NCT06947785

Brief Summary

This study will address to evaluate and compare both Neural mobilization and Manual Myofascial Release of piriformis and Lumbar muscles in sciatic pain with the aim of evaluating and identifying the most effective intervention for managing this specific condition, and provide valuable insights into the effectiveness, mechanisms, and practical considerations associated with these interventions, ultimately contributing to evidence based and patient centered care.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 7, 2025

Completed
8 days until next milestone

Study Start

First participant enrolled

April 15, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

April 27, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 3, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

April 8, 2026

Status Verified

April 1, 2026

Enrollment Period

6 months

First QC Date

April 7, 2025

Last Update Submit

April 2, 2026

Conditions

Keywords

Neural MobilizationMyofascial ReleaseSciatic Pain

Outcome Measures

Primary Outcomes (4)

  • Numerical pain rating scale

    A subjective pain assessment tool where patients rate their pain intensity on a scale from 0 (no pain) to 10 (worst imaginable pain).

    Four Weeks

  • Universal Goniometer

    Joint range of motion will be measured using a Universal Goniometer in degrees (°). Each joint movement will be assessed individually. The goniometer will be used following standardized procedures as per the American Academy of Orthopaedic Surgeons (AAOS) guidelines. Unit of Measure is degrees.

    Four Weeks

  • Patient-Specific Functional Scale

    The Patient-Specific Functional Scale is a validated patient-reported outcome measure used to assess functional limitations based on activities identified by the patient. Participants will rate their ability to perform 3-5 self-selected activities that are important to them, using an 11-point scale ranging from 0 to 10. Minimum score: 0 (indicating the patient is unable to perform the activity) Maximum score: 10 (indicating the patient can perform the activity at their prior level with no difficulty) Interpretation: Higher scores indicate better functional status. The average score across all selected activities will be used for analysis.

    Four Weeks

  • SLR (Straight Leg Raise)

    A clinical test used to assess sciatic nerve irritation or lumbar radiculopathy by raising the extended leg while the patient lies supine.

    Four Weeks

Study Arms (3)

Combined Neural Mobilization with Manual myofascial Release

EXPERIMENTAL

Combined neural mobilization of Sciatic nerve and manual myofascial release of piriformis and back muscles will be given to this group.

Other: Combined Neural Mobilization with Manual myofascial Release

Neural Mobilization

ACTIVE COMPARATOR

Only neural mobilization of Sciatic nerve will be given to this group.

Other: Neural Mobilization

Manual Myofascial Release

ACTIVE COMPARATOR

Only manual myofascial release of piriformis and back muscles will be given to this group.

Other: Manual Myofascial Release

Interventions

Combined neural mobilization with manual myofascial release will be provided to each subject.

Also known as: Neural Mobilization, Manual Myofascial Release
Combined Neural Mobilization with Manual myofascial Release

neural mobilization will be provided to each subject.

Also known as: Combined Neural Mobilization with Manual myofascial Release, Manual Myofascial Release
Neural Mobilization

Manual myofascial release will be provided to each subject.

Also known as: Combined Neural Mobilization with Manual myofascial Release, Neural Mobilization
Manual Myofascial Release

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Clinically diagnosed unilateral sciatic pain for \>3 months.
  • Positive Straight Leg Raise (SLR).

You may not qualify if:

  • \- Participants fall in this category would be excluded of the study.
  • Recent spinal surgery or trauma.
  • Neurological deficits or systemic conditions affecting the nervous system.
  • Any other red flags

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Riphah International University, Malakand

Chakdara, KPK, 18800, Pakistan

Location

MeSH Terms

Conditions

Sciatica

Condition Hierarchy (Ancestors)

Sciatic NeuropathyMononeuropathiesPeripheral Nervous System DiseasesNeuromuscular DiseasesNervous System DiseasesNeuralgiaPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Amnah Anum, MSPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 7, 2025

First Posted

April 27, 2025

Study Start

April 15, 2025

Primary Completion

October 3, 2025

Study Completion

December 31, 2025

Last Updated

April 8, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations