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Recruiting NCT07334756

Non-Thrust Lumbar and Sacral Mobilizations in Mechanical Low Back Pain

No phase Interventional Mechanical Low Back Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Lumbar Mobilizations, Lumbar and sacral mobilizations.
Who it may be relevant to
Registry conditions: Mechanical Low Back Pain. Basic parameters: 18 years — 45 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study is a randomized controlled trial and the purpose of this study is to determined the effects of sacral mobilizations along with the lumbar mobilizations in mechanical low back pain on components such as pain , lumbar range of motion, lumbar proprioception and functional disability.

Detailed description

This study is based on the concept the sacral hypomobility can cause low back pain. Sacral and lumbar mobilizations both improve low back pain.

Interventions

  • Procedure Lumbar Mobilizations
    Lumbar mobilization protocol: Grade II or III lumbar stretch mobilization on lumbar hypomobile segments. Therapeutic exercise protocol: Therapeutic exercise protocol include warmup, strengthening and cool down phase.
  • Procedure Lumbar and sacral mobilizations
    Lumbar mobilization protocol: Grade II or III lumbar stretch mobilization on lumbar hypomobile segments. Sacral Mobilization protocol: Grade II or III sacral mobilization as sacral stretch mobilizations. Therapeutic exercise protocol: Therapeutic exercise protocol include warmup, strengthening and cool down phase.

Primary outcome measures

  • Pain intensity [Time frame: 2 weeks]
  • Lumbar Range of Motion [Time frame: 2 weeks]
  • Functional Disability [Time frame: 2 weeks]
  • Lumbar Proprioception [Time frame: 2 weeks]

Eligibility criteria

  • Inclusion Criteria Adults 18 to 45 years Both genders Low back (from T12 to buttock line) pain for more than 3 months The CMLBP is the chief complaint without leg pain.
  • Exclusion Criteria Acute flare Low Back Pain Thoracic pain Trauma to the spine causing fracture and disruption of the ligaments Leg symptoms when walk, eased in flexion (Signs of stenosis) Paresthesia/numbness Structural deformity (scoliosis, spondylosis, spondylolisthesis) Curve reversal Pregnancy Post-surgery (within 6 months of abdominal or spinal/lower limb surgery) Degenerative and inflammatory spinal diseases Malignancy Centralization and peripheralization

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Foundation University Islamabad — Islamabad

Identifiers

NCT: NCT07334756 · FUI/CTR/2025/27

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗