Foundation University College of Physical Therapy
Islamabad, Punjab Province, 46000, Pakistan
Location status: Recruiting
NCT Number: NCT07328282
This study examines the comparative effects of ELDOA and Spinal Mobilization with Leg Movement (SMWLM) on lumbar radiculopathy
Interested in participating?
Request Info30 year–50 year
All sexes
Interventional
Not applicable
Islamabad, Punjab Province, 46000, Pakistan
Location status: Recruiting
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
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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)
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.
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.
Time frame: baseline, 2nd and 4th week
Measured by Oswestry Disability Index, a 10-item questionnaire with six response options per item.
Time frame: baseline, 2nd week, 4th week
Pain severity will be measured using the Visual Analog Scale ranging from 0 (no pain) to 10 (worst imaginable pain).
Time frame: baseline, 2nd and 4th week
Lumbar spine range of motion will be assessed using a bubble inclinometer.
Contact information is provided by the study sponsor or research team.
Foundation University Islamabad
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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