Neurodynamic Moblization Versus Mulligan on Pain and Functional Abilities in Patients With Chronic Discogenic Sciatica
DS
Effect of Neurodynamic Mobilization Versus Mulligan on Pain and Functional Abilities in Patients With Chronic Discogenic Sciatica
1 other identifier
interventional
66
1 country
1
Brief Summary
The purpose of the present study to compare between the effect of neurodynamic moblizaton and Mulligan SNAG's moblization on patients with chronic unilateral discogenic sciatica.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 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
June 25, 2025
CompletedFirst Posted
Study publicly available on registry
July 3, 2025
CompletedStudy Start
First participant enrolled
August 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 10, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 28, 2026
CompletedMarch 5, 2026
March 1, 2026
5 months
June 25, 2025
March 3, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
pressure pain threshold
ALgometer offer real-time visual \& auditory feedback to control \& monitor applied pressure rates to measure pressure pain threshold.
up to four weeks
pain intensity
Sciatica Bothersomeness Index will be used to assess pain intensity. An index based on patients reporting of symptoms which reflects the troubled patient is going through with his sciatica symptoms. Items from the Sciatica Bothersomeness Index (0 = none to 6 = extremely) were used to establish values for paresthesia, weakness and leg pain.
up to four weeks
Secondary Outcomes (2)
Range of motion assessment of straight leg raise
up to four weeks
disability
up to four weeks
Study Arms (3)
neurodynamic mobilization
EXPERIMENTALtwenty two patients will receive neurodynamic mobilization and selected physical therapy program three times a week for four weeks
Mulligan therapy
EXPERIMENTALtwenty two patients will receive mulligan therapy and selected physical therapy program three times a week for four weeks
selected physical therapy program
ACTIVE COMPARATORtwenty two patients will selected physical therapy program three times a week for four weeks
Interventions
the patients will receive neurodynamic mobilization in the form of opening technique which include; static opening and dynamic opening. also, sliding and tensioning technique+ selected physical therapy program
sustained natural apophyseal glide SNAGs are mobilisation techniques and are used as part of the Mulligan Concept+ selected physical therapy program The patient position is stitting on the edage of the plenth non weight bearing position. The therapist will stand behind the patient, the therapist will apply SNAG for 3 repetitions during the initial screening session,the patient will be asked to lean forwared while applying the technique .the therapist apply onle from fove to seven repetitions.patients who experienced no worsening or showed improvement of pain and ROM were considered good indication for the effectivness of treatment .
The program of therapeutic exercises consisted of upper and lower back exercises. Each exercise will repeat from ten to thirty times, three repetitions in three sets with rest one to two minutes between the sets. The repetition of each exercise vary according to the physical ability of each patient. Lower back strengthening exercises: From prone lying position, the patient will asked to raise one lower limb then the other then both lower limbs+ TENS and US
Eligibility Criteria
You may qualify if:
- All the patients diagnosed as lumbar radiculopathy (L5-S1) for at least six months. Diagnosis was confirmed by physical, neurological examination (motor assessment, sensory assessment, reflexes) and radiological assessment (CT or MRI).
- All patients has second grade of disc bulge which will detect from T2 axial view of MRI according to Fardon and Milette
- All patients has unilateral radiculopathy and pain in the distribution of scaitic nerve.
- The age of the patients will range from 35 to 50years . Their body mass index will range between( 22-25)
You may not qualify if:
- Bilateral and multilevel disc prolapse or bilateral radtadiating pain
- acute pain (pain less than three months).
- Presence of active infection in lumbar spine.
- Any other spinal deformities.
- Postoperative cases.
- Cauda equine lesion.
- Neoplasmic.
- Spinal stenosis.
- Mechanical low back pain.
- Failed back syndrome.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Faculty of physical therapy, Cairo University
Cairo, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- opaque sealed envelope
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principle investigator : Asmaa ibrahim Attia
Study Record Dates
First Submitted
June 25, 2025
First Posted
July 3, 2025
Study Start
August 10, 2025
Primary Completion
January 10, 2026
Study Completion
January 28, 2026
Last Updated
March 5, 2026
Record last verified: 2026-03