The Effects of Kinesio Taping on Heel-Rise Endurance and Gastrocnemius Muscle Oxygenation in Healthy Young Adults

March 6, 2026 updated by: Muhammed Şeref Yıldırım, Trakya University

Acute Effects of Kinesio Taping on Heel-Rise Endurance and Gastrocnemius Muscle Oxygenation: A Randomized Controlled Crossover Trial

acilitative kinesio taping (KT) is commonly used by athletes to support muscle performance and delay fatigue. However, evidence regarding its effects on muscle endurance and oxygenation remains inconsistent. This study aims to investigate the acute effects of facilitative KT applied to the gastrocnemius muscle on heel-rise endurance performance and local muscle oxygenation in healthy young adults.

In this randomized crossover trial, participants will complete two experimental sessions: one with facilitative kinesio taping and one with sham taping. After taping application, participants will perform a single-leg heel-rise test to task failure. Muscle oxygenation will be continuously monitored using a portable near-infrared spectroscopy device. The findings of this study may contribute to understanding whether kinesio taping has immediate physiological and performance-related effects on calf muscle endurance.

Study Overview

Status

Not yet recruiting

Study Type

Interventional

Enrollment (Estimated)

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 Contact

Study Locations

    • Edirne
      • Edirne, Edirne, Turkey (Türkiye), 22100
        • Trakya 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:

  • Young adults aged 18-25 years
  • Cumberland Ankle Instability Tool score of ≥28

Exclusion Criteria:

  • Sedentary (<150 min/week moderate or <75 min/week vigorous physical activity)
  • Elite athletes
  • History of ankle sprain
  • Lower extremity fracture
  • Surgical intervention
  • Neurological or vestibular disorders

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Facilitative Kinesio Taping
Participants will receive facilitative kinesio taping applied to the gastrocnemius muscle using a Y-shaped elastic tape with approximately 50% stretch. After application, participants will perform a single-leg heel-rise test to task failure.
Y-shaped Kinesio Tex elastic tape applied to the gastrocnemius muscle with approximately 50% stretch following muscle facilitation principles.
Sham Comparator: Sham Taping
Participants will receive sham taping applied to the gastrocnemius muscle using a Y-shaped non-elastic tape without stretch. After application, participants will perform a single-leg heel-rise test to task failure.
Y-shaped Hypafix tape applied to the gastrocnemius muscle without stretch using the same anatomical configuration.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total Concentric Work (J)
Time Frame: Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Total concentric (positive) mechanical work (Joules) performed during a metronome-guided single-leg heel-rise test to task failure on the dominant limb. Work output will be measured using the Calf Raise App (computer-vision-based motion analysis).
Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Percent Change in Gastrocnemius Muscle Oxygen Saturation at 20 Seconds (%ΔSmO₂_20s)
Time Frame: From baseline rest to 20 seconds during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
From baseline rest to 20 seconds during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total number of single-leg heel-rise repetitions
Time Frame: Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Peak Heel-Rise Height (cm)
Time Frame: Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Maximum heel-rise height (cm) achieved during the single-leg heel-rise test, measured using the Calf Raise App.
Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Concentric Power (W)
Time Frame: Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Mean concentric power output (Watts) generated during the single-leg heel-rise test, measured using the Calf Raise App.
Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
End-Exercise Muscle Oxygen Saturation (SmO₂_end)
Time Frame: Measured at task failure during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Muscle oxygen saturation (SmO₂) value recorded at the point of task failure during the heel-rise test.
Measured at task failure during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Half-Recovery Time (HRT) of SmO₂
Time Frame: Measured during the 4-minute post-exercise recovery period following the heel-rise test in each experimental session (Day 1 and Day 2)
Time (seconds) required for muscle oxygen saturation (SmO₂) to recover to 50% of the difference between end-exercise SmO₂ and peak recovery SmO₂ during the standardized 4-minute recovery period.
Measured during the 4-minute post-exercise recovery period following the heel-rise test in each experimental session (Day 1 and Day 2)
Percent Change in Total Hemoglobin at 20 Seconds (%ΔtHb_20s)
Time Frame: From baseline rest to 20 seconds during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Percentage change in total hemoglobin (tHb) at 20 seconds of the heel-rise test relative to baseline (tHb_rest), measured using near-infrared spectroscopy.
From baseline rest to 20 seconds during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Eccentric Work (J) During Single-Leg Heel-Rise Test
Time Frame: Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)
Total eccentric (negative) mechanical work (Joules) performed during the metronome-guided single-leg heel-rise test to task failure on the dominant limb, measured using the Calf Raise App.
Measured during the single-leg heel-rise test in each experimental session (Day 1 and Day 2)

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 (Estimated)

April 1, 2026

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

October 1, 2026

Study Registration Dates

First Submitted

February 23, 2026

First Submitted That Met QC Criteria

March 6, 2026

First Posted (Actual)

March 11, 2026

Study Record Updates

Last Update Posted (Actual)

March 11, 2026

Last Update Submitted That Met QC Criteria

March 6, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • TU-FTR-MŞY-004

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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