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临床试验/NCT06568796
NCT06568796已完成不适用

Comparison of the Effects of Trigger Point Ischemic Compression Massage and Focused Extracarporeal Shock Wave Therapy on Pain Level, Muscle Strength, Joint Range of Motion, Functionality and Quality of Life in Patients With Lateral Epicondylitis: a Randomized Controlled Trial

Ankara Yildirim Beyazıt University2 个研究点 分布在 2 个国家目标入组 75 人开始时间: 2023年6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
75
试验地点
2
主要终点
range of motion asessment with universal goniometer

研究概览

简要总结

To compare the effects of Trigger Point Ischaemic Compression Massage (TPICM) and Focused Extracarporeal Shock Wave Therapy (focused ESWT) on pain level, muscle strength, Joint range of motion, functionality and quality of life in patients with lateral epicondylitis (LE) in a randomised controlled trial.

详细描述

The study was planned to include at least 66 patients who presented to the sports medicine clinic of Gülhane Training and Research Hospital with lateral epicondyle pain for at least 2 months, were diagnosed with lateral epicondylitis and verbally and in writing declared that they were willing to participate in the study.

Patients participating in the study;

  1. assessment of pain intensity with visual analog scale (VAS)
  2. Evaluation of hand grip strength with jamar hand dynamometer
  3. Isokinetic muscle strength assessment of wrist muscles with biodex isokinetic system 3
  4. assessment of wrist range of motion with a manual goniometer
  5. Function assessment with PRTEE-T
  6. DASH questionnaire
  7. SF-36 quality of life assessment will be performed before and after treatment.

inclusion criteria

  1. Male and female individuals aged 18-60 years
  2. being diagnosed with lateral epicondilitis
  3. volunteering to participate in the study

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 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Male and female individuals between the ages of 18-60
  • being diagnosed with lateral epicondylitis
  • volunteering to participate in the study

排除标准

  • non-cooperation
  • presence of systemic and metabolic diseases
  • malignancy, osteoporosis, fracture, blood clotting disorder, pacemaker, infection
  • utilization of another treatment for lateral epicondylitis during the study period
  • previous invasive treatment with steroids for lateral epicondylitis
  • any treatment for lateral epicondylitis in the last 6 months

结局指标

主要结局

range of motion asessment with universal goniometer

时间窗: baseline-up to 4 weeks

It will be elbow range of motion asessment with universal goniometer

pain level asessment with visual analog scale

时间窗: baseline-up to 4 weeks

It will be asessment of pain level with visual analog scale

grip strenght asessment with jamar hand dynamometer

时间窗: baseline-up to 4 weeks

It will be grip strength assessment with jamar hand dynamometer

muscle strenght asessment with isocinetic system

时间窗: baseline-up to 4 weeks

It will be elbow flexor and extansor muscle strength asessment with isocinetic system

assessment of quality of life with quality of life questionnaire

时间窗: baseline-up to 4 weeks

It will be asessment of quality of life with life questionnaire

assessment of functionality with functionality questionnaire

时间窗: baseline-up to 4 weeks

It will be asessment of functionality with functionality questionnaire

次要结局

未报告次要终点

研究者

发起方
Ankara Yildirim Beyazıt University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Bihter Aslanyurek

Associate Professor

Ankara Yildirim Beyazıt University

研究点 (2)

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