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GonarthrosisNCT07124169

Therapeutic Effects of Kinesiotape in the Management of Gonarthrosis

A study testing Kinesiotape + home exercise and Home exercise in people with Gonarthrosis, run by Fenerbahce University.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This randomized controlled trial evaluated the effectiveness of kinesiotaping in addition to exercise for patients with knee osteoarthritis (gonarthrosis). Thirty-eight participants aged 45 to 65 were randomly assigned to two groups: one group performed a structured home exercise program three times weekly for 6… Read more about this study

Who is it for?
Ages 45 to 65 years
Conditions the study is for
Gonarthrosis
What is being tested?
Kinesiotape + home exercise and Home exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
38 participants
Where
No sites listed yet
Study dates
Nov 2015to Jun 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 45 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • having a diagnosis of primary gonarthrosis according to ACR classification criteria,
  • being between 45 and 65 years of age,
  • having a radiological diagnosis of gonarthrosis between Kellgren-Lawrence stage 1-3 ,
  • signing the informed consent

Who cannot join

  • presence of a neurological disorder affecting muscle strength or balance,
  • history of any surgical operation on the knee, hip or spine,
  • physiotherapy or injections for the knee within the previous year,
  • presence of systemic conditions such as diabetes mellitus, vertigo, visual problems,
  • history of severe trauma within the previous year

About this study

Official title: Therapeutic Effects of Kinesiotape in the Management of Gonarthrosis: A Randomized Controlled Approach

This randomized controlled trial evaluated the effectiveness of kinesiotaping in addition to exercise for patients with knee osteoarthritis (gonarthrosis). Thirty-eight participants aged 45 to 65 were randomly assigned to two groups: one group performed a structured home exercise program three times weekly for 6 weeks, while the other group performed the same program and also received kinesiotaping once weekly. Outcomes included pain, stiffness, balance, and quality of life. Both groups demonstrated significant improvement; however, the kinesiotaping plus exercise group showed greater gains in pain reduction, mobility, and daily activities. These findings suggest that kinesiotaping combined with exercise may provide superior benefits compared with exercise alone in individuals with knee osteoarthritis.

Conditions
Gonarthrosis
Being tested
Kinesiotape + home exercise, Home exercise
Keywords
gonarthrosis, kinesiotape, home exercises
Medical subject headings
Osteoarthritis, Knee

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Kinesiotape + home exerciseOther

    Kinesiotaping will be applied to the knee once weekly for 6 weeks. In addition, participants will perform a structured home exercise program three times per week, including strengthening, stretching, and balance exercises.

  • Home exerciseOther

    In addition, participants will perform a structured home exercise program three times per week, including strengthening, stretching, and balance exercises.

Study groups in NCT07124169
Study groupRoleWhat they receive
Experimental (Kinesiotape+home exercise)ExperimentalThe taping procedure was repeated once a week, starting from the first week, for a total of 6 sessions. Mechanical correction technique and Ligament/Tendon correction technique, as kinesiotape application, were performed. ). A 6-week home exercise program was given to both the taping and control groups, three sessions per week. An individualized home exercise program was planned, considering EULAR and ACR recommendations. Each participant was given a structured home exercise program for approximately 30 minutes per day, at least 3 days a week. The program included moderate-intensity aerobic exercises (e.g., walking) and muscle-strengthening exercises targeting the quadriceps and hamstring muscles, along with flexibility and balance exercises. ).
Receives: Other: Kinesiotape + home exercise
control (home exercise )Active comparatorA 6-week home exercise program was given to both the taping and control groups, three sessions per week. An individualized home exercise program was planned, considering EULAR and ACR recommendations. Each participant was given a structured home exercise program for approximately 30 minutes per day, at least 3 days a week. The program included moderate-intensity aerobic exercises (e.g., walking) and muscle-strengthening exercises targeting the quadriceps and hamstring muscles, along with flexibility and balance exercises.
Receives: Other: Home exercise

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

    WOMAC consists of 24 questions in total (pain 5, joint stiffness 2, functional status 17). Each question was scored on a scale of 1-5. A high score indicates poor health, while a low score indicates good health.

    Measured: From enrollment to the end of treatment at 6 weeks

Secondary outcomes (3)
  1. Visual Analogue Scale (VAS)

    VAS, which ranges from 0 to 10, is used to assess pain levels. A score of 0 represents no pain, while 10 indicates the most severe, unbearable pain. Participants were instructed to indicate their perceived pain level by marking a 10 cm straight line, and the corresponding value was recorded in centimeters.

    Measured: From enrollment to the end of treatment at 6 weeks

  2. Berg Balance Scale (BBS)

    BBS is a test consisting of 14 items used to evaluate the functional balance of individuals. The application time is approximately 15-20 minutes, and the following materials are needed: a ruler, a stopwatch, a chair, a step, and an area suitable for 360-degree rotation. Each item is evaluated on a scale of 0-4 points based on the individual's ability to perform the given task independently and correctly. The total score is 56. A score between 0-20 indicates severe balance impairment, between 21-40 indicates acceptable balance, and between 41-56 indicates good balance.

    Measured: From enrollment to he end of treatment at 6 weeks.

  3. Short Form (SF-36)

    The SF-36 questionnaire was developed to assess quality of life. A total of 8 sub-parameters, including pain, social functioning, energy/vitality, emotional role difficulties, physical role difficulties, physical functioning, general health perception, and mental health, are examined

    Measured: From enrollment to the end of treatment at 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Aug 2025
  2. Study startNov 2015
  3. Primary completionJan 2016
  4. Study completionJun 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
38 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07124169
Sponsor's protocol ID
2015-17/04
Status last verified
Aug 2025
First submitted
5 Aug 2025
Last updated
15 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared due to concerns regarding patient confidentiality and data privacy

Questions about this trial

What is this clinical trial studying?

A study testing Kinesiotape + home exercise and Home exercise in people with Gonarthrosis, run by Fenerbahce University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) (time frame: From enrollment to the end of treatment at 6 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Aug 2025.

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