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Not yet recruitingNCT07572201Updated May 7, 2026

The Effect of Kinesio Taping Applied to the Gastrocnemius Muscle on Muscle Oxygenation, Pain Pressure Threshold, and Muscle Mechanical Properties

An interventional study of Kinesio® tape application and Placebo in Kinesio Taping and Muscle Oxygenation, sponsored by Okan University. Not yet recruiting. Open to male participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-07.

Sponsored by Okan University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Jun 2026, 4 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
Male
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Kinesio Taping
  • Muscle Oxygenation
03

In context

Lead sponsor

Okan University is the lead sponsor of 97 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Right lower extremity being dominant,
  • Not having suffered a musculoskeletal injury to the lower extremity in the last 3 months

Exclusion criteria

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.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
50 participants (estimated)

Study arms

  • 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.

    Other: Kinesio® tape application

  • 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.

    Other: Placebo

Interventions

  • OtherKinesio® tape application

    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.

  • OtherPlacebo

    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.

06

What researchers measure

Primary outcomes

  1. Oxygenation Analysis of the Gastrocnemius Muscle

    Time frame: Before the application, at the 1st hour and at the 36th hour of the application

  2. Pain Pressure Threshold

    Time frame: Before the application, at the 1st hour and at the 36th hour of the application

  3. 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

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for May 2026; primary completion for Jun 2026, 1 month later.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 29, 2026
First posted
May 7, 2026
StartEst.
May 15, 2026
Primary completionEst.
Jun 15, 2026
CompletionEst.
Aug 15, 2026
Last update
May 7, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07572201
Lead sponsor
Okan University
Responsible party
Kübra Kendal (PhD, Okan University) — Principal investigator
First posted
May 7, 2026
Start date
May 15, 2026 (estimated)
Primary completion
Jun 15, 2026 (estimated)
Completion
Aug 15, 2026 (estimated)
Last update
May 7, 2026

Study contacts

Kubra Kendal
Contact
kubra.kendal@okan.edu.tr
+90 530-233-8078

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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