low back pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: For the study are included patients aged 18 to 65 years; patients with a diagnosis of non-specific low back pain with at least three months of progression of pain; patients who signed the informed consent and informed
Exclusion criteria
Exclusion criteria: Patients pregnant women; patients with specific diagnosis that cause low back pain; orthopedic, rheumatic and neurological problems; nerve root injury; patients with impaired cognition; patients undergoing treatment during the study period; patient who underwent pre-treatment at least 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Outcome: improvement of functional disability and pain related to lumbar spine, where the analysis of pain is verified by visual analogue scale and questionnaire mcgill, while the analysis of functional disability will be verified by the questionnaire roland morris after treatment by stabilizing and lumbar segmental stretching in individuals with nonspecific chronic low back from an expected difference (p <0.05) in the pretreatment tests and follow up 6 months and 1 year | — |
Secondary
| Measure | Time frame |
|---|---|
| Don't have second outcomes | — |
Countries
Brazil
Contacts
Universidade Federal do Amapá