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RecruitingNCT07887685Updated Oct 21, 2026

Comparative Effect Between Mulligan Leg Raise and Spinal Mobilization With Limb Movement in Lumbar Radiculopathy

An interventional study of Mulligan Leg Raise traction and Spinal Mobilization with Limb Movement - SMWLM in Lumbar Radiculopathy, sponsored by Foundation University Islamabad. Recruiting at 1 site in Pakistan. Open to participants aged 30 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-10-21.

Sponsored by Foundation University Islamabad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2026; still recruiting 1 month later.
Updated Oct 21, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
30 Years to 50 Years
Sex
All
01

Study summary

This study examines the comparative effects of mulligan leg raise traction and Spinal Mobilization with Leg Movement (SMWLM) on lumbar radiculopathy

Read the detailed description

Participants were randomly assigned into two groups:

Group A, which recieved leg raise traction 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 VAS, ODI, and bubble inclinometer

02

Conditions studied

  • Lumbar Radiculopathy

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03

In context

Radiculopathy

498 studies on the registry are indexed under Radiculopathy; 144 are open to participants now.

This study's planned enrollment of 44 is below the median of 60 across 385 interventional studies indexed under Radiculopathy.

Browse Radiculopathy studies →

Lead sponsor

Foundation University Islamabad is the lead sponsor of 253 studies on the registry; 140 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

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 crossed SLR test positive Slump test positive pain and symptoms distribution in dermatomal pattern of L4 and L5

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

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
44 participants (estimated)

Study arms

  • Experimental
    Group A mulligan leg raise traction

    Group A will receive standard treatment of ELDOA Strengthening will be divided into following phases 1. Warm up phase: 2. Strengthening phase: 3. Cool down phase

    Procedure: Mulligan Leg Raise traction

  • Experimental
    Spinal moblization with limb movement

    Group B will receive Standard treatment of spinal mobilzation and limb movement Strengthening will be divided into following phases 1. Warm up phase: 2. Strengthening phase: 3. Cool down phase:

    Procedure: Spinal Mobilization with Limb Movement - SMWLM

Interventions

  • ProcedureMulligan Leg Raise traction

    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. and Participants will receive straight leg raise traction.

  • 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. and Participants will receive spinal mobilization combined with limb movement along with standard physiotherapy. The technique will be repeated three times.

06

What researchers measure

Primary outcomes

  1. Lumbar Pain Intensity

    Pain severity will be measured using the Visual Analog Scale ranging from 0 (no pain) to 10 (worst imaginable pain).

    Time frame: Baseline, 2nd week, and 4th week

  2. Functional Disability

    Measured by Oswestry Disability Index, a 10-item questionnaire with six response options per item.

    Time frame: Baseline, 2nd week, and 4th week

  3. Lumbar Range of Motion

    Lumbar spine ROM will be assessed using a universal inclinometer.

    Time frame: Baseline, 2nd week, and 4th week

07

Study locations

1 of 1 sites recruiting
  • Foundation University College of Physical Therapy
    Islamabad, Punjab Province 44000, Pakistan
    Recruiting
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 21, 2026
Show all 1 update
  1. Oct 21, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07887685
Responsible party
Sponsor
First posted
Oct 21, 2026
Start date
Sep 23, 2026
Primary completion
Jan 1, 2027 (estimated)
Completion
Jan 15, 2027 (estimated)
Last update
Oct 21, 2026

Study contacts

Maham Farooq, DPT
Contact
mahamfarooq813@gmail.com
0304 8132250
Ruqia Begum, MS-OMPT
Contact
ruqia@fui.edu.pk
+92 311 5532544

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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