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临床试验/NCT05840666
NCT05840666已完成不适用

Effects of Mulligan Sustained Natural Apophyseal Glides Versus McKenzie Method of Mechanical Diagnosis & Therapy in Patients With Non-Specific Chronic Low Back Pain

Ayesha Jamil2 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2021年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
170
试验地点
2
主要终点
Pain Intensity

研究概览

简要总结

Low back pain (LBP) is the most frequent complaint encountered in clinical practice. Exercises and manual therapy prescription are common physical therapy treatments prescribed for the patients presenting with chronic low back pain. The interventions will establish the future direction for practitioners in choosing the manual therapy or repeated exercises as effective prescription and provide a basis for future research

详细描述

A variety of treatment interventions, modalities and techniques are used in physical therapy management of non-specific low back pain including manual therapy, exercises, neural mobilizations, stretching soft tissue techniques and dry needling etc. Out of these more recent literature supports manual therapy, self exercises, patient counseling and awareness have been recommended in back pain management guidelines, in the United States and is also frequently used in clinical practice in various countries.

Despite multiple theoretical frame works proposing the role of SNAGs and MDT mobilizations and exercises respectively, the literature on the true mechanism of direct or indirect physiological effects of these on performance or performance-related outcomes is vague and lacks justifiable procedural rigor.

The results of this study will provide information regarding the direction for practitioners in choosing the manual therapy or repeated exercises as effective prescription and provide a basis for future research.

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)

盲法说明

The outcome assessor will be unaware of the treatment group of study.

入排标准

年龄范围
20 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients of Both genders
  • Adult patents between the 20 to 45 years of age with chronic non-specific low back pain.
  • Pain intensity of at least 3 or greater on 0-10 Numeric Rating Scale.
  • Modified Low Back Pain Disability Questionnaire score equal to or greater than 20%.

排除标准

  • Serious underlying pathology with red flags.
  • Patients having contraindication to physical exercises.
  • Females with high parity.
  • Pregnant or lactating females.
  • Patients who participated in any type of rehabilitative training or exercise program for back pain in last 1 month.
  • Spinal deformity or Spinal stenosis.
  • History of fall or trauma to spine in last one year.
  • History of spinal, abdominal or hip surgery.
  • Signs of nerve root compression with sensory, motor or deep tendon reflexes deficit.
  • Serious underlying pathology with red flags.
  • Systemic disease e.g., cardiovascular, metabolic or central nervous system.
  • Osteopenia, osteoporosis.
  • Medication's history (steroids, immunosuppressants, chemotherapy)
  • Limb length discrepancy.

结局指标

主要结局

Pain Intensity

时间窗: Pain intensity will be recorded as baseline at the time of recruitment and change in pain intensity will be observed at follow up at the end of 3rd week of treatment.

Level of pain intensity will be measured using Numeric Rating Scale. The 11-point numeric scale ranges from '0' representing no pain to '10' representing the extreme pain

Lumbar Range of Motion

时间窗: Lumbar Range of Motion will be observed as baseline at the time of recruitment and change in ROM will be observed at follow up at end of 3rd week of treatment.

Lumbar Range of motion will be measured using inclinometers. Normal lumbar range of motion include 60 degrees of flexion, 25 degrees of extension, and 25 degrees of lateral bending

Level of Functional Disability

时间窗: Functional Disability will be recorded as baseline at the time of recruitment and change in score of functional disability will be recorded at the end of 3rd week of treatment.

Functional Disability will be measured with the Modified Low Back Pain Disability Questionnaire. The scores range from 0-100% with lower scores meaning less disability.

Change in Fear Avoidance Beliefs

时间窗: Fear Avoidance Beliefs will be observed as baseline at the time of recruitment and any change in Fear Avoidance Beliefs will be observed at the end of 3rd week of treatment.

Fear Avoidance Beliefs will be observed using Fear Avoidance Beliefs Questionnaire. There is a maximum score of 96. A higher score indicates more strongly held fear avoidance beliefs.

Change in Muscle Activation of Lumbar Multifidus (LM) and Transversus Abdominis (TrA)

时间窗: The Thickness of muscles will be recorded as baseline at the time of recruitment and change in thickness representing activation will be measured at follow up at the end of 3rd week of treatment.

Muscle Activation of Lumbar Multifidus (LM) and Transversus Abdominis (TrA) will be measured with Rehabilitative Ultrasound Imaging (RUSI).The activation of muscle is represented through change in thickness level of muscle observed through RUSI. The normal thickness of TrA is 3.93mm and LM is 28.99mm.

次要结局

未报告次要终点

研究者

发起方
Ayesha Jamil
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ayesha Jamil

Assistant Professor

University of Lahore

研究点 (2)

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