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Surface Electromyography in Stratifying Chronic Low Back Pain.

Completed
Conditions
Low Back Pain
Interventions
Procedure: Surface Electromyography
Registration Number
NCT04960358
Lead Sponsor
University of Malaya
Brief Summary

Surface Electromyography can be utilised to detect normal muscle electrical activity during maximum forward flexion termed Flexion Relaxation Response (FRR)

Detailed Description

In this study, our primary objective is to assess FRR and disability (ODI) correlation protocol as an objective tool in stratifying Chronic LBP. We also would like to evaluate the relationship between FRR with pain intensity and lumbar range of motion as our secondary objective.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Participants aged between 20 - 70 years old
  • Mechanical LBP > 6 weeks (not acute LBP)
  • Not received any specific exercise spinal manipulation or surgery to improve LBP within the last 3 months.
Exclusion Criteria
  • Pregnancy
  • Radicular LBP patients or specific-spinal pathology / "red-flags".
  • Surgical intervention for the current LBP complaint (includes traumatic causes of LBP with surgical intervention)
  • Cognitive or communication difficulty preventing active participation in exercises or communicating pain scores

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Chronic LBPSurface ElectromyographyWill be applied Surface Electromyography
Primary Outcome Measures
NameTimeMethod
Flexion Relaxation Response (FRR) ratio1 YEAR

The FRR ratio was calculated from the best SEMG values obtained during Forward Lumbar Flexion \& Extension

Oswestry Low Back Pain Disability Questionnaire1 YEAR

Questionnaire of the functional assessment for the low back pain patient

Secondary Outcome Measures
NameTimeMethod
Gross Range of Motion1 YEAR

Degree of trunk motion at maximum voluntary flexion, measured by inclinometer at the level of T12

Visual Analog Scale1 YEAR

Representing range of pain intensity from no pain on the far left to most intense pain on the far right.

Trial Locations

Locations (1)

University Malaya Medical Centre

🇲🇾

Kuala Lumpur, Malaysia

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