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临床试验/NCT07165249
NCT07165249已完成不适用

Positional Release Technique Versus Muscle Energy Technique For Patients With Non-Specific Low Back Pain With Facet Joint Restriction

Palestine Ahliya University2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2023年9月2日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
36
试验地点
2
主要终点
VAS - Baseline and after 4 weeks. Functional disability (Roland-Morris Questionnaire, RMQ) - Baseline and after 4 weeks.

研究概览

简要总结

Objective:The study aimed to compare the effectiveness of Positional Release Technique (PRT) and Muscle Energy Technique (MET) in reducing pain and improving outcomes for patients suffering from non-specific low back pain (NSLBP).

Materials and Methods: Thirty-six patients between the ages of 25 and 50, all referred by an orthopedic surgeon for treatment of non-specific low back pain (NSLBP), were enrolled in the study. Participants were randomly allocated into two groups (n=18 per group) using a computer-generated randomization sequence. However, details regarding allocation concealment and blinding of participants or assessors were not specified, which may influence the risk of bias. Group A received Positional Release Technique (PRT), while Group B received Muscle Energy Technique (MET). Prior to each treatment session, both groups received a standardized 15-minute hot pack application as a co-intervention to promote muscle relaxation and ensure consistency across interventions. Pain intensity was assessed using the Visual Analogue Scale (VAS), and functional outcomes were measured with the Roland-Morris Disability Questionnaire (RMQ). Participants in both groups attended three physiotherapy sessions per week over a four-week treatment period.

详细描述

  1. Study Identification

Official Title:

Positional Release Technique Versus Muscle Energy Technique for Patients with Non-Specific Low Back Pain With Facet Joint Restriction

Brief Title:

PRT vs MET in Non-Specific 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
None

入排标准

年龄范围
25 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Participants in the age category of 25 to 50 years old.
  • both male and female, with a diagnosis of low back pain (LBP), with or without referred leg pain.
  • chronic LBP lasting more than three months.

排除标准

  • Osteoporosis.
  • bone disease.
  • Spondylolisthesis.
  • History of vertebral fracture.
  • History of spinal surgery.

结局指标

主要结局

VAS - Baseline and after 4 weeks. Functional disability (Roland-Morris Questionnaire, RMQ) - Baseline and after 4 weeks.

时间窗: 4 weeks

A popular instrument for measuring pain is the visual analogue scale (VAS). Typically, it's a 10-cm line with the words "worst pain imaginable" at one end and "no pain" at the other. In order to quantify their level of pain, patients mark the line, and the distance from "no pain" serves as a proxy for pain

RMQ

时间窗: 4 weeks

It asks about 24 different activities and functions that could be impacted by back pain. Patients indicate if they now find it difficult to be active owing to back discomfort by answering "yes" or "no" to each topic. The total number of "yes" responses is added up to determine the score; a higher score denotes a larger disability

次要结局

未报告次要终点

研究者

发起方
Palestine Ahliya University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Azzam Alarab

Assistant Professor Chairperson, Department of Medical Sciences - Master's

Palestine Ahliya University

研究点 (2)

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