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NCT Number: NCT07606157

Effects of Kinesiotaping in Osteoarthritis

Knee osteoarthritis will be recognized as a leading cause of pain and functional disability, and conventional physiotherapy will remain a cornerstone of its management. Kinesiotaping will be widely used as an adjunct intervention; however, its additional benefit beyond standard rehabilitation programs will remain unclear.

This study will aim to investigate the additional effects of kinesiotaping combined with a conventional physiotherapy and rehabilitation program on pain, functional status, and kinesiophobia in individuals with unilateral knee osteoarthritis.

A total of 60 participants with unilateral knee osteoarthritis will be included in this randomized controlled trial and will be assigned to either a conventional physiotherapy (CP) group or a kinesiotaping (KT) group. Both groups will receive a 4-week (12 sessions) physiotherapy program including ultrasound, transcutaneous electrical nerve stimulation, patellofemoral mobilization, and exercise. Kinesiotaping will be applied every 3 days in the KT group. Outcome measures will include pain (VAS), kinesiophobia (TSK, FABQ), functional performance (30-s sit-to-stand, stair climb test), dynamic balance (functional reach), and WOMAC.

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Key information

Age range

40 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Knee osteoarthritis will be recognized as a leading cause of pain and functional disability, and conventional physiotherapy will remain a cornerstone of its management. Kinesiotaping will be widely used as an adjunct intervention; however, its additional benefit beyond standard rehabilitation programs will remain unclear.

This study will aim to investigate the additional effects of kinesiotaping combined with a conventional physiotherapy and rehabilitation program on pain, functional status, and kinesiophobia in individuals with unilateral knee osteoarthritis.

A total of 60 participants with unilateral knee osteoarthritis will be included in this randomized controlled trial and will be assigned to either a conventional physiotherapy (CP) group or a kinesiotaping (KT) group. Both groups will receive a 4-week (12 sessions) physiotherapy program including ultrasound, transcutaneous electrical nerve stimulation, patellofemoral mobilization, and exercise. Kinesiotaping will be applied every 3 days in the KT group. Outcome measures will include pain (VAS), kinesiophobia (TSK, FABQ), functional performance (30-s sit-to-stand, stair climb test), dynamic balance (functional reach), and WOMAC.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of unilateral grade 2 knee osteoarthritis,
  • Age between 40 and 65 years,
  • Ability to understand and comply with assessments and interventions,
  • Independent ambulation without assistive devices,
  • No participation in a physiotherapy program for knee-related complaints within the previous year

Exclusion criteria

  • History of lower extremity surgery or trauma,
  • Presence of neurological or orthopedic conditions affecting gait or physical function,
  • Allergic reaction to kinesiotape,
  • Inability to walk independently.

Treatment and study plan

Kinesiotaping

Other

Kinesiotaping

Primary outcomes

  1. Kinesiophobia

    Time frame: 4 weeks

    Kinesiophobia will evaluated using the Tampa Scale of Kinesiophobia (TSK) and the Fear-Avoidance Beliefs Questionnaire (FABQ). The TSK is a 17-item questionnaire scored on a 4-point Likert scale (1 = strongly disagree to 4 = strongly agree), with total scores ranging from 17 to 68, where higher scores indicate greater fear of movement. The FABQ assesses fear-avoidance beliefs related to physical activity and has been widely used in musculoskeletal disorders.

Secondary outcomes

  1. Pain intensity

    Time frame: 4 weeks

    Pain intensity will be assessed using the Visual Analog Scale (VAS), a 10-cm horizontal line ranging from "no pain" (0) to "worst imaginable pain" . Participants will be asked to indicate the intensity of their knee pain during activity, and the marked distance will be measured in centimeters

  2. Functional status

    Time frame: 4 weeks

    Functional status will be assessed using performance-based tests. The 30-Second Sit-to-Stand Test will be used to evaluate lower extremity muscle strength and endurance. Participants will be instructed to stand up and sit down as many times as possible within 30 seconds, and the total number of repetitions will be recorded .

  3. Functional mobility

    Time frame: 4 weeks

    The 12-Step Stair Climb Test will be used to assess functional mobility and lower limb performance. Participants will be asked to ascend and descend a 12-step staircase as quickly and safely as possible, and the total time taken to complete the task will be recorded in seconds .

  4. Dynamic balance

    Time frame: 4 weeks

    Dynamic balance will be evaluated using the Functional Reach Test. Participants will be instructed to stand upright and reach forward as far as possible without losing balance or taking a step. The maximum distance reached will be measured in centimeters .

Study contacts

Contact information is provided by the study sponsor or research team.

Nazli Assoc. Prof. Nazli Cigercioglu, Assoc. Prof.

CONTACT

[email protected]

+90 541 290 32 93

Sponsors and collaborators

Lead sponsor

Nazli Cigercioglu

Other

Registry information

Official study title

Effects of Adding Kinesiotaping to Conventional Physiotherapy on Pain, Function, and Kinesiophobia in Knee Osteoarthritis: A Randomized Controlled Trial

Acronym: Taping

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
May 26, 2026
Registry last updated
May 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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