- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07703930
Effects of Different Kinesio Taping Techniques on Plantar Fascia Stiffness, Balance, and Ankle Joint Position Sense in Healthy Young Adults (KT-PF)
The Effects of Different Kinesio Taping Techniques on Plantar Fascia Stiffness, Balance, and Ankle Joint Position Sense in Healthy Young Adults
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Kinesio taping is commonly used to improve neuromuscular control, proprioception, and lower-extremity biomechanics. However, the comparative effects of different kinesio taping techniques on plantar fascia mechanical behavior and functional performance remain unclear. This study was designed as a prospective randomized controlled trial to investigate the effects of facilitation kinesio taping, ankle stabilization taping, and sham taping on plantar fascia elasticity, dynamic balance, and ankle joint position sense.
A total of 120 healthy young adults between the ages of 18 and 25 years participated in the study. Participants were randomly allocated into three intervention groups. Group 1 received facilitation kinesio taping, Group 2 received ankle stabilization taping, and Group 3 received sham taping. Plantar fascia viscoelastic properties including frequency, stiffness, relaxation time, and creep were evaluated using the MyotonPRO device. Dynamic balance performance was assessed using the modified Star Excursion Balance Test (mSEBT), and ankle joint position sense was evaluated using the active angle reproduction method with the Dr.Goniometer application.
Measurements were performed at baseline, 24 hours, and 48 hours after tape application. The primary objective of the study was to determine whether different kinesio taping methods produce different short-term effects on plantar fascia elasticity and lower-extremity function.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Beylikduzu
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Istanbul, Beylikduzu, Turkey (Türkiye), 34520
- Istanbul Aydin University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy young adults aged 18-25 years
- No history of lower extremity injury affecting ankle function
- Full, pain-free ankle range of motion in all directions
Exclusion Criteria:
- History of ankle dislocation or fracture within the previous year
- Previous foot or ankle surgery
- Pain during ankle movements
- Open wounds or skin allergy preventing kinesio taping application
- Psychiatric disorders or cognitive impairment affecting participation
Study Plan
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: Facilitation KT Group
Participants received facilitation kinesio taping applied to the plantar fascia.
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Facilitation kinesio taping was applied to support plantar fascia function.
|
|
Experimental: Ankle Stabilization KT Group
Participants received ankle stabilization kinesio taping intervention.
|
Ankle stabilization taping was applied to improve ankle stability and proprioceptive control.
|
|
Sham Comparator: Sham Taping Group
Participants received sham taping without therapeutic tension or corrective technique.
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Sham taping was applied without therapeutic tension or corrective technique.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in plantar fascia frequency measured by MyotonPRO
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
Plantar fascia frequency will be assessed using the MyotonPRO device.
The measurement evaluates the oscillation frequency of the plantar fascia tissue following mechanical impulse application.
Measurements will be performed at baseline, 24 hours, and 48 hours after kinesio taping intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
|
Change in plantar fascia stiffness measured by MyotonPRO
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
Plantar fascia stiffness(N/m) will be assessed using the MyotonPRO device.
The measurement represents the resistance of plantar fascia tissue to external mechanical deformation.
Measurements will be performed at baseline, 24 hours, and 48 hours after kinesio taping intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
|
Change in plantar fascia decrement measured by MyotonPRO
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
Plantar fascia decrement will be assessed using the MyotonPRO device.
Decrement represents the mechanical damping characteristics and elasticity of the plantar fascia tissue.
Measurements will be performed at baseline, 24 hours after intervention, and 48 hours after intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
|
Change in plantar fascia relaxation time measured by MyotonPRO
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
Plantar fascia relaxation(ms) time will be assessed using the MyotonPRO device.
Relaxation time represents the time required for the tissue to return toward its baseline mechanical state after mechanical deformation.
Measurements will be performed at baseline, 24 hours, and 48 hours after kinesio taping intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
|
Change in plantar fascia creep measured by MyotonPRO
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
Plantar fascia creep(De) will be assessed using the MyotonPRO device.
Creep represents the gradual deformation behavior of plantar fascia tissue under mechanical loading.
Measurements will be performed at baseline, 24 hours, and 48 hours after kinesio taping intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in anterior reach distance measured by modified Star Excursion Balance Test
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
Dynamic balance performance will be assessed using the anterior reach direction of the modified Star Excursion Balance Test (mSEBT).
Reach distance will be normalized to limb length and reported as a percentage.
Measurements will be performed at baseline, 24 hours, and 48 hours after kinesio taping intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
|
Change in posteromedial reach distance measured by modified Star Excursion Balance Test
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
Dynamic balance performance will be assessed using the posteromedial reach direction of the modified Star Excursion Balance Test (mSEBT).
Reach distance will be normalized to limb length and reported as a percentage.
Measurements will be performed at baseline, 24 hours, and 48 hours after kinesio taping intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
|
Change in posterolateral reach distance measured by modified Star Excursion Balance Test
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
Dynamic balance performance will be assessed using the posterolateral reach direction of the modified Star Excursion Balance Test (mSEBT).
Reach distance will be normalized to limb length and reported as a percentage.
Measurements will be performed at baseline, 24 hours, and 48 hours after kinesio taping intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
|
Change in composite score of modified Star Excursion Balance Test
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
The composite score of dynamic balance performance will be calculated from anterior, posteromedial, and posterolateral reach distances obtained during the modified Star Excursion Balance Test.
The composite score will be normalized to limb length and reported as a percentage.
Measurements will be performed at baseline, 24 hours, and 48 hours after kinesio taping intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
|
Change in ankle joint position sense accuracy measured by active angle reproduction method
Time Frame: Baseline, 24 hours after intervention, and 48 hours after intervention
|
Ankle joint position sense will be assessed using the active angle reproduction method with the Dr.Goniometer application.
Participants will reproduce target ankle positions of 5 degrees plantar flexion and 5 degrees dorsiflexion.
The absolute difference between the target angle and reproduced angle will be recorded as angular error.
Measurements will be performed at baseline, 24 hours, and 48 hours after kinesio taping intervention.
|
Baseline, 24 hours after intervention, and 48 hours after intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Yasemin Şahbaz, Assistant Professor, PhD, Istanbul Beykent University
Publications and helpful links
General Publications
- Hosseini R. Effects of Different Kinesio Taping Methods on Plantar Fascia Elasticity, Balance, Vertical Jump Performance, Ankle Function, and Joint Position Sense. Master's Thesis. Istanbul Aydin University, Graduate Education Institute, Department of Physiotherapy and Rehabilitation, 2025.
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
- KT-PF-2025-IST-01
- IAU-ETHICS-116-2025 (Other Identifier: Istanbul Aydin University)
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
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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