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Clinical Trials/CTRI/2024/12/077744
CTRI/2024/12/077744
Recruiting
Not Applicable

Comparison between Myofascial Release versus Instrument Assisted Soft Tissue Mobilization (IASTM) in reducing pain, improving muscle strength and function with mechanical low back pain: An Experimental Study

Department of Physiotherapy School of Allied Health Sciences Galgotias University1 site in 1 country50 target enrollmentStarted: December 21, 2024Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Sponsor
Department of Physiotherapy School of Allied Health Sciences Galgotias University
Enrollment
50
Locations
1
Primary Endpoint
Numeric Pain Rating Scale

Overview

Brief Summary

  1. Mechanical low back pain is a prevalent condition affecting millions worldwide.

  2. Current treatments have varying degrees of effectiveness, and there is a need for

evidence-based alternatives.

  1. MFR and IASTM are popular manual therapies, but their comparative effectiveness is

unknown.

  1. Limited research exists comparing MFR and IASTM for mechanical low back pain.

A research study comparing Myofascial Release and Instrument Assisted Soft Tissue

Mobilization is necessary because it would address a significant gap in the literature,

providing clinicians with evidence-based insights on the most effective treatment strategies for

managing mechanical low back pain. By exploring pain reduction, muscle strength, and

functional improvement, such a study has the potential to improve patient care, reduce

disability, and influence healthcare policy surrounding the treatment of low back pain.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Participant, Investigator and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 45.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Age: 18-45 years
  • Diagnosis of mechanical low back pain (MLBP)
  • Pain duration: ≥ 6 weeks
  • Pain intensity: ≥ 3/10 on the Numeric Pain Rating Scale (NPRS)
  • Ability to provide informed consent.

Exclusion Criteria

  • Previous spinal surgery or instrumentation
  • Severe spinal degeneration or deformity
  • Spinal fracture or tumor
  • Neurological deficits (e.g., numbness, tingling, weakness)
  • Pregnancy or breastfeeding
  • Recent trauma or injury to the lower back
  • Contraindications to manual therapy (e.g., bleeding disorders, osteoporosis).

Outcomes

Primary Outcomes

Numeric Pain Rating Scale

Time Frame: 0 Week | 4 Week

Back Muscles strength measurement through sphygmomanometer

Time Frame: 0 Week | 4 Week

Secondary Outcomes

  • Oswestry Low Back Pain Disability(baseline- 4 weeks)

Investigators

Sponsor
Department of Physiotherapy School of Allied Health Sciences Galgotias University
Sponsor Class
Other [university]
Responsible Party
Principal Investigator
Principal Investigator

Dr Chandan Kumar

Department of Physiotherapy, Galgotias University

Study Sites (1)

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