Actively Recruiting

Phase Not Applicable
Age: 20Years - 50Years
All Genders
ID07632612

Comparing the Effectiveness of Tensioner Vs Slider Neurodynamic Techniques in Patients With Sciatica: A Randomised Control Trial

Led by Ibadat International University, Islamabad · Updated on 2026-06-08

80

Participants Needed

1

Research Sites

1 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating two neurodynamic approaches, tensioner and slider techniques, to treat patients with sciatica. This randomized controlled trial aims to determine which method is more effective in reducing pain intensity, improving functional disability, and enhancing mobility. The study is designed to help physical therapists choose the best neurodynamic therapy for patients suffering from sciatica. Participants will be randomly assigned to one of two groups. One group will receive slider neurodynamic mobilization combined with conventional physiotherapy, while the other group will receive tensioner neurodynamic mobilization along with conventional physiotherapy. Both treatments focus on neurodynamic mobilization techniques to address neurological issues related to sciatica. During the 8-week study period, researchers will assess pain intensity and functional disability from baseline to week 8 as primary outcomes. Secondary outcomes include measuring hip range of motion and lumbar flexion range of motion over the same timeframe. Participants will undergo evaluations related to their symptoms and physical function to monitor progress and treatment effects throughout the trial.

CONDITIONS

Brief Title

Comparing the Effectiveness of Tensioner Vs Slider Neurodynamic Techniques in Patients With Sciatica

Who Can Participate

Age: 20Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with radicular pain persisting for 12 weeks to 1 year, with no acute episode in the last 4 weeks
  • Unilateral symptoms radiating below the buttock to thigh, knee, or lower leg
  • Positive Slump Test
  • Positive Straight Leg Raise (SLR) test above 456
  • Functional limitation during activities such as walking or lifting
Not Eligible

You will not qualify if you...

  • BMI less than 20 kg/m8 or greater than 30 kg/m8
  • Previous history of spinal surgery
  • Presence of red flags such as significant motor or sensory loss, altered reflexes, or bowel/bladder dysfunction
  • Peripheral neuropathy
  • History of vertebral fracture or significant spinal or limb trauma
  • Systemic diseases like diabetes mellitus, cardiovascular, or renal disease
  • Progressive neurological deficits including motor weakness, sensory loss, or reflex changes
  • Pregnancy

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 8 weeks

Participants receive either slider or tensioner neurodynamic mobilization techniques along with conventional physiotherapy management to alleviate pain and improve function.

Weekly visits for up to 8 weeks

Trial Site Locations

Total: 1 location

1

Ibadat International Hospital

Rawalpindi, Punjab Province, Pakistan

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Research Team

S

Sojla Bashir, DPT, MSPT MSK

S

Sidra Hanif, DPT, MSNMPT, PhD PT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Frequently Asked Questions

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