跳至主要内容
临床试验/NCT06796881
NCT06796881招募中不适用

Instrument Assisted Soft Tissue Mobilization Versus Myofascial Release in Patients With Chronic Non¬Specific Low Back Pain

Cairo University1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2025年1月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
66
试验地点
1
主要终点
Assessing the change of pain intensity using visual analogue scale

研究概览

简要总结

This study was done to compare the effect of instrumental-assisted soft tissue mobilization versus the effect of myofascial release on pain intensity, pressure pain threshold, back function, and back range of motion in patients with chronic nonspecific low back pain.

详细描述

Low back pain affects 20% of the workforce annually, leading to increased work absenteeism. Chronic non specific low back pain restricts functional and occupational activities, impacting society and the economy. Treatment is often unsatisfactory, and there is no consensus on the optimal approach. Further scientific research is needed to understand the effects of facial tissue manipulation on Chronic non specific low back pain patients. The literature has not addressed the distinctions between myofascial force transmission instrumental assisted soft tissue mobilization and myofascial release on Chronic non specific low back pain patients, which could help physical therapists find effective treatments. This study is the first to include pain, Pressure pain threshold, back function, and range of motion as outcome measures and compare instrumental assisted soft tissue mobilization and myofascial release in Chronic non specific low back pain patients.

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
25 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with chronic non-specific low back pain for more than 3 months.
  • •Age between 25-45 years.

排除标准

  • •Patients who have serious spinal pathologies, such as fractures, tumors or inflammatory diseases (such as ankylosing spondylitis)
  • •Patients who have nerve root compromise, disk herniation, spondylolisthesis with neurological involvement, or narrowing of spinal canal
  • •Pregnant women
  • •Cancer patients .
  • •Lower limb injuries.
  • •Body mass index (BMI) greater than 25.

研究组 & 干预措施

Instrument assisted soft tissue mobilization group

Experimental

treatment group A involved 22 patients who will receive instrumental-assisted soft tissue mobilization and exercises

干预措施: Instrument assisted soft tissue mobilization (Other)

Instrument assisted soft tissue mobilization group

Experimental

treatment group A involved 22 patients who will receive instrumental-assisted soft tissue mobilization and exercises

干预措施: The conventional exercise program (Other)

Myofascial Release group

Active Comparator

treatment group B involved 22 patients who will receive myofascial release and exercises

干预措施: Myofascial release (Other)

Myofascial Release group

Active Comparator

treatment group B involved 22 patients who will receive myofascial release and exercises

干预措施: The conventional exercise program (Other)

Exercise only group

Active Comparator

control group (C) involved 22 patients who will receive exercises only.

干预措施: The conventional exercise program (Other)

结局指标

主要结局

Assessing the change of pain intensity using visual analogue scale

时间窗: at baseline and after 6 weeks

The visual analogue scale is a reliable tool for assessing chronic musculoskeletal pain, including chronic low back pain, with high correlations with verbal descriptive and numeric rating scales. It is a 10-cm line marked with no pain and severe pain, with higher scores indicating greater pain intensity.

次要结局

  • Assessing the change of pressure pain threshold using the pressure algometer(at baseline and after 6 weeks)
  • Assessing the change of flexion range of motion of the lumbar spine using the back range of motion device(at baseline and after 6 weeks)
  • Assessing the change of extension range of motion of the lumbar spine using the back range of motion device(at baseline and after 6 weeks)
  • Assessing the change of lateral flexion range of motion of the lumbar spine using the back range of motion device(at baseline and after 6 weeks)
  • Assessing the change of rotation range of motion of the lumbar spine using the back range of motion device(at baseline and after 6 weeks)
  • Assessing the change of back function using the 5) The Arabic version of Oswestry Disability Index(at baseline and after 6 weeks)

研究者

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

Dalia Salah Ahmed elshatoury

principal investigator

Cairo University

研究点 (1)

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