- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06942585
Effects of Dynamic and Kinesiology Taping on Balance and Kinesthesia in Healthy Adults (DAKTIK)
Acute Effects of Dynamic and Kinesiology Taping on Balance and Kinesthesia of the Lower Limbs in Healthy Adults
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Taping techniques are commonly used in rehabilitation and sports settings to support joint function, reduce pain, and improve proprioception. Dynamic tape (DT) and kinesiology tape (KT) differ in their mechanical properties and proposed mechanisms of action. While KT is elastic and mimics the properties of skin, DT offers higher elasticity and resistance, potentially providing enhanced mechanical support and proprioceptive feedback.
Although several studies have explored the effects of taping on balance and proprioception, direct comparisons between DT and KT, particularly when applied to both the ankle and knee joints, remain limited. This study seeks to address this gap by examining and comparing the immediate effects of DT and KT on static balance and kinesthesia of the lower limbs in healthy adults.
The findings may contribute to a better understanding of the clinical relevance of different taping methods and inform decision-making in preventive and therapeutic interventions targeting lower limb stability and proprioception.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Izola, Slovenia, 6310
- University of Primorska, Faculty of Health Sciences, Izola
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy adults aged 18-30 years
- No current pain or injury affecting the lower limbs
- Willingness to participate and provide informed consent
- No known allergy or sensitivity to adhesive materials
Exclusion Criteria:
- History of ankle sprain or anterior cruciate ligament (ACL) injury
- Any lower limb injury in the past 3 months
- Neurological or vestibular disorders affecting balance
- Skin conditions or wounds at the taping sites
- Participation in balance or proprioception training programs in the past month
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Kinesiology tape
Kinesiology tape (KT) applied to the knee and ankle
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An elastic therapeutic tape applied to the ankle and knee using standard kinesiology taping techniques.
The tape is stretched to approximately 10-15% during application and is designed to mimic the properties of human skin.
It aims to provide sensory stimulation, improve proprioceptive feedback, and support joint function without limiting range of motion.
The application targets muscles and tendons surrounding the knee and ankle, commonly used in both preventive and rehabilitative physiotherapy.
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Experimental: Dynamic tape
Dynamic tape (DT) applied to the knee and ankle
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A biomechanical tape characterized by high elasticity (over 200%) and strong resistance, applied to the ankle and knee to assist movement and absorb load.
The tape is applied in a shortened muscle position with maximal stretch across the joint, following the manufacturer's guidelines (GripIt ACTIVETAPE, 5 cm width).
This taping method aims to provide both mechanical support and neurosensory input, facilitating muscle activation and improving joint stability during movement.
It is used to address both biomechanical and proprioceptive components of lower limb control.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean Velocity of Center of Pressure During Single-Leg Stance [mm/s]
Time Frame: Immediately before and within 10 minutes after tape application (per condition)
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Mean velocity of the CoP will be measured during the 30-second single-leg stance using a force plate.
The outcome will be compared across the no tape, kinesiology tape, and dynamic tape conditions.
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Immediately before and within 10 minutes after tape application (per condition)
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Sway Amplitude of Center of Pressure During Single-Leg Stance [mm]
Time Frame: Immediately before and within 10 minutes after tape application (per condition)
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During the same 30-second single-leg stance test, the sway amplitude of the CoP will be recorded using a force plate.
This outcome will be used to evaluate changes in postural control across taping conditions.
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Immediately before and within 10 minutes after tape application (per condition)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee Joint Kinesthesia [°]
Time Frame: Immediately before and within 10 minutes after tape application (per condition)
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Kinesthesia will be assessed using a passive-to-active joint position reproduction test with a digital goniometer (EasyAngle).
Participants will attempt to replicate a reference knee flexion angle (45°) with eyes closed.
The absolute angular error (in degrees) between the target and reproduced position will be calculated.
Measurements will be compared across the no tape, kinesiology tape, and dynamic tape conditions to evaluate the acute effects of taping on proprioceptive accuracy.
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Immediately before and within 10 minutes after tape application (per condition)
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Collaborators and Investigators
Sponsor
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
Other Study ID Numbers
- DAKTIK
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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