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Comparative Effects of Dynamic Stretching Versus Slider Neurodynamic Technique In Patients With Lumbar Radiculopathy

Comparative Effectiveness of Dynamic Stretching Versus Slider Neurodynamic Technique In Patients With Lumbar Radiculopathy : a Randomised Controlled Trail

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07384832
Enrollment
72
Registered
2026-02-03
Start date
2025-06-20
Completion date
2026-02-10
Last updated
2026-03-06

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, sciatica

Brief summary

This study will be a randomised clinical trial conducted at the University of Lahore Teaching Hospital, Lahore, Pakistan. A total of 72 participants will be selected and randomly allocated into two treatment groups (36 participants in each group) using the lottery method. All screened and willing participants who meet the eligibility criteria will be assigned to either Group A or Group B. Group A will receive dynamic stretching along with routine physiotherapy. Routine physiotherapy will include TENS (15 minutes), hot moist pack (10 minutes), soft tissue mobilisation (5-7 minutes), abdominal bracing, pelvic tilt, and alternate leg extension exercises. The dynamic stretching part will include the slump stretch, cat-camel stretch, hamstring sweeps, child pose stretch, and overhead lateral stretch. Each stretch will be performed in 2 sets of 15-20 repetitions with 1-minute rest between sets. Treatment will be provided four times per week for 6 weeks. Group B will receive slider neurodynamic mobilisation along with the same routine physiotherapy protocol as group A. Slider neurodynamic mobilisation will be performed in the slump position, sitting at the edge of the plinth with the thighs parallel to each other and arms crossing behind the back. The examiner asked the patient to move actively and conversely from a position of neck and trunk flexion, knee flexion, and plantar flexion, to a position of neck and trunk extension, knee extension, and ankle dorsiflexion with 3 sets of 1-minute sliders and 1-minute rest between sets. Treatment will be provided four times per week for 6 weeks. All participants will undergo assessments at baseline, at the end of the 3rd week, and at the end of the 6th week.

Detailed description

* Screening Participants who meet the inclusion criteria was recruited using a convenience sampling technique. This involves selecting participants who are readily available to participate in the study. * Allocation Eligible participants were screened and informed about the study, including its purpose, procedures, potential risks, and benefits. Informed consent was obtained from each participant prior to their formal enrollment in the study. * Randomization: Following the baseline assessment, the randomization was conducted using the Online Randomizer tool (https://www.randomizer.org/). By specifying the group numbers, the number of participants per group, and the total number of participants, unique identification numbers were generated for each participant. • Blindness: This study was single-blinded; the patients were kept blinded about the study and were not informed about the exercise protocol they received. • Intervention After taking consent, participants was selected based on the inclusion criteria. Sample of 72 was then be randomly divided into two groups. All participants received a 35-minute treatment session, 4 days per week for 6 weeks, consisting of 15 minutes of routine physiotherapy and 20 minutes of a specific intervention: Group A (Dynamic Stretching): Routine physiotherapy included TENS (70 Hz, 100 microseconds) for 15 minutes, hot moist packs for 10 minutes, and core strengthening (pelvic tilts and leg extensions). The main intervention was 20 minutes of dynamic stretching, including the slump stretch(The patient performed a slump stretch, seated with knees bent, extending one leg at a time while flexing the trunk forward to stretch the lumbar nerve roots), cat and camel(The patient alternated between spinal flexion and extension while on hands and knees.), hamstring sweeps(The patient performed dynamic hamstring stretches, sweeping the leg forward and back to increase flexibility in the posterior chain.), child's pose, and overhead lateral stretches(The patient performed a side stretch to target the quadratus lumborum and obliques, releasing tension from the side of the back.). Each exercise was performed for 4 minutes in 2 sets of 10-15 repetitions with 1 minute rest interval. Group B (Slider Neurodynamic Technique): Routine physiotherapy matched Group A but included 5 minutes of soft tissue mobilization. The main intervention was the Slider Neurodynamic Mobilization (NDM). Patients were seated and performed rhythmic movements: moving from neck/trunk flexion and knee flexion to neck/trunk extension and knee extension. This movement is designed to "slide" the nerve through the spinal canal without over-tensioning it. This was performed in 3 sets of 1-minute intervals. Clinical assessments for pain (NPRS), disability (MODI), and flexibility (MMST) were recorded at baseline, the 3rd week, and the 6th week to compare the efficacy of the two protocols.

Interventions

Dynamic stretching protocol will include: * Slump Stretch (4 minutes): The patient performed a slump stretch, seated with knees bent, extending one leg at a time while flexing the trunk forward to stretch the lumbar nerve roots. * Cat and Camel Stretch (4 minutes): The patient alternated between spinal flexion and extension while on hands and knees. * Hamstring Sweeps (4 minutes): The patient performed dynamic hamstring stretches, sweeping the leg forward and back to increase flexibility in the posterior chain. * Child's Pose Stretch (4 minutes): The patient performed a child's pose stretch to improve flexibility in the lower back and hips. * Overhead Lateral Stretch (4 minutes): The patient performed a side stretch to target the quadratus lumborum and obliques, releasing tension from the side of the back. Each dynamic stretch will be performed as follows: * 2 sets of 10-15 repetitions * 1-minute rest between sets * Performed 3 sessions/week for 6 weeks

OTHERslider neurodynamic mobilization

Performed in the slump sitting position. Participants move from neck and trunk flexion with knee flexion and plantar flexion toward neck and trunk extension with knee extension and ankle dorsiflexion. The protocol consists of 3 sets of 1-minute slider movements, each followed by 1 minute of rest.

TENS: Conventional Transcutaneous Electrical Nerve Stimulation was applied for 15 minutes (70 Hz frequency, 100 μs pulse width). Two 40×40 mm electrodes were positioned in a crossed pattern bilaterally over the lumbosacral region. A hot moist pack was applied to the lumbosacral and gluteal regions for 10 minutes in prone lying.Strengthening and Stabilization Exercises: Pelvic tilts were performed in crook-lying with 10-15 second holds. Alternate leg extensions were performed in prone with 10-second holds. Quadriceps and hip adductor/abductor strengthening were completed using isometric contractions (e.g., pillow squeeze). Core stabilization exercises included gluteal bridge, abdominal crunch, and cross-crawl exercises.Exercise selection was symptom-guided: Flexion-biased or Extension-biased.All exercises were performed in 2 sets of 15-20 repetitions with 1 min rest. and lumbar traction.

Sponsors

University of Lahore
Lead SponsorOTHER
University of Lahore Hospital (ULH)
CollaboratorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

This study used a single-blind approach. This means that while the researchers knew which treatment each person was getting, the patients did not know if they were in the "Dynamic Stretching" group or the "Slider Neurodynamic" group. They were not told which exercise protocol was the main focus of the study or which one was expected to be more effective. This helps ensure that the patients' expectations did not influence the results or their reporting of pain levels.

Eligibility

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

Inclusion criteria

\- • Participants aged between 25 - 50 years of both genders are included * Symptoms that radiate below the buttocks, thigh/ knee, and lower leg for more than 4 weeks. * A minimum baseline Pain intensity (NPRS) \>4/10. (Morsi et al., 2022) * Diagnosis of discogenic low back pain (LBP) confirmed by MRI ( disc bulge, protrusion, and herniation) and referred by an orthopedic physician. * LBP due to muscle tightness/ or nerve compression. * Had a positive slump test with reproduction of neurological symptoms, and had functional disabilities in certain daily tasks as lifting or walking.

Exclusion criteria

* Patients with lumbar spondylolisthesis. * Currently pregnant women or in the early post-partum period. * Patients with autoimmune disease (ankylosing spondylitis, RA) * Previous history of trauma ( fracture, soft tissue injuries) or spinal surgery (spinal laminectomy). * Systemic diseases like cardiovascular disease( unstable angina, uncontrolled cardiac arrhythmias) and metabolic diseases. * Contraindication to exercises or usage of TENS (cardiac pacemaker, skin allergies to electrodes).

Design outcomes

Primary

MeasureTime frameDescription
Pain Intensity (NPRS)baseline, 3rd week, 6th weekPain Intensity will n=be measured using the numeric pain rating scale (NPRS) , where participants rate their pain on a scale from 0 to 10 (0= no pain, 10= worst possible pain). the scale will be used to assess changes in pain levels over the duration of the intervention.

Secondary

MeasureTime frameDescription
Functional Disability (Modified Oswestry Disability Index -MODI)baseline,3rd week, 6th weekFunctional disability will be measured using the modified oswestry low back pain disability index, a validated questionnaire assessing limitations in everyday activities. scores range from 0-100 % with higher scores indicating greater disability. the measure will be used to determine changes in functional ability.
Lumbar Flexion Range of Motion (Modified-Modified Schober Test - MMST)baseline, 3rd week, 6th weekLumbar flexion range of motion will be assessed using the Modified-Modified Schober Test (MMST). The test measures the change in distance between two points on the lumbar spine during forward flexion. Increased distance indicates improved lumbar mobility.

Countries

Pakistan

Contacts

PRINCIPAL_INVESTIGATORAsim Arif, PhD

University of Lahore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026