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The Effect of McKenzie Therapy on Lower Back Pain and Nerve Health

Effectiveness of Mechanical Diagnosis and Therapy on Disc Morphology and Neurophysiology in L5/S1 Lumbar Disc Herniation - NIL

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090649
Enrollment
60
Registered
2025-07-10
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: M439- Deforming dorsopathy, unspecified

Interventions

Intervention1: McKenzie (MDT) Exercises: Total duration: 4 weeks. Participants in this group will receive supervised Mechanical Diagnosis and Therapy (MDT), also known as McKenzie exercises. Each sess
2 3 sets of 10 15 repetitions, 10 15 minutes per session), and modalities including moist heat packs for 15 20 minutes (2 3 times daily) and TENS for 20 30 minutes (1 2 times daily). Ergonomic trainin

Sponsors

Dr Ehsanur Rahman
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults aged 25 to 55 years, both sexes. 2. Clinically diagnosed L5 to S1 lumbar disc herniation confirmed by MRI (disc protrusion or bulge, with or without nerve root compression). 3. Chronic low back pain with or without radiating leg pain, consistent with radiculopathy, for more than 6 weeks. 4. Pain intensity of 3 or above on the Visual Analogue Scale (VAS). 5. Inadequate response to prior conservative treatments (e.g., rest, oral medication, or physiotherapy without supervision). 6. Positive Straight Leg Raise test or neurological signs such as sensory change, weakness, or altered reflex. 7. Not currently recommended for surgery or prefers non-surgical treatment. 8. Provides written informed consent to participate.

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with calcified or hard disc herniation confirmed by MRI. 2. Symptoms indicating Cauda Equina Syndrome (e.g., urinary retention, saddle anaesthesia). 3. Presence of other spinal pathologies such as tumors, infections (e.g., tuberculosis), or vertebral fractures. 4. History of previous lumbar spine surgery at the affected level (L5/S1). 5. Participants with uncontrolled diabetes mellitus. 6. Pregnant women or those planning pregnancy during the study period. 7. Participants with medical contraindications to exercise, including bleeding disorders, active anticoagulant therapy (excluding low-dose aspirin), and severe cardiovascular or neuromuscular conditions.

Design outcomes

Primary

MeasureTime frame
1. Pain by VAS and PPTs 2. Disc Morphology by disc height, disc echogenicity, and disc displacement (assessed via MSK-USG) 3. Neurological Recovery by SLR, NCS, and EMGTimepoint: 4 weeks

Secondary

MeasureTime frame
Disability by Oswestry Disability Index (ODI)Timepoint: Baseline, 1 month, 3 months, and 6 months post-intervention

Countries

Bangladesh

Contacts

Public ContactDr Kazi Md Amran Hossain

Jashore University of Science and Technology

kma.hossain@just.edu.bd8801735661477

Outcome results

None listed

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