- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05757375
Mulligan Ankle Taping on Volleyball Players
August 20, 2025 updated by: Özge Ecem Şenel, Istinye University
Effects of Mulligan Ankle Taping in Volleyball Players With or Without Chronic Ankle Instability
34 volunteer professional volleyball players with (n=12) and without (n=22) CAI will include in the study.
Mulligan ankle taping will apply.
Measurements will take before and after the intervention.
Muscle tone, stiffness, and elasticity will measure with MyotonPRO hand-held device.
The static balance will measure with single leg stance test(SLST) while the eyes-closed, dynamic balance will measure with the Y balance test(YBT).
Single leg hopping test(SLHT) will evaluate performance and an active position sense test will use for JPS.
During the static and dynamic balance and performance tests, the ankle's confidence will be evaluated with the Visual Analog Scale (VAS).
The study aimed to determine the effect of Mulligan fibular taping over the Tibialis Anterior(TA), Peroneus Longus(PL), Gastrocnemius Lateralis(GCL), and Medialis(GCM) muscles on muscle tone, stiffness, elasticity, as well as the performance, joint position sense(JPS), static and dynamic balance in female volleyball players with and without chronic ankle instability(CAI).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
34
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
-
-
Zeytinburnu
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Istanbul, Zeytinburnu, Turkey, 34010
- Istinye 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
15 years to 24 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being between the ages of 15-24,
- Being a professional volleyball player,
- Training for 90 minutes at least 3 days a week,
- Turkish native speakers,
- For participants with chronic ankle instability, those with a Foot and Ankle Disability Index score below 90% and a Foot and Ankle Disability Index-Sport survey score below 75% were included.
Exclusion Criteria:
- An ankle sprain history in the last 6 weeks,
- Having a previous history of fracture in the lower extremity,
- Having bilateral chronic ankle instability,
- Pregnant athletes were excluded from the study.
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Volleyball players with Chronic Ankle Instability
Before the taping application, the application area of all athletes will be shaved.
It will be cleaned with an alcohol wipe before the application so that situations such as sweat or moisture do not reduce the effect of the banding.
For taping, while the athlete lies in a supine position on a portable stretcher, the leg weight will be taken by placing the athlete's foot on the abdomen with slight knee and hip flexion.
The rigid tape will be measured and cut obliquely starting approximately 2 cm anterior to the fibula and approximately 1 cm anterior to the lateral malleolus and ending in the middle of the anterior tibia region.
To increase the strength of the banding, another band will be added to it.
In the application, only banding will be preferred and mobilization will not be done.
|
Mulligan ankle taping is a noninvasive, painless, low-cost, and easily applicable technique of the Mulligan manual therapy concept.
It is frequently used in cases of ankle instability.
In healthy people, it is a method to prevent ankle sprains.
|
|
Experimental: Volleybal players without Chronic Ankle Instability
Before the taping application, the application area of all athletes will be shaved.
It will be cleaned with an alcohol wipe before the application so that situations such as sweat or moisture do not reduce the effect of the banding.
For taping, while the athlete lies in a supine position on a portable stretcher, the leg weight will be taken by placing the athlete's foot on the abdomen with slight knee and hip flexion.
The rigid tape will be measured and cut obliquely starting approximately 2 cm anterior to the fibula and approximately 1 cm anterior to the lateral malleolus and ending in the middle of the anterior tibia region.
To increase the strength of the banding, another band will be added to it.
In the application, only banding will be preferred and mobilization will not be done.
|
Mulligan ankle taping is a noninvasive, painless, low-cost, and easily applicable technique of the Mulligan manual therapy concept.
It is frequently used in cases of ankle instability.
In healthy people, it is a method to prevent ankle sprains.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Myotonometric Measurement
Time Frame: 4 weeks
|
MyotonPRO is a wireless handheld device that objectively evaluates the viscoelastic properties of muscles such as tone, stiffness, and elasticity with numerical values.
It creates a mechanical effect on the subcutaneous tissue and senses the response of the tissue.
The 3-millimeter probe of the device is placed 90 degrees perpendicular to the subcutaneous tissue to be measured.
With the measurement, muscle tone, stiffness, and elasticity are listed numerically.
Muscle tone will be calculated in hz and muscle stiffness in N/m.
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Single Leg Stand Test with Eyes Closed
Time Frame: 4 weeks
|
This test, which is used to evaluate the static balance ability, is applied with bare feet on a hard and flat surface.
During the test, participants are asked to close their eyes, place both hands on the opposite shoulder, and pull the untested leg to the abdomen with a 90-degree flexion angle from the hip and knee.
During the test, both legs should maintain this position without touching each other.
The test is started as soon as the participant's untested foot is not in contact with the ground, and is terminated when it touches the ground.
The test is repeated three times for both the right and left legs and the best result is referenced.
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4 weeks
|
|
Y Balance Test
Time Frame: 4 weeks
|
It is a reported dynamic test with good reliability requiring strength, flexibility, and proprioception.
It is a dynamic balance criterion applied to athletes and physically active people.
This measurement requires a setup first.
Three equal-length tapes adhere to the floor with 90°, 135°, and 135° angles between them, and a Y shape is obtained.
The directions to be tested are anterior, posterolateral, and posteromedial.
It is a highly reliable test to determine the risk of CABI and lower extremity injury.
|
4 weeks
|
|
Single Leg Hop Test
Time Frame: 4 weeks
|
It is a functional performance test.
This measurement requires a setup first.
The 3-meter tape is placed on the floor.
The athlete is asked to jump as far as possible and stay on one leg in the band.
The test is invalidated when the participant touches the floor with their untested foot or takes a few more small jumps to maintain their balance after the jump.
The distance from the starting level of the band to the heel contact at the end of the jump is measured.
This test is repeated 3 times until a successful jump is achieved and the best result is included in the evaluation.
|
4 weeks
|
|
Joint Position Test
Time Frame: 4 weeks
|
Joint position sense is the ability of the athlete to perceive the joint angle and repeat the same joint angle even if the extremity position changes.
The active position sense test is frequently used, especially in the clinic, due to its easy application.
While the test athlete's eyes are closed, he/she sits in such a way that the hip flexion angle of 90° and the knee flexion angle of 120° is achieved and the sole is in full contact with the ground.
The difference between the right and left dorsiflexion angles is measured with a smartphone from the goniometer application.
Dorsiflexion measurement is made by following the midline of the 5th metatarsal bone with a goniometer placed in the lateral malleolus.
The athlete's ankle to be tested is passively brought to 10° dorsiflexion and returned to the starting point.
Afterward, the athlete is asked to actively bring his ankle to the same angle.
The test is repeated three times for both ankles.
By subtracting the angle made by the athlete
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4 weeks
|
|
Confidence in the Ankle
Time Frame: 4 weeks
|
In order to evaluate the confidence of the athletes in the balance and performance tests, they are asked to score the confidence ratios before and after the intervention with the Visual Analogue Scale.
The VAS assessment is performed for the blindfolded one-leg stance test, the Y-star balance test (anterior, posteromedial, and posterolateral aspects), and the one-leg hop tests.
In order not to mislead the individual, each participant was asked, "How much was your confidence in your ankle during the test?" for each parameter.
the question is asked.
He is asked to show his confidence in the ankle on a 10 cm line and the distance is measured.
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: ÖZGE ECEM E ŞENEL, PT, Istinye 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)
January 22, 2023
Primary Completion (Actual)
May 12, 2023
Study Completion (Actual)
May 20, 2023
Study Registration Dates
First Submitted
January 12, 2023
First Submitted That Met QC Criteria
March 3, 2023
First Posted (Actual)
March 7, 2023
Study Record Updates
Last Update Posted (Actual)
August 21, 2025
Last Update Submitted That Met QC Criteria
August 20, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 10840098
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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