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临床试验/NCT05428280
NCT05428280已完成不适用

Effectiveness of Muscle Energy Technique Versus Myofascial Mobilization in Improving Functional Outcome in Sub-acute Non-specific Low Back Pain: A Randomized Controlled Trial

Dow University of Health Sciences1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年12月22日最近更新:
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
60
试验地点
1
主要终点
Visual Analogue Scale

研究概览

简要总结

Institute for Clinical Systems Improvement (ICSI) defines sub-acute low back pain as low back pain lasting between 4 and 12 weeks. There is insufficient evidence regarding the comparative effect of muscle energy technique and myofascial mobilization in the management of sub-acute non-specific low back pain with the tightness of quadratus lumborum and erector spinae muscles

详细描述

A randomized experimental controlled trial will be carried out to compare the effectiveness of muscle energy technique and myofascial mobilization in the management of sub-acute non-specific low back pain. A total of 60 male and female volunteers having subjects with sub-acute nonspecific low back pain will be recruited in this study. Subjects will be assessed at baseline for pain and disability using Visual Analogue Scale and Ronald Morris Disability Questionnaire (RMDQ 0-24) respectively. After baseline assessment, all subjects will be allocated to two groups through computer-generated random sampling. Group 1 will perform Muscle energy technique combined with conventional exercise; Group 2 will receive Myofascial Mobilization combined with conventional exercise. This study will be conducted at the Physiotherapy Department of Sindh Institute of Physical Medicine and Rehabilitation (SIPM&R). Data will be analyzed using SPSS 21 and ANCOVA technique will be used in this 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
Single (Outcomes Assessor)

入排标准

年龄范围
30 Years 至 55 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Sub-acute low back pain with the range of 7 to 12 weeks of unresolved symptoms.
  • •Positive test of tight Erector spinae muscle and Tight Quadratus Lumboram muscle

排除标准

  • •Spinal malignancy
  • •Spinal fracture
  • •Spine foraminal stenosis
  • •Nerve root compression
  • •Radicular symptoms
  • •Cord compression
  • •Paralysis
  • •Muscular dystrophy
  • •Myelopathy
  • •Seizure disorder
  • •Severe trauma
  • •Unexplained weight loss

研究组 & 干预措施

Muscle Energy Techniques

Experimental

Following physiotherapy will be given to the participants in this group for 4 weeks, 3 times a week:

1. Muscle Energy Technique

干预措施: Physiotherapy (Other)

Muscle Energy Techniques

Experimental

Following physiotherapy will be given to the participants in this group for 4 weeks, 3 times a week:

1. Muscle Energy Technique

干预措施: Muscle Energy technique (Other)

Myofascial Mobilization Techniques

Active Comparator

Following physiotherapy will be given to the participants in this group for 4 weeks, 3 times a week:

1. Myofascial Mobilization

干预措施: Physiotherapy (Other)

Myofascial Mobilization Techniques

Active Comparator

Following physiotherapy will be given to the participants in this group for 4 weeks, 3 times a week:

1. Myofascial Mobilization

干预措施: Myofacial mobilization (Other)

结局指标

主要结局

Visual Analogue Scale

时间窗: Change from baseline pain intensity at 4 weeks

The visual analogue scale is used for measurement of pain intensity. It is a continuous scale. It comprises a horizontal or vertical 10 centimeters or 100 millimeters line. The participant is asked to indicate a point of pain intensity by placing a line perpendicular to the Visual analogue scale line. The scale is most commonly referred by "no pain" with score of 0 and "worst imaginable pain" with score of 100 on the scale. The higher scores shows higher pain intensity and lower scores shows lower pain intensity.

Rolland Morris Disability Questionnaire

时间窗: Change from baseline functional disability at 4 weeks

It is a standard questionnaire with questions regarding pain and the disabling effect on daily activities. Its score ranges from 0 to 24 (no disability to maximum disability)

次要结局

未报告次要终点

研究者

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

Faizan Abdullah

Principal Investigator

Dow University of Health Sciences

研究点 (1)

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