Effect of Thoracic Spine Mobilization on Pain, Functional Disability and Proprioception in Patients With Lumbosacral Radiculopathy.
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Cairo University
- Enrollment
- 34
- Locations
- 1
- Primary Endpoint
- pain level
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- 30 Years to 45 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients with unilateral chronic lumbosacral radiculopathy at L4- L5 or / and L5-S1 levels confirmed by MRI.
- •The age of patients will be ranged from 30 to 45 years.
- •Duration of pain will be more than 12 weeks.
- •Patients with a positive straight leg raising (SLR) test.
- •Patients with sufficient cognitive abilities that enables them to understand and follow instructions .
- •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.
- •Patients with body mass index< 30kg/m2
Exclusion Criteria
- •Cauda equina syndrome.
- •Ankylosing spondylitis, thoracic deformities (pectus carinatum, excavatum), spina bifida, fractures, postoperative spinal conditions, diabetes, inflammatory processes.
- •Previous inner ear infection or vestibular disorder with unresolved balance disturbance, history of head trauma with residual neurological deficits.
- •Spinal tumor.
- •Previous lumbar surgery.
- •Sever musculoskeletal disease.
- •Peripheral mononeuropathies or polyneuropathy.
Outcomes
Primary Outcomes
pain level
Time Frame: baseline
we will use Visual analogue scale (VAS)
lumbar proprioception
Time Frame: baseline
we will use The Biodex System 3 pro isokinetic dynamometer
functional disability
Time Frame: baseline
we will use Oswestry Disability Index (ODI)
Secondary Outcomes
No secondary outcomes reported
Investigators
aya abd elmohsen salah eldeen
aya abd elmohsen salah eldeen
Cairo University