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Effect of wearing lumbosacral belt for different duration in lumbar disc herniation patients

Impact of Varying Durations of Lumbosacral Belt Wear-Time on Pain Perception, Core Stability and Functional Disability in individuals with Chronic Lumbar Disc Herniation - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110757
Enrollment
54
Registered
2026-05-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention1: Group 1 (Whole Day LS Belt Group): Wear LS Belt for minimum 8 hours daily except during sleep + Moist Hot Pack, Transcutaneous Electrical Nerve Stimulation(TENS), Core Strengthening Ex

Sponsors

Reepakshi Loria
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Age 20-50 years. 2) Clinically and MRI confirmed chronic Lumbar Disc Herniation (only disc bulge will be included). 3) Willingness to wear the Lumbosacral Belt as instructed and attend all assessments. 4) Ability to understand the study procedures and provide informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients with disc protrusion/extrusion/sequestration will be excluded from this study. 2) Cauda Equina Syndrome or urgent surgical indications. 3) Prior lumbar spine surgery at the affected level. 4) Spinal infection, tumor, inflammatory spinal disorders, or primary lumbar spinal stenosis. 5) Current or recent use of a lumbar belt or structured lumbar physiotherapy. 6) Neuromuscular disorders affecting trunk muscle function. 7) Skin conditions preventing safe belt use. 8) Pregnancy or breastfeeding. 9) Metabolic disorders or severe uncontrolled medical conditions. 10) Cognitive impairment, language barriers, or inability to follow instructions.

Design outcomes

Primary

MeasureTime frame
Short-Form McGill Pain Questionnaire,Pressure Biofeedback,Oswestry Disability IndexTimepoint: Pre-Intervention (just after recruitment) Post-Intervention (after 12 sessions)

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactSandeep Pattnaik

Maharishi Markandeshwar Institute of Physiotherapy and Rehabilitation(MMIPR), Mullana, Ambala

physiosandeep94@gmail.com9348096886

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026