ClinicalTrials.gg
RecruitingNCT07632612Updated Jun 8, 2026

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

An interventional study of Slider Neurodynamic Technique Group and Tensioner Neurodynamic Technique Group in Sciatica and Sciatica Pain, sponsored by Ibadat International University, Islamabad. Recruiting at 1 site in Pakistan. Open to participants aged 20 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-06-08.

Sponsored by Ibadat International University, Islamabad · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
20 Years to 50 Years
Sex
All
01

Study summary

objective of this randomized controlled trial is to examine the efficacy of both tensioner and slider neurodynamic approaches in patients suffering from sciatica. This study seeks to establish which approach is more efficacious in alleviating pain intensity, disability functional, and mobility. The results of this study will assist physical therapists in making an informed decision on the type of neurodynamic therapy for their patients.

Read the detailed description

Due to the increasing prevalence of sciatica and evidence based treatment options using physiotherapy that offers effective alleviation of pain and rehabilitation of function. Neurodynamic mobilization focuses on addressing neurological problems; thus, there is a need to know about the effectiveness of the different types of the technique being used.

The current research is expected to contribute to the existing literature in the area of physiotherapy concerning the identification of the most effective neurodynamic technique in the case of sciatica. These findings could be helpful for medical practitioners during their work, making decisions and planning treatment. At the same time, the results of the investigation may become the basis for further research.

02

Conditions studied

  • Sciatica
  • Sciatica Pain

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03

In context

Sciatica

149 studies on the registry are indexed under Sciatica; 31 are open to participants now.

This study's planned enrollment of 80 is above the median of 68 across 122 interventional studies indexed under Sciatica.

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Lead sponsor

Ibadat International University, Islamabad is the lead sponsor of 53 studies on the registry; 36 are open to participants now.

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

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Who can participate

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

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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 45°
  • Functional limitation during activities such as walking or lifting

Exclusion criteria

Exclusion Criteria:

  • \< 20 kg/m² or > 30 kg/m²
  • Previous history of spinal surgery
  • Presence of red flags (significant motor/sensory loss, altered reflexes, or bowel/bladder dysfunction)
  • Peripheral neuropathy
  • History of vertebral fracture or significant spinal/limb trauma
  • Systemic diseases (e.g., diabetes mellitus, cardiovascular, or renal disease)
  • Progressive neurological deficits (motor weakness, sensory loss, reflex changes)
  • Pregnancy
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

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

Study arms

  • Experimental
    Slider Neurodynamic Technique Group

    Participants will receive slider neurodynamic mobilization techniques along with conventional physiotherapy management.

    Other: Slider Neurodynamic Technique Group

  • Active comparator
    Tensioner Neurodynamic Technique Group

    Participants will receive tensioner neurodynamic mobilization techniques along with conventional physiotherapy management.

    Other: Tensioner Neurodynamic Technique Group

Interventions

  • OtherSlider Neurodynamic Technique Group

    will receive slider neurodynamic mobilization techniques along with conventional physiotherapy management.

  • OtherTensioner Neurodynamic Technique Group

    will receive tensioner neurodynamic mobilization techniques along with conventional physiotherapy management.

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What researchers measure

Primary outcomes

  1. Pain intensity

    will be measured using VAS

    Time frame: Baseline to Week 8

  2. Functional disability

    measured using Oswestry Disability Index (ODI)

    Time frame: Baseline to week 8

Secondary outcomes

  1. Hip range of motion

    assessed using Goniometer

    Time frame: Baseline to week 8

  2. Lumbar flexion Range of Motion

    measured using Modified-Modified Schober Test (MMST)

    Time frame: Baseline to Week 8

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Study locations

1 of 1 sites recruiting
  • Ibadat International Hospital
    Rawalpindi, Punjab Province, Pakistan
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07632612
Lead sponsor
Ibadat International University, Islamabad
Responsible party
Sponsor
First posted
Jun 8, 2026
Start date
Jun 3, 2026 (estimated)
Primary completion
Sep 3, 2026 (estimated)
Completion
Sep 10, 2026 (estimated)
Last update
Jun 8, 2026

Study contacts

Sojla Bashir, DPT, MSPT MSK
Contact
sojlabashir@gmail.com
+923008580082
Sidra Hanif, DPT, MSNMPT, PhD PT
Contact
sidra.hanif@uipt.iiui.edu.pk
+923335985631

Oversight

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

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