Low Back Pain, Pain
Conditions
Keywords
Exercise Movement Techniques, Low Back Pain, Exercise
Brief summary
Lumbar pain is one of the most common injuries being the cause of morbidity in the individual generating occupational disability with strong personal, social and economic impact. As one of the methods of treatment, Pilates is a method that has good results for the management of this dysfunction. However, it is not known exactly which approach Pilates can bring better results for this population. Therefore, the purpose of this study is to compare the effects of two types of Pilates method interventions on non-specific chronic low back pain. A blinded randomized clinical trial, will be held. 28 patients divided randomly into two groups will be assessed, the Mobilization Pilates (MP) and the Stabilization Pilates (SP). Both groups will be formed by individuals of both sexes and aged 21 to 41 years with chronic low back pain. Both groups will receive 10 sessions of Pilates Methods twice a week, with each session taking an average of 50 minutes, therefore the MP will focus on a lumbo-pelvic mobilization exercises approach and the SP will focus on lumbo-pelvic stabilization exercises approach. At the beginning and end of the 5 weeks the individuals are evaluated to verify the presence of pain and disability with VAS of pain and Oswestry Questionnaire, and also with the Functional Movement Screen. Data will be analyzed statistically.
Interventions
OTHERExercise Movement Techniques based on mobilization
10 sessions will be held twice a week, with each session taking an average of 50 minutes.
OTHERExercise Movement Techniques based on stabilization
10 sessions will be held twice a week, with each session taking an average of 50 minutes.
Sponsors
Federal University of Rio Grande do Sul
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
21 Years to 40 Years
Healthy volunteers
No
Inclusion criteria
* Individuals of both sexes aged between 21 and 40 years; * Self-reported low back pain for at least 3 months; * Disability Oswestry Index greater than 10%.
Exclusion criteria
* Diagnosis of pathognomonic low back pain caused by disc herniation with root involvement, inflammatory disorders, infections, osteoporosis, rheumatoid arthritis, fracture or tumor; * Medical contraindication to the practice of Pilates; * Childbirth or gestation in the last 6 months; * Be performing any type of treatment for low back pain is medicated, physiotherapeutic or alternative during the period of intervention; * Change the level of physical or sports activity during the intervention period; * Participants who miss two sessions in a row or four sessions alternately without retrieving them in the same week will automatically be excluded from the survey; Or do not attend pre and post-test evaluation events.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The change in Oswestry Low Back Disability Questionnaire | At the first session and 5 weeks after the intervention | The Oswestry Disability Index (also known as the Oswestry Low Back Pain Disability Questionnaire) is an extremely important tool that researchers and disability evaluators use to measure a patient's permanent functional disability. The test is considered the 'gold standard' of low back functional outcome tools. The oswestry questionarie will be evaluated in the first session and after 5 weeks of Pilates training. So, the primary outcome is the change in the Oswestry score from baseline to 5 weeks. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The change in Visual Analog Scale for Pain (VAS) | At the first session and 5 weeks after the intervention | Pain intensity will be assessed using visual analog scale (VAS), which consists of a 10-cm horizontal line in which 0 means No pain and 10 means The worst pain I can imagine. This visual analog scale for pain will be evaluated in the first session and after 5 weeks of Pilates training. So, this outcome is the change in VAS score from baseline to 5 weeks. |
| The change in The Functional Movement Screen (FMS) | At the first session and 5 weeks after the intervention | The FMS is a screening for individuals who participate in physical activities by identifying limitations and restrictions in completing 7 movement tasks: deep squat, hurdle step, in-line lunch, shoulder mobility, active straight leg raise, trunk stability push-up, and rotatory stability. Each one of these 7 movement tasks are scored on a 0-3 ordinal scale. The FMS output is a single result given by summing each movement's score. The maximum score is 21. The lower the score, the higher is the patient's risk for injury. FMS will be evaluated before and after intervention. So, this outcome is the change in FMS score from baseline to 5 weeks. |
Countries
Brazil
Outcome results
None listed