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临床试验/NCT02812459
NCT02812459已完成不适用

Short-term Effectiveness of Additional Electrical Stimulation to Exercise Versus Kinesio Taping in Patients With Chronic Low Back Pain: A Randomized Controlled Trial

Universidad de Granada2 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2016年6月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
62
试验地点
2
主要终点
Change from baseline in Roland Morris Disability Questionnaire (RMDQ) at one month.

研究概览

简要总结

The purpose of this study is to analyze the effectiveness of electrical stimulation and kinesio taping in combination with exercise in People with Chronic Low Back Pain

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 (Outcomes Assessor)

入排标准

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

入选标准

  • LBP for three months or more;
  • age between 25 and 65 years;
  • a score of four points or more on the Roland Morris Disability Questionnaire;
  • not currently receiving physical therapy.

排除标准

  • the presence of lumbar stenosis;
  • any clinical signs of radiculopathy;
  • a diagnosis of spondylolisthesis;
  • a diagnosis of fibromyalgia;
  • treatment with corticosteroid or oral medication within the past two weeks;
  • a history of spinal surgery;
  • disease of the central or peripheral nervous system.

研究组 & 干预措施

Kinesio taping plus exercise

Experimental

Kinesio taping application for low back plus back exercises.This protocol will be administered three a week for 4 weeks.

干预措施: Kinesio taping (Other)

Electrical stimulation plus exercise

Active Comparator

Electrical stimulation for control pain applied in low back plus exercises.This protocol will be administered three a week for 4 weeks.

干预措施: Electrical Stimulation (Other)

结局指标

主要结局

Change from baseline in Roland Morris Disability Questionnaire (RMDQ) at one month.

时间窗: 4 weeks

The Roland Morris disability questionnaire is a self-administered disability measurement scored on a 24-point scale from 0 = no disability to 24 = severe disability

次要结局

  • Change from baseline Visual Analogue Scale (VAS) at one month(4 weeks)
  • Change from baseline Pressure pain thresholds (PPT) at one month(4 weeks)
  • Change from baseline Tampa Scale for Kinesiophobia (TSK) at one month(4 weeks)
  • Change from baseline Oswestry Disability Index (ODI) at one month.(4 weeks)
  • Change from baseline Mechanosensitive/the Seated Slump Test neurodynamic testing at one month(4 weeks)
  • Change from baseline Mechanosensitive/straight-leg raise neurodynamic testing at one month(4 weeks)
  • Change from baseline Anxiety and depression measures at one month(4 weeks)
  • Change from baseline Quality of Sleep at one month(4 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Encarnación Aguilar Ferrandiz

Lecturer

Universidad de Granada

研究点 (2)

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