Effectiveness of Combined Neural Mobilization With Manual Myofascial Release for Sciatic Pain Relief
1 other identifier
interventional
48
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2025
Shorter than P25 for not_applicable
1 active site
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
CompletedStudy Start
First participant enrolled
April 15, 2025
CompletedFirst Posted
Study publicly available on registry
April 27, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 3, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedApril 8, 2026
April 1, 2026
6 months
April 7, 2025
April 2, 2026
Conditions
Keywords
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
EXPERIMENTALCombined neural mobilization of Sciatic nerve and manual myofascial release of piriformis and back muscles will be given to this group.
Neural Mobilization
ACTIVE COMPARATOROnly neural mobilization of Sciatic nerve will be given to this group.
Manual Myofascial Release
ACTIVE COMPARATOROnly manual myofascial release of piriformis and back muscles will be given to this group.
Interventions
Combined neural mobilization with manual myofascial release will be provided to each subject.
neural mobilization will be provided to each subject.
Manual myofascial release will be provided to each subject.
Eligibility Criteria
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
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Amnah Anum, MSPT
Riphah International University
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