- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05258214
Mulligan BLR Versus Mulligan TSLR Versus Neural Mobilization n Patient With Lumber Radiculopathy
Mulligan Bent Leg Raise Versus Mulligan Traction Straight Leg Raise Versus Neural Mobilization With Conventional Therapy On Pain & Functional Disability In Patient With Lumber Radiculopathy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Faisalabad, Punjab, Pakistan, 38000
- Ripah International university
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Between the ages of 18 and 65, all genders
- positive slump measure of lumbar specific nerve bias,
- mild to moderate irritation on a Numeric Pain Level Scale of less than seven,
- unilateral radiculopathy in the distribution of a single nerve with a favourable SLR,
- prone knee bent test; positve test,
- hypoaesthesia in a specific dermatome of the unilateral lower limb, accompanied by reduced mobility
- the result of the deep tendon (knee jerk, ankle jerk).
Exclusion Criteria:
- individuals with gradually occurring neurological problems
- Trauma, cancer, and constitutional symptoms are indeed red flags (Fever, Malaise, Weight Loss).
- Hip and knee fractures are common.
- Lower-extremity dislocations.
- Hamstring strains.
- Joint hypermobility of the lower limb.
- Muscle imbalance in lower limb
- Nerve lesions in the lower extremity.
- Subjects who have had low back pain in the previous two months.
- Hip flexion ROM was greater than 100 degrees for the straight knee.
- Neurological defects.
- Metal bolts, plates, or screws in the femur.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Mulligan Bent Leg Raise With Conventional Therapy
This group will receive mulligan's bent leg raise with conventional therapy. In a mulligan bent leg lift, the practitioner stands on the side of the supine subject on the couch with minimal hamstring stability. The subject's flexed knee is placed over the therapist's shoulder, and the subject is instructed to force the therapist with his leg before relaxing. At this moment, the therapist pushes subject's bent knee as high as possible on the same side as his (therapist's) shoulder. Mulligan's Bent Leg is performed three times. The raises took 7 seconds to keep and 5 seconds to relax. And conventional therapy includes ultrasound, lumber strengthening, stretching exercises, stabilizing exercises for 30 minutes. |
Mulligan's bent leg raise, as well as the extreme Straight Leg Raise, can be used to relieve Low Back Pain.
It can be used to treat leg discomfort that is above the knee.
Bent Leg Raise methods are used where there is a restricted range of motion in the hip flexion joint, as well as low back pressure with or without referred leg pain.
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EXPERIMENTAL: Mulligan Traction Straight Leg Raise With Conventional Therapy
This group will receive mulligan's traction Straight Leg Raise with conventional therapy. Patients were placed in a supine position on a low couch or the floor and provided the Mulligan traction leg raise with knees bent.. Mulligan's Traction is repeated three times. Straight Leg Raise was kept for 7 seconds and then relaxed for 5 seconds. Three repetitions of the pain-free Straight Leg Raise traction is performed. And conventional therapy include ultrasound, lumber strengthening, stretching exercises, stabilizing exercises for 30 minutes. |
Mulligan traction leg raise exercises are a non-invasive treatment that has been shown to help people with low back pain and reduced hip flexion range.
Conservative sciatica therapy focuses on pain relief, but increasing Straight Leg Raise range will help restore normal mobility and reduce the severity of low back disability.
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EXPERIMENTAL: Neural Mobilization With Conventional Therapy
This group will receive neural mobilization with conventional therapy. Straight leg raise movements will be used to trigger sciatic nerve pain during neural mobilization exercises. Based on the participant's responses and tolerance, several repetitions may be done. The range of motion will be expanded as the symptom increases before the full Straight Leg Raise range is reached. The position will be kept for a total of 5 minutes and 30 seconds. Repetition will be carried out. And conventional therapy include ultrasound, lumber strengthening, stretching exercises, stabilizing exercises for 30 minutes. |
These techniques are designed to mobilize a nerve with as little pressure down, resulting in a larger longitudinal excursion than techniques that actually lengthen the nerve bed, such as tensioning procedures.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric pain rating scale
Time Frame: 12th Week
|
The Numerical Pain Rating Scale is a subjective measure in which individuals rate their pain on an eleven-point numerical scale.
The scale is composed of 0; no pain at all to 10; worst imaginable pain.
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12th Week
|
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Modified Oswestry low back pain questionnaire
Time Frame: 12th Week
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Modified Oswestry low back pain questionnaire is an extremely important tool that researchers and disability evaluators use to measure a patient's permanent functional disability.
The test is considered the 'gold standard' of low back functional outcome tools
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12th Week
|
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Goniometer
Time Frame: 12th Week
|
Goniometer has been the most widely used tool for measuring joint range of motion.
To ensure reliable measurement, standardized, specific positions and landmarks are used to measure each joint movement.
|
12th Week
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC-FSD-00272
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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