Low back pain
Conditions
Interventions
A total of 105 individuals will be selected and divided into 4 groups of Aussie (CA): CA1 (n = 25), CA2 (n = 25), CA3 (n = 25), CA4= 25) and placebo group.
All groups will be submitted to 10 sessions
Device
E02.331
Sponsors
Universidade Federal do Paraná
Universidade Federal do Paraná
Eligibility
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: localized lumbar pain; pain analogic visual scale (AVS) more than 3 ; with more than 6 weeks; characterized chronic lumbar pain; lumbar pain with mechanic ethiology.
Exclusion criteria
Exclusion criteria: Participants who have had surgery in the lower back; not presenting back pain radiated to the buttocks and lower limbs, alteration of thermal and / or sensory sensitivity, pregnant women, kidney problems; patients with pacemakers; skin lesions; use of medication for lumbar pain relief 48 hours before the application of the technique. do not have clinical diagnosis of low back pain and when the etiology of back pain is unknown.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Presentation of the method to verify ustilization for lumbar pain decrease by increase of pain threshold evaluated in Kgf by pression algometry after Aussie current aplication. | — |
Secondary
| Measure | Time frame |
|---|---|
| The first frame will contain the first expected outcome. This will be identified as Expected outcome 1: abolition ou decrease of low back pain verified in pain analogic visual scale for at least one point in scale;Expected outcome 2:Decreased subjective perception of pain by decreasing the number of words chosen in the questionnaire of Mcgill after Aussie current aplication. ;Expected outcome 3:Decreased subjective perception of pain by decreasing the percentage assessed in the questionnaire Oswestry after Aussie current aplication. ;Expected outcome 4:Decrease in disability by reducing the number of phrases in the chosen Questionnaire Roland Morris Disability after Aussie current aplication. ;Expected outcome 5:To verify the influence of the biopsychosocial factors to the treatment with the current Aussie after Aussie current aplication with start back questionnaire. ;Expected outcome 6: Improvement of functional capacity and risk of falls through the sit-up test;Expected outcome 7: Evaluate the participant's self-perception regarding treatment before and after CA;Expected outcome 8: Assess depression and anxiety before and after CA;Expected outcome 9: Assess participant satisfaction with treatment before and after CA;Expected outcome 10: Evaluate musculoskeletal condition before and after CA | — |
Countries
Brazil
Contacts
Public ContactAna Carolina de Macedo
Universidade Federal do Paraná
Outcome results
None listed