Effect of high and low volume of specific training for the trunk in chronic low back pai
- Conditions
- low back painC23.888.592.612.107
- Registration Number
- RBR-5328h8g
- Lead Sponsor
- niversidade Federal de Sergipe
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- Not specified
Women with a clinical diagnosis of chronic nonspecific low back pain; age between 18 and 59 years; complaint of low back pain for more than 3 months; pain level greater than 3 on the 11-point numerical pain scale; body mass index (BMI) <30 kg/m2; not having undergone spinal surgery; not practicing physical exercise regularly; not having physical therapy or other pain treatment; not taking analgesic, anti-inflammatory, opioid or immunosuppressive medication
Missing one of the assessments; missing more than 10% of the intervention; have any motor, psychiatric or cognitive impairment; have hearing, visual or communication disorders
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the physiological mechanisms involved in core stabilization training, analyzed by the method of evaluating trunk muscle function and plasma levels of cytokines and beta-endorphin and presentation of parameters of strength, endurance, trunk stability and circulating levels of beta endorphin and cytokines in blood plasma, observed to analyze which training volume is most effective to activate endogenous pain modulation circuits in women with chronic nonspecific low back pain
- Secondary Outcome Measures
Name Time Method To evaluate the function of the trunk muscles, through the method of evaluating the strength, endurance and stability of the trunk and presentation of the percentage of strength, resistance and stability of this musculature, observed to analyze the most effective training volume to promote improvement in function of the trunk;To evaluate the profile of cytokines and plasma beta-endorphin, through the method of blood collection and presentation of the percentage of interleukin (IL)-6, tumor necrosis factor (TNF)-a, interleukin (IL)-10 and plasma levels of ß-endorphins, observed to analyze which training volume is most effective to promote pain reduction