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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

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

Keywords

  • Kinesio Taping
  • DOMS
  • Recovery
  • Squat Jump
03

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

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 hypersensitivity 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.
04

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.

05

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

06

Study locations

1 site
  • Firat University, Faculty of Sport Science
    Elâzığ, Elâzığ 23119, Turkey (Türkiye)
07

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

No publications or documents are linked to this record.

08

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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