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CompletedNCT07840690Updated Sep 25, 2026

Effects of Kinesio Taping on Delayed-Onset Muscle Soreness and Functional Recovery

An interventional study of Kinesio Taping in Delayed-Onset Muscle Soreness, sponsored by Firat University. Completed at 1 site in Turkey (Türkiye). Open to male participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-25.

Sponsored by Firat University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 5 months after the study started (first participant enrolled Mar 2025, registered Sep 2026).
Updated Sep 25, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Randomized
Ages
18 Years to 25 Years
Sex
Male
01

Study summary

This study evaluates the effects of kinesio taping applied to the quadriceps femoris on delayed-onset muscle soreness, lower-extremity range of motion, and explosive jump performance following a fatiguing exercise protocol in healthy sedentary males.

Read the detailed description

Participants undergo a fatiguing sit-to-stand exercise protocol to induce exercise-induced muscle damage. Using a controlled crossover design with repeated measurements, participants complete both a kinesio taping (KT) condition and a non-taping (N-KT) control condition, separated by a 96-hour washout period. Measurements including subjective muscle soreness, active range of motion of the hip, knee, and ankle joints, thigh circumference, and squat jump performance are evaluated at baseline, 24, 48, and 72 hours post-exercise.

02

Conditions studied

  • Delayed-Onset Muscle Soreness

Browse trials for

Keywords

  • Kinesio Taping
  • DOMS
  • Recovery
  • Squat Jump
03

In context

Myalgia

256 studies on the registry are indexed under Myalgia; 46 are open to participants now.

This study's enrollment of 15 is below the median of 44 across 216 interventional studies indexed under Myalgia.

Browse Myalgia studies →

Lead sponsor

Firat University is the lead sponsor of 117 studies on the registry; 46 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 25 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

  • Healthy male participants aged between 18 and 25 years.
  • Individuals with a sedentary lifestyle, defined as no regular exercise participation during the past six months.

Exclusion criteria

Exclusion Criteria:

  • Individuals with a history of lower extremity musculoskeletal injury within the previous six months.
  • Known skin or allergic reactions to acrylic adhesives.
  • Current use of non-steroidal anti-inflammatory drugs (NSAIDs), analgesics, or antioxidant supplements.
  • Application of external recovery modalities, including massage or cryotherapy, during the study period.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
15 participants (actual)

Study arms

  • Experimental
    Kinesio Taping (KT)

    Application of Y-shaped kinesio tape to the quadriceps femoris muscle with 25%-50% tension immediately after the fatigue protocol.

    Device: Kinesio Taping

  • No intervention
    Non-Taping Control (N-KT)

    Participants complete the fatiguing protocol without any taping application during the recovery period.

Interventions

  • DeviceKinesio Taping

    Therapeutic taping applied to the anterior thigh to evaluate recovery kinetics.

06

What researchers measure

Primary outcomes

  1. Delayed-Onset Muscle Soreness (DOMS)

    Assessed using the Visual Analog Scale (VAS), where scores range from 0 (no pain) to 10 (very severe pain).

    Time frame: Baseline (0 hour), 24 hours, 48 hours, and 72 hours post-exercise

Secondary outcomes

  1. Squat Jump Performance

    Assessed using a digital contact mat system to measure explosive jump height in centimeters.

    Time frame: Baseline (0 hour), 24 hours, 48 hours, and 72 hours post-exercise

  2. Joint Range of Motion (ROM)

    Active range of motion of hip, knee, and ankle joints measured in degrees using a universal goniometer.

    Time frame: Baseline (0 hour), 24 hours, 48 hours, and 72 hours post-exercise

  3. Thigh Circumference

    Measured in centimeters at the marked anatomical landmark (15 cm proximal to the superior border of the patella) to track tissue edema.

    Time frame: Baseline (0 hour), 24 hours, 48 hours, and 72 hours post-exercise

07

Study locations

1 site
  • Firat University, Faculty of Sport Science
    Elâzığ, Elâzığ 23119, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Yes — The datasets generated and/or analysed during the current study are available from the corresponding author on reasonable request.

Supporting information: Study protocol

Time frame: Following publication of the study results.

Access criteria: Upon reasonable request directed to the corresponding author via email.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Mar 2025 to primary completion in May 2025, 1 month.

Of 101 non-industry interventional studies with no phase under Myalgia, half reached primary completion within 8 months of starting (the median), counting those still running; a quarter within 3 and three quarters within 16. This study's 1 month is below that.

Counting every sponsor, half of 111 studies reached it within 8 months; a quarter within 3 and three quarters within 16.

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

Registered
Sep 19, 2026
First posted
Sep 25, 2026
StartActual
Mar 20, 2025
Primary completionActual
May 10, 2025
CompletionActual
May 20, 2025
Last update
Sep 25, 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.
Registered
First appeared on the registry. No changes since
Sep 25, 2026
Show all 1 update
  1. Sep 25, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07840690
Lead sponsor
Firat University
Responsible party
Taner Akbulut (Prof., Firat University) — Principal investigator
First posted
Sep 25, 2026
Start date
Mar 20, 2025
Primary completion
May 10, 2025
Completion
May 20, 2025
Last update
Sep 25, 2026

Oversight

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

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This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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