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临床试验/NCT06267404
NCT06267404已完成不适用

Effectiveness of Iliopsoas Positional Release Versus Conventional Exercises in the Management of Sub-acute Back Pain in Pakistani Population

University of Karachi1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年2月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1
主要终点
VAS Visual Analogue Scale VAS Visual Analogue Scale

研究概览

简要总结

Recommended treatment for chronic non-specific LBP is exercise therapy, behavioral therapy including pain management, or a combination of these; There is not enough evidence to establish recommendations for which one is the most appropriate.

The primary objective of this study is to explore the effects of Ilio-psoas Release on Sub-acute back pain, ROM & functional disability

详细描述

Following the screening, participants will be randomized to receive the experimental or the controlled treatment in a1:1 ratio. Computer-generated random numbers will be used for Randomization. After obtaining the basic information, a unique code will be provided to each included patient. The outcome assessor will be blinded to the type of treatment. Patients and investigator could not be blinded due to the nature of treatment.

Group "A "(experimental group) will receive Positional Release Technique on Painful Iliopsoas(Both if Necessary) Group "B" (control group) will receive conventional physical therapy treatment consisting of hot pack, TENS, Ultra Sound along with back strengthening exercises.

All patients will be Assessed for Pain , ROM and Functional Activities before and after treatment sessions.

Visual Analogue Scale(VAS) and Modified Schober Test will be used for pain and ROM respectively. Roland-Morris Questionnaire (RMQ) will be used for functional activities.

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
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Sub-acute (pain for > 1.5 month)
  • Age 18-40 years
  • Willing to participate
  • Both gender will be recruited.

排除标准

  • Any history related to spinal surgery
  • Previous administration of epidural injections
  • LBP due to specific pathology
  • Neurological deficits (like stroke)
  • Clinical disorder contraindicated to exercise

结局指标

主要结局

VAS Visual Analogue Scale VAS Visual Analogue Scale

时间窗: Baseline and After Four weeks of Treatment

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 higher scores shows higher pain intensity and lower scores shows lower pain intensity.

Modified Schober's test

时间窗: Baseline and After Four weeks of Treatment

It is used during physical examination to assess the lumbar range of movement. It is highly co-related with lumbar range of movement measured through radiograph. Higher score reflect better range of motion of Spine.

次要结局

  • Roland-Morris Disability Questionnaire(Baseline and After Four weeks of Treatment)

研究者

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

Iram Iqbal Shamsi

Principle investigator

University of Karachi

研究点 (1)

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