Conservative management of low back pain using spine biofeedback device

To assess the clinical and functional outcomes following conservative management of mechanical low back pain with active structured rehabilitation program using spine biofeedback device - NIL

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/06/069282

Enrollment

Registered

2024-06-20

Start date

Unknown

Completion date

Unknown

Last updated

2024-06-24

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

Conditions

Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

Intervention1: Spine biofeedback device: Spine rehabilitation in sub-acute and chronic mechanical low back pain using spine biofeedback device for 12 weeks Control Intervention1: Not applicable: Study

Eligibility

Inclusion criteria

Inclusion criteria: Subacute and chronic mechanical low back pain

Exclusion criteria

Exclusion criteria: Pregnancy, Vertebral compression fracture, severe progressive neurologic deficit including cauda equina syndrome, spinal infection, spinal neoplasm, inflammatory spondyloarthritis, previous spine surgery and unwillingness due to any reason

Design outcomes

Primary

Measure	Time frame
Pain severity as per VAS score Disability as per ODI Trunk range of motion and strengthTimepoint: At baseline and 12 weeks post rehabilitation	—

Secondary

Measure	Time frame
Isolated trunk ROM & strength in patients with mechanical low back pain on first visit & comparison with normal ROM & strength in normal adultsTimepoint: Baseline at first visit	—

Countries

India

Contacts

Public ContactAmir Khan

Armed Forces Medical College

surajbansal.ortho@gmail.com8411072219

Outcome results

None listed

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