跳至主要内容
临床试验/CTRI/2018/07/014800
CTRI/2018/07/014800尚未招募不适用

TO STUDY THE COMBINED EFFECT OF PAIN NEUROSCIENCE EDUCATION WITH EXERCISES IN COMPARISON WITH PAIN NEUROSCIENCE EDUCATION AND EXERCISES ALONE IN PATIENTS WITH CHRONIC LOW BACK PAIN- A RANDOMIZED CONTROLLED TRIAL.

Apurva Sanjay Kadam1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2018年7月16日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
90
试验地点
1
主要终点
1.visual analogue scale.

研究概览

简要总结

Numerous studies have been done tofind out the effectiveness of pain neuroscience education in patients withchronic low back pain combined with other treatment techniques. But there is lack of evidence showing use of pain neuroscience education withexercise protocol (stretching and strengthening) in patients with chronic lowback pain. Also the effectiveness of these protocols combined with painneuroscience education cannot be judged because of the absence of a controlgroup.  Most of the studies are done inthe western countries and other parts of the world, but studies are lacking inIndia. Thus, a very strong need arises to find out the combined effect of painneuroscience education with exercises in comparison to pain neuroscienceeducation and exercises alone on pain intensity, disability, quality of lifeand fear associated in patients with chronic low back pain.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • Patients having low back pain of more than 12 weeks.
  • Patients aged 18-80 years.

排除标准

  • 1.Low back pain less than 3 months (12 weeks).
  • 2.Suspected spinal pathology like -malignancies, Unhealed vertebral fractures, ankylosing spondylitis, Inflammatory arthritis, radicular syndrome Cauda equina syndrome.
  • 3.Pregnancy.
  • 4.Patients with vision, speech and auditory disorders.
  • 5.Uncontrolled mental health abnormalities like- Bipolar disorder, schizophrenia, major depressive disorder.
  • 6.Unwilling to participate voluntarily.
  • 7.Involvement of other systems/multiple systems issues.

结局指标

主要结局

1.visual analogue scale.

时间窗: 3 weeks, 2 sessions per week. | outcome measures will be assessed at baseline and after 3 weeks.

次要结局

  • 1.Oswestry disability index.(2. SF-36 Quality of life questionnaire.)

研究者

发起方
Apurva Sanjay Kadam
申办方类型
Other [self]

研究点 (1)

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