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临床试验/NCT07574307
NCT07574307招募中不适用

The Effect of Kinesiotaping on Pain and Functionality in Isolated Meniscus Injuries: A Randomized Controlled Study

Bandırma Onyedi Eylül University1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2026年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
75
试验地点
1

研究概览

简要总结

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

详细描述

Our 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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究者

发起方
Bandırma Onyedi Eylül University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Nurten NAS KIRDAR

Assistant Professor

Bandırma Onyedi Eylül University

研究点 (1)

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