Effects of Dynamic and Kinesiology Taping on Balance and Kinesthesia in Healthy Adults (DAKTIK)

May 19, 2025 updated by: Žiga Kozinc, University of Primorska

Acute Effects of Dynamic and Kinesiology Taping on Balance and Kinesthesia of the Lower Limbs in Healthy Adults

This study aims to investigate the acute effects of dynamic tape (DT) and kinesiology tape (KT) on balance and kinesthesia of the lower limbs in healthy young adults. Participants will undergo assessments of static balance and knee joint position sense before and after the application of each taping condition. The study seeks to determine whether DT or KT can provide immediate improvements in postural stability and proprioceptive accuracy.

Study Overview

Status

Completed

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

Interventional

Enrollment (Actual)

24

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

      • Izola, Slovenia, 6310
        • University of Primorska, Faculty of Health Sciences, Izola

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:

  • 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

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: 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
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.
Experimental: Dynamic tape
Dynamic tape (DT) applied to the knee and ankle
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.

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)
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.
Immediately before and within 10 minutes after tape application (per condition)
Sway Amplitude of Center of Pressure During Single-Leg Stance [mm]
Time Frame: Immediately before and within 10 minutes after tape application (per condition)
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.
Immediately before and within 10 minutes after tape application (per condition)

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)
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.
Immediately before and within 10 minutes after tape application (per condition)

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)

April 1, 2025

Primary Completion (Actual)

May 16, 2025

Study Completion (Actual)

May 19, 2025

Study Registration Dates

First Submitted

April 8, 2025

First Submitted That Met QC Criteria

April 16, 2025

First Posted (Actual)

April 24, 2025

Study Record Updates

Last Update Posted (Actual)

May 23, 2025

Last Update Submitted That Met QC Criteria

May 19, 2025

Last Verified

May 1, 2025

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)?

UNDECIDED

IPD Plan Description

Individual participant data (IPD) will not be shared due to the small sample size, the nature of the data (short-term, non-clinical outcomes), and to protect participant confidentiality. Aggregated results will be published in scientific outlets and shared upon request.

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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