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Effect of Thoracic Mobilization on Lumbar Radiculopathy

Not Applicable
Recruiting
Conditions
Lumbosacral Radiculopathy
Interventions
Other: thoracic mobilization
Registration Number
NCT06167044
Lead Sponsor
Cairo University
Brief Summary

The purpose of the study will be to:

* To investigate the effect of thoracic mobilization on back and leg pain in patients with lumbosacral radiculopathy.

* To investigate the effect of thoracic mobilization on functional disability in patients with lumbosacral radiculopathy.

* To investigate the effect of thoracic mobilization on proprioception in patients with lumbosacral radiculopathy.

Detailed Description

To investigate the effect of thoracic mobilization on back and leg pain, functional disability and proprioception in patients with lumbosacral radiculopathy.

1-Thirty four patients of both sexes with unilateral chronic lumbar radiculopathy at L4-L5 or/ and L5-S1 levels will participate in this study. The patients will be diagnosed as having lumbar radiculopathy based on careful clinical examination by neurologist . The diagnosis will be confirmed by CT scan or MRI.

Patients will be recruited from the outpatient clinic of Faculty of Physical Therapy, Cairo University and private clinics. Patients in this study will be randomly divided into two groups.

* Group (I) which will include 17 patients who will receive manual mobilization exercises in addition to selected physical therapy .

* Group (II) which will include 17 patients who will receive selected physical therapy.

The treatment will conducted 3 sessions per week for 6 weeks.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
34
Inclusion Criteria
  1. Patients with unilateral chronic lumbosacral radiculopathy at L4- L5 or / and L5-S1 levels confirmed by MRI.
  2. The age of patients will be ranged from 30 to 45 years.
  3. Duration of pain will be more than 12 weeks.
  4. Patients with a positive straight leg raising (SLR) test.
  5. Patients with sufficient cognitive abilities that enables them to understand and follow instructions .
  6. Patients had to report an average pain level of more than five on the Visual Analogue Scale (VAS) and a lumbar spine range of motion (ROM) of at least 50% of the accepted normal range.
  7. Patients with body mass index< 30kg/m2
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Exclusion Criteria
  1. Cauda equina syndrome.
  2. Ankylosing spondylitis, thoracic deformities (pectus carinatum, excavatum), spina bifida, fractures, postoperative spinal conditions, diabetes, inflammatory processes.
  3. Previous inner ear infection or vestibular disorder with unresolved balance disturbance, history of head trauma with residual neurological deficits.
  4. Spinal tumor.
  5. Previous lumbar surgery.
  6. Sever musculoskeletal disease.
  7. Peripheral mononeuropathies or polyneuropathy.
  8. Obesity .
  9. Pregnancy.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
thoracic mobilization groupthoracic mobilizationwhich will include 17 patients who will receive thoracic manual mobilization exercises in addition to selected physical therapy .The treatment will conducted for 45 minutes, 3 sessions per week for 6 weeks.
Primary Outcome Measures
NameTimeMethod
pain levelbaseline

we will use Visual analogue scale (VAS)

lumbar proprioceptionbaseline

we will use The Biodex System 3 pro isokinetic dynamometer

functional disabilitybaseline

we will use Oswestry Disability Index (ODI)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Faculty of Physical Therapy Cairo University

🇪🇬

Cairo, Egypt

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