- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07572201
The Effect of Kinesio Taping Applied to the Gastrocnemius Muscle on Muscle Oxygenation, Pain Pressure Threshold, and Muscle Mechanical Properties
April 29, 2026 updated by: Kübra Kendal, Okan University
Investigation of the Effects of Kinesio Taping Applied to the Gastrocnemius Muscle on Muscle Oxygenation, Pain Pressure Threshold, and Muscle Mechanical Properties in Young Healthy Individuals
The aim of this study is to investigate the effects of kinesio taping applied to the gastrocnemius muscle on muscle oxygenation, pain pressure threshold, and mechanical properties of the muscle in healthy young individuals.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Individuals meeting the inclusion criteria will be randomly assigned to two groups using block randomization: the Kinesio® tape group (KTG) and the placebo group (PG).
Following assessments, individuals will be assigned to their respective groups and will receive Kinesio® tape application from a physiotherapist.
Assessments will be repeated for all individuals at 1 hour and 36 hours after application.
Study Type
Interventional
Enrollment (Estimated)
50
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
- Name: Kubra Kendal
- Phone Number: +90 530-233-8078
- Email: kubra.kendal@okan.edu.tr
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:
- Right lower extremity being dominant,
- Not having suffered a musculoskeletal injury to the lower extremity in the last 3 months
Exclusion Criteria:
- Having any orthopedic, neurological, circulatory, or psychiatric diagnosis,
- Having a history of lower extremity surgery,
- Having an allergy to KT or similar tapes,
- Using muscle relaxants and non-steroidal anti-inflammatory drugs,
- Having received physiotherapy and rehabilitation treatment within the last 3 months.
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: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Kinesio® tape group (KT)
KT will be applied by a certified physiotherapist following standardized procedures.
The skin of the lower leg will be cleaned with alcohol before application.
Participants will be positioned prone with their lower extremities fully extended, knees in full extension, and ankles in a neutral position.
The tape will be placed along the gastrocnemius muscle, over the calcaneal fat pad, to the distal femur.
Tension in the KT group will be between 15-25%, with active stretching of the gastrocnemius muscle by the individual during taping.
|
KT will be applied by a certified physiotherapist following standardized procedures.
The skin of the lower leg will be cleaned with alcohol before application.
Participants will be positioned prone with their lower extremities fully extended, knees in full extension, and ankles in a neutral position.
The tape will be placed along the gastrocnemius muscle, over the calcaneal fat pad, to the distal femur.
Tension in the KT group will be between 15-25%, with active stretching of the gastrocnemius muscle by the individual during taping.
|
|
Placebo Comparator: Placebo group
The skin of the lower leg will be cleaned with alcohol before the procedure.
Participants will be positioned prone with their lower extremities fully extended, knees in full extension, and ankles in a neutral position.
The band will be placed along the gastrocnemius muscle, over the calcaneal fat pad, to the distal femur.
Tension will be achieved by leaving the band unstretched.
|
The skin of the lower leg will be cleaned with alcohol before the procedure.
Participants will be positioned prone with their lower extremities fully extended, knees in full extension, and ankles in a neutral position.
The band will be placed along the gastrocnemius muscle, over the calcaneal fat pad, to the distal femur.
Tension will be achieved by leaving the band unstretched.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Oxygenation Analysis of the Gastrocnemius Muscle
Time Frame: Before the application, at the 1st hour and at the 36th hour of the application
|
Before the application, at the 1st hour and at the 36th hour of the application
|
|
Pain Pressure Threshold
Time Frame: Before the application, at the 1st hour and at the 36th hour of the application
|
Before the application, at the 1st hour and at the 36th hour of the application
|
|
Analysis of the Mechanical Properties of the Gastrocnemius Muscle
Time Frame: Before the application, at the 1st hour and at the 36th hour of the application
|
Before the application, at the 1st hour and at the 36th hour of the application
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
May 15, 2026
Primary Completion (Estimated)
June 15, 2026
Study Completion (Estimated)
August 15, 2026
Study Registration Dates
First Submitted
April 29, 2026
First Submitted That Met QC Criteria
April 29, 2026
First Posted (Actual)
May 7, 2026
Study Record Updates
Last Update Posted (Actual)
May 7, 2026
Last Update Submitted That Met QC Criteria
April 29, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- IstanbulOkanUniv
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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