Effect of Mulligan Versus Maitland Mobilization on Lumbar Proprioception in Patients With Chronic Nonspecific Low Back Pain
LBP
1 other identifier
interventional
90
1 country
1
Brief Summary
this study will be conducted to compare between the effect of mulligan mobilization versus Maitland mobilization on pain ,function and lumbar proprioception in patients with chronic nonspecific low pain
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable low-back-pain
Started Apr 2025
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 11, 2025
CompletedStudy Start
First participant enrolled
April 15, 2025
CompletedFirst Posted
Study publicly available on registry
April 23, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 31, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 31, 2026
CompletedFebruary 10, 2026
February 1, 2026
10 months
April 11, 2025
February 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
joint position error (lumbar proprioception)
joint position error will be measured by isokinetic. The lumbar Joint Position Error (JPE) Test is a measurement tool used to clinically assess an individual's lumbarcephalic proprioception ability. proprioception describes one's sense of position of their back in space. The lumbar JPE Test measures the ability of a blindfolded patient to accurately relocate their lumbar to a predetermined neutral point after lumbar joint movement.
up to four weeks
Secondary Outcomes (3)
pain intensity
up to four weeks
Functional disability
up to four weeks
lumbar range of motion
up to four weeks
Study Arms (3)
mulligan group
EXPERIMENTALthirty patients will receive mulligan sustained natural apophyseal glide (SNAG) for each level was 3 sets of 6 repetitions 3 times per week for 1 month plus traditional therapy
Maitland mobilization
EXPERIMENTALthirty patients will receive Maitland 3 times per week for 1 month plus traditional therapy
traditional therapy
ACTIVE COMPARATORthirty patients will receive traditional therapy three times a week for four weeks
Interventions
the patients will receive traditional therapy in the form of passive stretching, strengthening, and lumbar stabilization exercises
SNAG technique was applied from a sitting position on the edge of the table while both feet were on a foot rest. A specialized Mulligan belt was used around the patient's waist and therapist's hips. The mobilizing force was applied parallel to the facet joint plane (cephalic direction) and over the spinous processes of the respective symptomatic spinal levels. The patients were asked to lean forward as much as possible during application of the mobilizing force and then return to the starting position while the therapist maintained his mobilizing force until the end. plus traditional therapy
The subjects were placed in the prone position on a plinth with their hands beside them, and the therapist stood on the subject's side, the ulnar surface of the hand (between pisiform and hamate) was placed over the hypomobile spinous process. The second hand was placed on top of the first to enhance its force. With the therapist's elbows slightly bent and shoulders exactly above the spinous process, an oscillatory movement of the vertebra was executed by applying a posterior-anterior force to the hypomobile or painful spinous process. Grade III mobilization was applied four times, each with 60 s of oscillation and 20 s of rest in between them (2 or 3 oscillations per second) plus traditional therapy
Eligibility Criteria
You may qualify if:
- They had interrupted or continuous LBP symptoms for more than 3 months
- both gender
You may not qualify if:
- specific LBP
- those who were pregnant
- those with neurological problems
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Alshaymaa Shaaban Abdelazeim
Giza, Doki, 11251, 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 : alshaymaa shaaban abd el azeim
Study Record Dates
First Submitted
April 11, 2025
First Posted
April 23, 2025
Study Start
April 15, 2025
Primary Completion
January 31, 2026
Study Completion
January 31, 2026
Last Updated
February 10, 2026
Record last verified: 2026-02