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Investigation of Immediate, Short and Long Term Effects of Mulligan Mobilization With Movement Techniques in Nonspesific Chronic Low Back Pain

Investigation of Immediate, Short and Long Term Effects of Mulligan Mobilization With Movement Techniques in Nonspesific Chronic Low Back Pain: a Randomized Placebo-controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04802850
Enrollment
36
Registered
2021-03-17
Start date
2013-01-01
Completion date
2015-04-01
Last updated
2021-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Low Back Pain

Brief summary

Introduction: Although the effectiveness of many mobilization methods in chronic low back pain (CLBP) was shown, these effects were not monitored in the long term. The aim of this study was to identify the immediate, short and long-term effects of mulligan mobilization with movement (MWM) in terms of pain, range of motion (ROM), flexibility, endurance, functionality and disabilities in patients with CLBP. Methods: The study was designed in randomized-placebo controlled with 36 people randomly distributed into 2 groups. Sustained natural apophyseal glide (SNAG) was applied to the lumbar region, straight leg raise (SLR) with traction to the hip, and internal rotational mobilization techniques and home exercise program were applied in Group 1 (n=19); and the same techniques were applied as sham mobilization in Group 2 (n=17). The evaluations were made as post-intervention for immediate effect, and were also made at the 5th week, 3rd month, and 6th months for short and long-term effect. Evaluation was also made for pain in 12th month.

Interventions

Sponsors

Suleyman Demirel University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Having 3 months' continuous or intermittent LBP symptoms, without leg pain above the knee * Pain at VAS \> 3/10, * Back pain increased by active lumbar flexion movement

Exclusion criteria

* Confirmed nerve root compression * Neurological symptoms * Lumbar spine stenosis * Back surgery history * Chronic pain syndrome * LBP from fracture * Infection * Visceral disease * Pregnancy * Major clinical depression * Cauda equina syndrome * Significant osteoporosis.

Design outcomes

Primary

MeasureTime frameDescription
Flexibilityimmediate(post intervention)-5 weeeks(after 5 week treatment)-3 months(after 3 months)-6 months(after 6 months)Change of lumbar flexibility with sit and reach objective test( cm)
Enduranceimmediate(post intervention)-5 weeeks(after 5 week treatment)-3 months(after 3 months)-6 months(after 6 months)Change of endurance of lumbar extensors with Sorensen endurance test(sn)
Functionality with patient specific function scaleimmediate(post intervention)-5 weeeks(after 5 week treatment)-3 months(after 3 months)-6 months(after 6 months)Change of function
Disabilities with Oswestry disability index(scale)immediate(post intervention)-5 weeeks(after 5 week treatment)-3 months(after 3 months)-6 months(after 6 months)Change of disabilities

Secondary

MeasureTime frameDescription
range of motion with goniometerimmediate(post intervention)-5 weeeks(after 5 week treatment)-3 months(after 3 months)-6 months(after 6 months)-12 monthschange of range of motion

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026