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Clinical Trials/NCT05840666
NCT05840666
Completed
Not Applicable

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

Ayesha Jamil1 site in 1 country170 target enrollmentJanuary 1, 2021
ConditionsLow Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Ayesha Jamil
Enrollment
170
Locations
1
Primary Endpoint
Pain Intensity
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

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

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
June 15, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Ayesha Jamil
Responsible Party
Sponsor Investigator
Principal Investigator

Ayesha Jamil

Assistant Professor

University of Lahore

Eligibility Criteria

Inclusion Criteria

  • 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%.

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

Pain Intensity

Time Frame: 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

Time Frame: 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

Time Frame: 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

Time Frame: 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)

Time Frame: 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.

Study Sites (1)

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