Effect of neurodynamic mobilization and motor control training on pain and mechanosensitivity in patients with lumbosacral disc herniation and sciatica
- Conditions
- sciatica painlumbar disc herniationPhysical Medicine / Rehabilitation - PhysiotherapyMusculoskeletal - Other muscular and skeletal disordersNeurological - Other neurological disorders
- Registration Number
- ACTRN12616000200482
- Lead Sponsor
- Gustavo Plaza
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Patients aged between 18 and 60 years old.
L4-L5-S1 disc herniation with pain in lower limb.
At least 3 months with pain
Positive Straight Leg Raise Test
No additional treatment while study is carrying out
Exclusion Criteria
Disc herniations in other spinal levels
Other spinal pathologies like tumours or spondylolisthesis
Acute pain
Patients treated with other treatments.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of participants with a reduction in mechanosensitivity in lower limbs nerves (preassure pain threshold) measured with an algometer[The weekly assessment occur before and after each weekly session. Algometry will be used 2 months after intervention completion too];Proportion of participants with a reduction in pain measured with Visual Analogic Scale and LANSS Questionnaire[LANSS Questionnaire will be used at the beggining of the trial, at the middle (4 weeks) and at the end of the intervention (8 weeks). It will be used also 2 months post intervention completion.<br>Visual Analogic Scale will be used each weekly session (before and after each session) and it will be used also 2 months post intervention completion]
- Secondary Outcome Measures
Name Time Method Proportion of participants with a reduction in low back pain disability, measured with Rolland Morris questionnaire[At the beggining of the intervention, 4 weeks, at the end of the intervention and 2 months post intervention completion]