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Effectiveness of IASTM versus Myofascial Release on Pain and Thoracolumbar Fascia in Mechanical Low Back Pain

Effectiveness of Instrument-assisted Soft-tissue mobilization versus Myofascial release on Pain and Morphological characteristics of thoracolumbar fascia in Mechanical low back pain - NIL

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091089
Enrollment
112
Registered
2025-07-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: Instrument Assisted Soft Tissue Mobilization: Area: Thoracolumbar region (T12 to L5). Duration: ~5 10 minutes/session. Frequency: Single sessions per week for 4 weeks. Tools: Stainless

Sponsors

Dr Ehsanur Rahman
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults between 18 and 65 years Mechanical LBP of over 3 months duration with at least of days with pain over the prior 6-months (Deyo et al., 2014) Able to understand study procedures and willing to sign an informed consent document Willing to forgo any manual therapy treatment for LBP for the initial 4-week study period Willing to forgo any manual therapy treatment for LBP, other than study treatments, during the 4-week treatment period

Exclusion criteria

Exclusion criteria: Chiropractic care or other manual therapy treatment within 90 days Necessary tissue layers could not be visualized with ultrasound imaging Body Weight above 350 lbs. (158.76 kg), (safety limit for motorized table) Unable to tolerate or safely receive study procedures Condition identified requiring referral to another provider (e.g., suspected or confirmed abdominal aortic aneurysm, low back pain from suspected renal lithiasis) Unable or unwilling to comply with study procedures Current or planned pregnancy (self-reported) within the Study timeframe Prior surgery to the thoracolumbar region Needing a proxy Connective tissue disorder such as Marfan and Ehlers-Danlos syndrome

Design outcomes

Primary

MeasureTime frame
Ultrasound imaging for comparing the morphological characteristics Timepoint: 4 weeks

Secondary

MeasureTime frame
Numeric Pain Rating Scale (11-point) Pressure Pain Threshold (PPT) Oswestry Disability Index (ODI) Roland-Morris Disability Questionnaire (RMDQ) Timepoint: 4 weeks

Countries

Bangladesh

Contacts

Public ContactDr K M Amran Hossain

Jashore University of Science and Technology

kma.hossain@just.edu.bd8801735661492

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026