Health Condition 1: M999- Biomechanical lesion, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.The study will include patients aged 18 to 65 years diagnosed with chronic non-specific low back pain, defined as pain in the back, located between the last rib and the gluteal fold, with mechanical characteristics lasting more than 3 months. 2 Patients with Self-rated pain with an intensity of >20 mm on the visual analogue scale for pain will be included in the study. 3. Patients with mild VAS score = 3.4 cm corresponds best with mild pain and moderate VAS score 3.5 to 7.4 cm with moderate pain will be included in the study. 4. Patients with a score of 14% or more on the Oswestry Disability Index (ODI), Independently mobile (with or without aids) to be capable of participating in a rehabilitation programme,will be included in the study.
Exclusion criteria
Exclusion criteria: 1.Patients having primary pain area other than the lower back (from T12 to buttocks), leg pain as the primary problem (eg, nerve root compression or disc prolapse with true radicular pain/radiculopathy, lateral recess or central spinal stenosis)will be excluded. 2.Patients having Lumbar spine, lower limb or abdominal surgery in previous 6 months will be excluded. 3.Patients Having undergone pain-relieving procedures such as injection-based therapy (eg, epidurals) and day care procedures (eg, rhizotomy) in the last 3months will be excluded. 4.Patients with Pregnancy, rheumatological/inflammatory disease (eg, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, lupus erythematosus, Scheuermann’s disease). Progressive neurological disease (eg, multiple sclerosis, Parkinson’s disease, motor neuron disease)will be excluded. 5.Patients with Scoliosis and any other spinal deformity will be excluded. 6.Patients with inadequate English/Marathi language knowledge to complete outcome measures will be excluded. 7.Patients with Unstable cardiac conditions, red flag disorders like malignancy/cancer will be excluded. 8.Patients with Acute trauma such as fracture in the last 6months or infection, or spinal cord compression/cauda equina syndrome will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Disability Back extensor endurance Forward flexion & extension rangeTimepoint: 4 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| N/ATimepoint: N/A | — |
Countries
India
Contacts
DVVPF College of Physiotherapy