Objectives: To investigate the effectiveness of instrument-based mobilization compared with manual mobilization in patients with non-specific low back pain (NLBP), in terms of spinal muscle activation, decrease in pain, and improvement in range of motion (ROM). Design: Randomized clinical trial, double blind. Participants and interventions: A total of 66 participants with localized NLBP will be divided into 2 groups matched for sex, age, and body mass index. The intervention group will receive central postero-anterior mobilization with a force of 150 N through physiotherapy instrument mobilization at the level of pain in the lumbar spine. The control group will receive central postero-anterior grade III mobilization through the pisiform grip method at the level of pain in the lumbar spine. Main outcome measures: Measurements will be taken before the intervention, after the 1st session, after the 6th session, and at 4 weeks follow-up. Rehabilitative ultrasound imaging will be done to identify lumbar multifidus (LM) activation through the measurement of muscle thickness at the level of L5-L4 vertebrae, during rest and lower-extremity movement. Each participant will self-rate the pain intensity in the lumbar spine according to the Numeric Pain Rating Scale (NPRS). The pressure-pain threshold (PPT) will be measured using an algometer. Lumbar ROM will be measured using a dual inclinometer method in flexion and extension. The results will be compared between the intervention and control groups through mixed analysis of variance for LM thickness, lumbar ROM, PPT, and NPRS.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
40
central postroanterion mobilization on the most painful vertebral level at the lumbar spine
manual therapy
instrumental manual therapy
Imam Abdulrahman Bin Faisal University
Khobar, Eastern Province, Saudi Arabia
RECRUITINGNumeric pain rating scale
a series of numbers from 0 to 10, with '0' indicating no pain and '10' indicating the most intense pain possible
Time frame: 2-3 weeks
Lumbar Multifidus muscle activation
muscle activation quantified by measuring the muscle thickness during rest and activation positions.
Time frame: 2-3 weeks
Pressure pain threshold
measured at the most painful site on the back as well as on a mid-point at RT tibialis anterior muscle belly lateral to the tibia
Time frame: 2-3 weeks
Lumbar spine ROM
measured in flexion, extension, and lateral flexion to both sides. Dual inclinometer method used to take the measurements (Baseline Bubble Inclinometer device)
Time frame: 2-3 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.