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Comparative Effects Between ELDOA and Spinal Mobilization With Limb Movement in Lumbar Radiculopathy

Comparative Effects Between ELDOA and Spinal Mobilization With Limb Movement in Lumbar Radiculopathy

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07328282
Enrollment
36
Registered
2026-01-09
Start date
2025-06-01
Completion date
2026-01-15
Last updated
2026-01-09

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

Conditions

Lumbar Radiculopathy

Keywords

Lumbar Radiculopathy, lumbar pain

Brief summary

This study examines the comparative effects of ELDOA and Spinal Mobilization with Leg Movement (SMWLM) on lumbar radiculopathy

Detailed description

Participants were randomly assigned into two groups: Group A, which performed structured ELDOA exercises targeting spinal decompression and postural alignment Group B, which received SMWLM interventions focusing on spinal mobilization combined with controlled leg movements. Pain, functional disability, and lumbar range of motion were measured using Visual Analog Scale, Oswestry Disability Index, and bubble inclinometer

Interventions

PROCEDUREELDOA

Participants will receive a four-week physiotherapy program with three sessions per week. Each session will heat application followed by supervised stretching and strengthening exercises. Participants in Group A will receive ELDOA in addition to standard physiotherapy. Each position will be sustained for at least one minute, with gradual progression to the full posture as flexibility and control improve.

PROCEDURESpinal Mobilization with Limb Movement - SMWLM

Participants will receive a four-week physiotherapy program with three sessions per week. Each session will heat application followed by supervised stretching and strengthening exercises. Participants in Group B will receive spinal mobilization combined with limb movement along with standard physiotherapy. The technique will be repeated three times.

Sponsors

Foundation University Islamabad
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Randomized control trial

Eligibility

Sex/Gender
ALL
Age
30 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Age 30 -50 years * both male and female * Unilateral lumbar radiculopathy * Posteriolateral mild disc herniation on MRI * SLR test positive (30 to 70) degree * crosed SLR test positive * Slump test positive * pain and symptoms disturbution in dermatomal pattern of L4 and L5

Exclusion criteria

* MRI findings indicating i. Spinal instability ii. Significant neuroforaminal stenosis iii. Structural abnormalities requiring surgical intervention (e.g., large disc herniation ) * Clinical findings indicating: i. Absence of severe neurological and severe motor weakness (Manual Muscle Testing grades 0, 1, or 2) ii. Signs of cauda equina lesion (e.g., saddle anesthesia, bowel/bladder dysfunction) * Diagnosed spinal conditions i. Lumbar spondylolisthesis ii. Lumbar spine fracture iii. Spinal stenosis iv. Spinal tumor v. Ankylosing spondylitis * History of previous spinal surgery Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Functional Disabilitybaseline, 2nd and 4th weekMeasured by Oswestry Disability Index, a 10-item questionnaire with six response options per item.
Pain Intensitybaseline, 2nd week, 4th weekPain severity will be measured using the Visual Analog Scale ranging from 0 (no pain) to 10 (worst imaginable pain).
Lumbar Range of Motionbaseline, 2nd and 4th weekLumbar spine range of motion will be assessed using a bubble inclinometer.

Countries

Pakistan

Contacts

Primary ContactUzma Jabeen
jaeenuzma358@gmail.com0341-3737439

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026