ClinicalTrials.gg
RecruitingNCT07574307Updated Oct 2, 2026

Kinesiotaping in Isolated Meniscus Injuries

An interventional study of sham taping and Exercise in Meniscus Injury and Kinesio Taping, sponsored by Bandırma Onyedi Eylül University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-10-02.

Sponsored by Bandırma Onyedi Eylül University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Apr 2026; still recruiting 7 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

The effect of kinesiotaping on pain and functionality in isolated meniscus injuries.

Read the detailed description

This study was designed as a randomized controlled trial. All patients presenting to the Physical Medicine and Rehabilitation outpatient clinic with knee pain and meeting the inclusion criteria will be included in the study after being informed and giving their consent. Patients' age, gender, and body mass index will be recorded. Patients will be divided into three groups using stratified randomization. An attempt will be made to ensure a homogeneous distribution of patients in terms of gender, age, and body mass index. Group 1 will receive standard treatment, Group 2 will receive standard treatment + kinesiotaping, and Group 3 will receive standard treatment + sham taping. Standard treatment will consist of strengthening exercises for the quadriceps and hamstring muscles, stretching exercises around the knee, proprioceptive exercises, and activity modification. These exercises will be taught to the patient and they will be asked to perform them at home five days a week for three weeks. Kinesiotaping and sham taping will be applied three times, once every five days. Kinesiotaping will be applied to the group with a specific tension and technique (quadriceps facilitation technique, "Y" tape shape, applied with 25-50% tension), while the sham group will have the tape simply applied to the skin without any tension (perpendicular to the quadriceps muscle, tension-free). Kinesiotapes do not contain any medication; their effect depends on the technique (facilitation, inhibition, etc.) and tension level (10%, 25%, 50%, 75%). All patients will have VAS and WOMAC parameters evaluated before treatment, on day 20, and at month 3 after treatment.

02

Conditions studied

  • Meniscus Injury
  • Kinesio Taping

Keywords

  • meniscus
  • knee injuries
  • pain
  • functional status
  • kinesio taping
03

In context

Knee Injuries

267 studies on the registry are indexed under Knee Injuries; 59 are open to participants now.

This study's planned enrollment of 75 is above the median of 49 across 178 interventional studies indexed under Knee Injuries.

Browse Knee Injuries studies →

Lead sponsor

Bandırma Onyedi Eylül University is the lead sponsor of 70 studies on the registry; 19 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Ages 18-50
  • Knee pain lasting longer than 2 weeks
  • Having a diagnosis of isolated meniscus injury (grade 1, 2 or 3 meniscus degeneration) confirmed by magnetic resonance imaging (MRI)
  • Not having undergone knee surgery in the last 6 months
  • Not having received intraarticular injections in the knee area
  • Being willing to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Trauma history
  • Anterior or posterior cruciate ligament injury
  • Collateral ligament injuries
  • Advanced knee osteoarthritis
  • Rheumatic or neurological disease
  • Allergy or skin condition to kinesiotape
  • History of intraarticular injection
  • Neuromuscular dysfunction
  • Rheumatological disease
  • Cognitive dysfunction
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
75 participants (estimated)

Study arms

  • Experimental
    Exercises

    Standard treatment will consist of strengthening exercises for the quadriceps and hamstring muscles, stretching exercises around the knee, proprioceptive exercises, and activity modification. These exercises will be taught to the patient and they will be asked to perform them at home five days a week for three weeks.

    Behavioral: Exercise

  • Experimental
    kinesiotaping

    Kinesiotaping will be applied three times, once every five days. Kinesiotaping will be applied to the group with a specific tension and technique (quadriceps facilitation technique, "Y" tape shape, applied with 25-50% tension). Kinesiotapes do not contain any medication; their effect depends on the technique (facilitation, inhibition, etc.) and tension level (10%, 25%, 50%, 75%).

    Procedure: kinesiotaping

  • Experimental
    sham taping

    Sham taping will be applied three times, once every five days. The sham group will have the tape simply applied to the skin without any tension (perpendicular to the quadriceps muscle, tension-free). Kinesiotapes do not contain any medication; their effect depends on the technique (facilitation, inhibition, etc.) and tension level (10%, 25%, 50%, 75%).

    Procedure: sham taping

Interventions

  • Proceduresham taping

    sham taping will be applied three times, once every five days. the sham group will have the tape simply applied to the skin without any tension (perpendicular to the quadriceps muscle, tension-free). Kinesiotapes do not contain any medication; their effect depends on the technique (facilitation, inhibition, etc.) and tension level (10%, 25%, 50%, 75%).

  • BehavioralExercise

    rengthening exercises for the quadriceps and hamstring muscles, stretching exercises around the knee, proprioceptive exercises, and activity modification.

  • Procedurekinesiotaping

    Kinesiotaping will be applied three times, once every five days. Kinesiotaping will be applied to the group with a specific tension and technique (quadriceps facilitation technique, "Y" tape shape, applied with 25-50% tension). Kinesiotapes do not contain any medication; their effect depends on the technique (facilitation, inhibition, etc.) and tension level (10%, 25%, 50%, 75%).

06

What researchers measure

Primary outcomes

  1. VAS

    The VAS (Visual Analog Scale) will be used to determine the severity of knee pain. The VAS is a reliable and easily applicable scale accepted worldwide in the literature for measuring the severity of pain in patients. The Visual Analog Scale is used to convert values that cannot be measured numerically into numerical values. It is a scale where the starting point is -0- "no pain" and the other end is -10- "very severe pain," with numerical values assigned to each centimeter (cm) in one-centimeter increments.

    Time frame: 3 months

  2. WOMAC

    The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) is a widely used, valid, and reliable index for evaluating patients with osteoarthritis. It is also very commonly used in knee problems other than osteoarthritis to assess knee pain and knee function. It is a recommended metric for osteoarthritis studies by the Outcome Measures in Rheumatology Clinical Trials (OMERACT). The WOMAC OA index, validated and proven reliable in Turkish by Tüzün et al., consists of three sections and 24 questions assessing pain, stiffness, and physical function. The maximum possible scores are 20 for the pain subgroup, 8 for stiffness, and 68 for physical function. Higher scores indicate increased pain and stiffness, and impaired physical function.

    Time frame: 3 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Publications

  • Randazzo E, Duerr R, Baria MR. Meniscus Root Tears: A Clinical Review. Curr Sports Med Rep. 2022 May 1;21(5):155-158. doi: 10.1249/JSR.0000000000000959. PubMed 35522439 ↗
  • Ahmed MM, Zaino M, Moustafa M, Alajam RA, Alameer AH, Morsy WE, Fayed EM, Malik S, Amin WM. Kinesio Taping Increases Peak Torque of Quadriceps Muscle After Arthroscopic Meniscectomy, Double-Blinded RCT. Int J Gen Med. 2024 May 6;17:1897-1908. doi: 10.2147/IJGM.S463753. eCollection 2024. PubMed 38736667 ↗

Individual participant data

Plan to share: No — Once our study is completed, if it is deemed suitable for evaluation and publication in a peer-reviewed journal on the subject, all researchers will be able to access our results.

09

Updates

1 registry update since Sep 25, 2026
Minor edits
Nothing that changes what the study is or who can join. Edited: description
1 update, last Oct 2, 2026
Show all 1 update
  1. Oct 2, 2026
    Minor edits only
    + 1 other change: description

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
NCT07574307
Lead sponsor
Bandırma Onyedi Eylül University
Responsible party
Nurten NAS KIRDAR (Assistant Professor, Bandırma Onyedi Eylül University) — Principal investigator
First posted
May 7, 2026
Start date
Apr 1, 2026
Primary completion
Oct 30, 2026 (estimated)
Completion
Oct 30, 2026 (estimated)
Last update
Oct 2, 2026

Study contacts

Nurten NAS KIRDAR, Assistant Professor
Contact
nkirdar@bandirma.edu.tr
+905415511691
Nurten NAS KIRDAR, Assistant Professor
principal investigator · Bandırma Onyedi Eylül University

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion