Effect of Thoracic Mobilization on Lumbar Radiculopathy

Cairo University34 enrolled

Overview

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.

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Lumbosacral Radiculopathy

Interventions

thoracic mobilizationOTHER

Thoracic mobilization will be performed for the thoracic spine mobilization group, thoracic mobilization therapy will be performed for five minutes.

Eligibility

Sex: ALLMin age: 30 YearsMax age: 45 Years

Medical Language ↔ Plain English

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 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.

Locations (1)

Faculty of Physical Therapy Cairo University

Cairo, Egypt

RECRUITING

Outcomes

Primary Outcomes

functional disability

we will use Oswestry Disability Index (ODI)

Time frame: baseline

pain level

we will use Visual analogue scale (VAS)

Time frame: baseline

lumbar proprioception

we will use The Biodex System 3 pro isokinetic dynamometer

Time frame: baseline

Central Contacts

aya abd elmohsen, Bachelor's

CONTACT

01122935258 ayamohsen214@gmail.com

Data from ClinicalTrials.gov

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