- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05454449
Effect of Dynamic Taping on Landing Biomechanical Characteristics in Volleyball and Basketball Players With Symptoms of Patellar Tendinopathy
Study Overview
Status
Conditions
Detailed Description
Background: Patellar tendinopathy is an overuse injury associated with loading activities, and it is thought to be caused by repetitive force applied to the patellar tendon. Patellar tendinopathy is popular among basketball and volleyball players, particularly in men. Although altered biomechanical characteristics during landing has been suggested as one of the risk factors for the development of patellar tendinopathy, previous evidence failed to show the link between the sagittal plane biomechanics of the hip and knee joint and patellar tendinopathy; and little was known about the frontal and horizontal plane biomechanics in athletes with patellar tendinopathy. Among those factors contributing to the biomechanical characteristics, hip and quadriceps strength were shown linked with the presence of patellar tendinopathy, while other factors such as motor control or muscle activation have not been explored fully. The purpose of this study is to compare hip motor control and biomechanical characteristics of the hip and knee joint during landing in athletes with and without symptomatic patellar tendinopathy. The investigators hypothesize that the athletes with symptomatic patellar tendinopathy have poorer motor control and different landing biomechanics as compared with asymptomatic athletes.
Method: the investigators plan to recruit seventeen symptomatic patellar tendinopathy athletes for the experimental group, using demographic data (sex, age, height, weight, exercise type) of experimental group to match seventeen non-symptomatic athletes as control group. The assessment included hip motor control in various directions, and measurement of kinetics, kinematics and muscle activation during the step-down task, drop vertical jump and countermovement jump using the computer-aided video motion analysis system (Vicon) and the surface EMG (Delsys). The group difference will be tested using Mann-Whitney U test for the score of motor control test battery, and MANOVA for the biomechanical characteristics. The significant level was set at 0.05.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: Yi-Fen Shih, Ph.D
- Phone Number: +886-2-28267340
- Email: yfshih@nycu.edu.tw
Study Contact Backup
- Name: Chia-Yu Chen, B.S.
- Phone Number: +886-922117406
- Email: jolin151515878787@gmail.com
Study Locations
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Taipei, Taiwan, 11221
- National Yang-Ming Chiao-Tung University
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Contact:
- Yi-Fen Shih, Ph.D
- Phone Number: +886-2-28267340
- Email: yfshih@nycu.edu.tw
-
Contact:
- Chia-Yu Chen, B.S.
- Phone Number: +886-922117406
- Email: jolin151515878787@gmail.com
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
- 18 to 40 years old volleyball and basketball players
- Volleyball and basketball players with more than 2 years' training experience
- Volleyball and basketball players train over 90 minutes per week
Description
Inclusion Criteria:
- at the age of 18 to 40 years old
- volleyball and basketball players have more than 2 years training experience
- over 90 minutes of training time per week symptomatic group:
- having patellar tendon pain during loading task last for 3 months
- VISA-P questionnaire score ≦80 asymptomatic group:
- without any lower extremity pain in past 3 months
- VISA-P questionnaire score >80
Exclusion Criteria:
- volleyball and basketball players joined the school team or professional level
- unbearable pain occurred at the patellar tendon when conducting landing tasks
- with a history of patellar tendon pain before
- there are currently other acute injuries to the lower extremity
- lower extremity has undergone surgery or fracture in the past
- with a history of rheumatoid arthritis, systematic and neurological diseases
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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symptomatic group
Individuals with patellar tendon pain last for 3 months Individuals age between 18-40 years old Victorian Institute of Sport Assessment (VISA) Questionnaire score ≦80
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asymptomatic group
Individuals without any lower extremity pain in past 3 months Individuals age between 18-40 years old Victorian Institute of Sport Assessment (VISA) Questionnaire score >80
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
lower extremities joint angle
Time Frame: Immediately during the experiment
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hip joint flexion, extension, abduction, adduction, internal rotation, external rotation angle, knee joint flexion, extension angle
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Immediately during the experiment
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lower extremities joint angular velocity
Time Frame: Immediately during the experiment
|
hip joint flexion, extension, abduction, adduction, internal rotation, external rotation angle, knee joint flexion, extension angle divided by time
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Immediately during the experiment
|
lower extremities joint angular acceleration
Time Frame: Immediately during the experiment
|
lower extremities joint angular velocity divided by time
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Immediately during the experiment
|
ground reaction force
Time Frame: Immediately during the experiment
|
anterior, posterior, medial, lateral, vertical ground reaction force
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Immediately during the experiment
|
lower extremities joint force
Time Frame: Immediately during the experiment
|
calculate the reaction force between segments
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Immediately during the experiment
|
lower extremities joint moment
Time Frame: Immediately during the experiment
|
calculate the reaction moment between segments
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Immediately during the experiment
|
lower extremities joint power
Time Frame: Immediately during the experiment
|
calculate the reaction moment between segments
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Immediately during the experiment
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time to peak ground reaction force
Time Frame: Immediately during the experiment
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time period from initial contact to peak vertical ground reaction force
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Immediately during the experiment
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loading rate of ground reaction force
Time Frame: Immediately during the experiment
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peak vertical ground reaction force divided by time to peak ground reaction force
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Immediately during the experiment
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net joint work
Time Frame: Immediately during the experiment
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integral of joint power over time
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Immediately during the experiment
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patellar tendon force
Time Frame: Immediately during the experiment
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knee joint moment divided by moment arm
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Immediately during the experiment
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Lower extremity muscles activation during landing task
Time Frame: Immediately during the experiment
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The investigator will place surface electromyography (sEMG)(Delsys, USA) on subjects' bilateral gluteus maximum, gluteus medius, semitendinosus, biceps femoris, vastus medialis, vastus lateralis muscles to record muscles activities.
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Immediately during the experiment
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Hip joint motor control
Time Frame: pre-experiment
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The investigator will ask subject to do the hip flexion, hip internal rotation, hip abduction/external rotation and hip adduction control task.
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pre-experiment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Lower extremities joint angle
Time Frame: pre-experiment
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Measuring bilateral ankle dorsiflexion range of motion by the physical therapist with goniometer.
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pre-experiment
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Lower extremities muscle force
Time Frame: pre-experiment
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The hip extensor, external rotator, abductor, knee extensor, flexor muscle force measured by the physical therapist with a hand-held dynamometer
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pre-experiment
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Yi-Fen Shih, Ph.D, Department of Physical Therapy and Assistive Technology, National Yang-Ming Chiao-Tung University
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- YM109067F(2)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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