during the experiment
|
Shoulder kinematics, including flexion, abduction, horizontal adduction and horizontal adduction, were measured in degrees (°) across four conditions: forehand topspin against topspin, forehand topspin against backspin, forehand stroke, and forehand attack.
|
Immediately during the experiment
|
|
Trunk muscle strength
Time Frame: Immediately during the experiment
|
Isometric muscle strength of the erector spinae and external oblique abdominal muscles will be evaluated using a hand-held dynamometer (MicroFET2).
Data will be expressed in newton (N).
|
Immediately during the experiment
|
|
Shoulder muscle strength
Time Frame: Immediately during the experiment
|
Isometric muscle strength of the biceps brachii, triceps brachii, anterior deltoid and pectoralis major muscles will be evaluated using a hand-held dynamometer (MicroFET2).
Data will be expressed in newton (N).
|
Immediately during the experiment
|
Collaborators and Investigators
Investigators
- Principal Investigator: YIN-LIANG LIN, National Yang Ming Chiao Tung University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NYCU114030AF
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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