跳至主要内容
临床试验/NCT06611709
NCT06611709已完成不适用

Effectiveness of the Kinesiotaping in the Treatment of Chronic Lateral Epicondylitis: a Randomized, Sham-controlled, Single-blind Study

Konya Beyhekim Training and Research Hospital2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2024年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
42
试验地点
2
主要终点
Patient-Rated Tennis Elbow Evaluation Questionnaire (PRTEE)

研究概览

简要总结

Lateral epicondylitis significantly impacts daily activities and productivity at work, making it a condition of substantial clinical and socioeconomic importance.Despite its high prevalence, clinical significance, and impact on daily life, the optimal management of LE remains a topic of ongoing debate.

This study aims to investigate the efficacy of kinesiotaping (KT) on pain intensity, functional status, and quality of life in patients with chronic lateral epicondylitis (LE).

The study was conducted in the outpatient clinic for level 3 physical medicine and rehabilitation. Patients were randomized into two groups: the real kinesiotaping + home exercise group and the sham taping + home exercise group (randomized by a medical secretary outside the study). A set of widely accepted, literature-consistent primer and seconder outcomes were statistically compared to determine whether one treatment was superior to the other.

详细描述

Between February 1, 2024, and August 31, 2024, a total of 42 patients (17 females, 25 males) with chronic LE were included. Patients were randomized into either the KT or sham-controlled group. Patients were blinded to which group they were assigned to. The taping was performed by the same physician, who was trained and experienced in kinesiotaping.

Kinesiotaping and sham-taping were applied six times over three weeks. Both groups received recommendations for activity modification and a home-based stretching and strengthening exercise program. The exercise program was designed by an author who has a national book chapter on exercise for the treatment of lateral epicondylitis, taking into account patient specificity and adherence, and in accordance with the literaturExercise adherence was monitored through weekly outpatient controls (while taping) and by phone check-ins two weeks after the taping was completed.

Outcome measures were visual analog scale (VAS) pain score, Patient-Rated Forearm Evaluation Questionnaire (PRFEQ), grip strength, Disabilities of Arm, Shoulder, and Hand (DASH), quality of life in Short Form-36 (SF-36), and The Roles and Maudsley patient satisfaction score. The subjects were assessed before treatment, at the end of treatment (week three), and four weeks after the end of treatment (week seven).The assessment parameters were also conducted by the same researcher to ensure consistency.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults aged 18 to 65 years
  • A pain severity of 4 or higher on the visual analog scale (VAS) during daily activities
  • A history of lateral epicondylitis symptoms lasting at least three months

排除标准

  • Communication difficulties
  • Significant psychiatric disorders
  • A history of trauma within the past six months
  • Neuromuscular conditions
  • Abnormalities of the upper limb
  • Prior upper limb surgery
  • A history of rheumatic diseases
  • Cervical disc pathology, polyneuropathy, or hand disorders (such as carpal or cubital tunnel syndrome, de Quervain tenosynovitis, osteoarthritis)
  • Receipt of any treatment for lateral epicondylitis (e.g., local injections, physical therapy, splints) within the last six month

结局指标

主要结局

Patient-Rated Tennis Elbow Evaluation Questionnaire (PRTEE)

时间窗: baseline, week 3, and week 7

0 (best) to 100 (worst)

VAS pain (0-10)

时间窗: baseline, week 3, and week 7

0 no pain; 10 unbearable/max. pain.

次要结局

  • The Disabilities of the Arm, Shoulder, and Hand (DASH)(baseline, week 3, and week 7)
  • grip strength(baseline, week 3, and week 7)
  • The Short Form-36 (SF-36) quality of life index(baseline, week 3, and week 7)
  • Patient satisfaction/benefit scale (The Roles and Maudsley score)(baseline, week 3, and week 7)

研究者

发起方
Konya Beyhekim Training and Research Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Ramazan Yılmaz

Associate Prof

Konya Beyhekim Training and Research Hospital

研究点 (2)

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