- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06580925
Effects of Dynamic Taping on Shoulder Isokinetics Strength and Muscle Fatigue.
May 19, 2025 updated by: Yin-Liang Lin, National Yang Ming Chiao Tung University
Effects of Dynamic Taping on Shoulder Strength, Fatigue, Corticomotor Control and Neuromuscular Control
Maintaining shoulder stability requires good neuromuscular control.
Imbalances in shoulder internal and external rotator strength may increase the risk of shoulder injuries in overhead athletes, and the compromised fatigue resistance of the external rotators may worsen this imbalance during sports activities.
Additionally, poor scapular neuromuscular control is associated with shoulder problems, such as shoulder impingement syndrome.
Previous research has shown that individuals with shoulder impingement syndrome exhibit poor scapular motion control and altered corticomotor control.
Poor scapular motion control, pain, functional impairment, and changes in corticomotor control interact to form a vicious cycle.
Various treatments have been attempted to improve neuromuscular control, including taping.
Most past studies have focused on the efficacy of rigid tape and kinesio tape, while dynamic tape has gained popularity in recent years.
Due to its material properties, dynamic tape is theoretically able to absorb loads, provide force, and correct movements.
However, there is currently a lack of evidence supporting the effectiveness of dynamic tape.
No research has yet explored whether dynamic tape can provide force to increase muscle strength and reduce fatigue or whether its movement correction functions can improve neuromuscular control and corticomotor control.
Therefore, this project plans to conduct an experiment to investigate the effects of dynamic tape on external rotator strength and fatigue in recreational overhead athletes, as well as its impact on neuromuscular control and corticomotor excitability in recreational overhead athletes with shoulder impingement syndrome.
In the experiment, 37 healthy recreational overhead athletes will participate in three testing sessions spaced one week apart, receiving kinesio tape, dynamic tape, and sham tape.
After taping, they will perform fatigue-inducing activities.
Isokinetic strength of internal and external rotators will be measured before taping, after taping, and after fatigue-inducing activities to observe the effects of dynamic tape on muscle strength and fatigue compared to kinesio tape and sham tape.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
37
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 city
-
Taipei, Taipei city, Taiwan, 112
- National Yang Ming Chiao Tung 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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- practice overhead exercise more than six hours a week
- aged 18 to 40 years old
Exclusion Criteria:
- have a history of dislocation, fracture, or surgery of neck or upper extremity
- a history of pain or injuries over the neck or upper extremities within the past 12 months
- brain injury and neurological impairment
- arm elevation angle is less than 150 degrees
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: Treatment
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Sham Comparator: sham tape
|
sham
|
|
Active Comparator: kinesio tape
|
Kinesio taping will be applied to correct shoulder posture and facilitate shoulder external rotators
|
|
Experimental: dynamic tape
|
Dynamic tape will be applied to correct shoulder alignment and assist concentric contraction and eccentric control of external rotators
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shoulder isokinetic muscle strength
Time Frame: Change from baseline shoulder isokinetic muscle strength after application of taping (about 4 minutes) and execution of a fatigue protocol (about 5 minutes)
|
Shoulder isokinetic internal and external muscle strength will be measured by dynamometer in 2 modes (concentric/concentric, concentric/eccentric) at 2 angular velocities (60°/s & 240°/s), 1 set of 5 repetitions for each angular velocities.
Shoulder isokinetic muscle strength will be normalized by body weight (BW) and described with peak torque/BW (N·m·kg-1).
|
Change from baseline shoulder isokinetic muscle strength after application of taping (about 4 minutes) and execution of a fatigue protocol (about 5 minutes)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Median frequency
Time Frame: Change from baseline shoulder isokinetic muscle strength after execution of a fatigue protocol (about 5 minutes)
|
The median frequency calculated from electromyographic data of shoulder internal and external rotators.
The percentage change in median frequency will be calculated and will be described with percentage (%)
|
Change from baseline shoulder isokinetic muscle strength after execution of a fatigue protocol (about 5 minutes)
|
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)
March 24, 2024
Primary Completion (Actual)
September 1, 2024
Study Completion (Estimated)
June 30, 2025
Study Registration Dates
First Submitted
August 27, 2024
First Submitted That Met QC Criteria
August 28, 2024
First Posted (Actual)
August 30, 2024
Study Record Updates
Last Update Posted (Actual)
May 21, 2025
Last Update Submitted That Met QC Criteria
May 19, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NYCU112007AF-1
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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