Hearing Loss, Functional
Conditions
Interventions
This is a three-arm, double-blind, randomized controlled clinical trial, characterized as a phase III pilot study. Experimental group 1: 5 adult individuals (18 to 55 years old) diagnosed with profoun
Sponsors
Associação Educativa Evangélica
Centro de Ciências Biológicas e da Saúde CCBS - Universidade Estadual do Oeste do Paraná
Eligibility
Age
17 Years to 59 Years
Inclusion criteria
Inclusion criteria: Participants of both sexes; aged between 18 and 59 years; with persistent and or recurrent low back pain for at least three months; with clinical characteristics compatible with mechanical low back pain
Exclusion criteria
Exclusion criteria: Participants with low back pain of non mechanical origin including oncological inflammatory or rheumatic causes; pregnant women; individuals with a history of spinal surgery; individuals with neurological diseases; participants undergoing concomitant physiotherapeutic treatment for low back pain; and individuals unable to understand study instructions or the consent process
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate self selected walking speed; verified using the 10 meter walk test; speed in meters per second will be analyzed at pre intervention and post intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate maximum walking speed; verified using the 10 meter walk test; speed in meters per second will be analyzed at pre intervention and post intervention;Evaluate locomotor rehabilitation index; estimated from self selected walking speed and optimal walking speed derived from the Froude number equation; percentage values will be analyzed at pre intervention and post intervention;Evaluate static lumbopelvic stability with emphasis on the transversus abdominis; verified using a pressure biofeedback unit; pressure variation in millimeters of mercury will be analyzed at pre intervention and post intervention;Evaluate static lumbopelvic stability with emphasis on the lumbar multifidus muscles; verified using a pressure biofeedback unit; pressure variation in millimeters of mercury will be analyzed at pre intervention and post intervention;Evaluate dynamic lumbopelvic stability; verified using a pressure biofeedback unit during alternate lower limb abduction; pressure variation in millimeters of mercury will be analyzed at pre intervention and post intervention | — |
Countries
BR
Contacts
Public ContactUniversidade ;Alberito de Goiás;Carvalho
Universidade Evangélica de Goiás- UniEVANGÉLICA;Universidade Estadual do Oeste do Paraná
Outcome results
None listed