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A study between the effects of Thoracic mobilization and neural mobilization on pain, range of motion and function in patients having low back pain with radiation to lower limb

Comparison between Thoracic Mobilization and Neural Mobilization on Pain, Range of motion and Function in Lumbar Radiculopathy: A randomized clinical trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070911
Enrollment
32
Registered
2024-07-19
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: M541- Radiculopathy

Interventions

Intervention1: Thoracic Mobilization: All the patient in this group will be treated by Thoracic Mobilization along with Moist Hot Pack, Supervised Exercises and HEP. Treatment will be given with 30 os

Sponsors

Chanchal Sah
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Both male and female patients. 2.Patients age between 35 and 60 years.[2] 3.Patients complaining of Low Back Pain radiating to posterior leg in unilateral limb. 4.Pain duration of more than 3 months. 5.Pain intensity according to Visual Analogue Scale (VAS) 3cm to 8cm. 6.Any two of the following special tests should be positive: a.Slump Test b.Straight leg raising test (Sciatic nerve bias) c.Sitting Root Test

Exclusion criteria

Exclusion criteria: 1.Musculoskeletal disorders like Fibromyalgia, Piriformis syndrome, history of fracture/surgery of spine or lower limb etc. 2.Red flag signs such as diagnosed cases of carcinoma, tumor, and infectious disease of spine like Tuberculosis etc. 3.Rheumatological disorders like Ankylosing spondylitis, Rheumatoid arthritis etc. 4.Neurological disorders like Cerebro-Vascular Accident, Spinal cord injury, any neurological deficit etc and congenital pathology such as Scoliosis, Spina Bifida etc. 5.Pregnancy. 6.Non-cooperative patients. 7.Sensory deficit/ Anaesthesia in back region.

Design outcomes

Primary

MeasureTime frame
1.Pain by VAS 2.ROM by MMST 3.Function by ODI Timepoint: 2 times - Before intervention and after 10th session of intervention

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactChanchal Sah

National Institute For Locomotor Disabilities(Divyangjan)

ptranth@gmail.com9874540980

Outcome results

None listed

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