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Comparing The Effect Of Slider Neural Mobilization with KAAATSU Training in individuals with unilateral lumbar radiculopathy

Effect Of Slider Neural Mobilization With KAASTSU Training In Individuals With Unilateral Lumbar Radiculopathy- A Randomized Placebo Controlled Trail - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093491
Enrollment
36
Registered
2025-08-22
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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: Experimental Group: Slider Neural Mobilization with KAATSU Training In Unilateral Lumbar Radiculopathy: Experimental Group: Slider Neural Mobilization with KAATSU Training in Unilateral

Sponsors

KLE ACADEMY OF HIGHER EDUCATION AND RESEARCH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ?Participants: -All genders within the age group of 25-60 years. -Diagnosed with subacute or chronic-stage low back pain with unilateral radiculopathy involving the sciatic nerve and its branches. -Diagnosed with disc protrusion on MRI. -Pain intensity score minimum 3-7 on Numeric Pain Rating Scale (NPRS). -Willing to participate and who can comprehend the commands.

Exclusion criteria

Exclusion criteria: ?Participants: -Spinal or lower limb surgeries within the last year. -Inflammatory or other specific disorders of the spine, such as ankylosing spondylitis, Paget?s disease, vertebral collapse, rheumatoid arthritis, spondylolisthesis, and severe osteoporosis.1 -Red flags for neural mobilization, such as trauma, cancer, and infection, and pregnant women, fractures of the lower limb or spine within the past six months 4 -Red flags for blood flow restriction training, such as skin disorders like allergic conditions, open wounds, vascular disorders, and active infection. -Cardiopulmonary disorders like hypertension -Who cannot comprehend the commands.

Design outcomes

Primary

MeasureTime frame
Assessment of pain using NPRS, functional disability using MODQ, and ROM using a universal goniometerTimepoint: Assessment will be done pre treatment and at the end of 2nd week

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactPeeyoosha Gurudut

KAHER Institute of Physiotherapy Nehru nagar Belagavi, Karnataka

peeyooshagurudut@klekipt.edu.in9844821355

Outcome results

None listed

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