Young Adult
Conditions
Interventions
The study uses a randomized crossover approach. Thus, 20 subjects will perform a series of evaluations immediately, 1 h and 24 h after ischemic preconditioning and control treatment.
The ischemic prec
Other
Sponsors
Centro de Ciências da Saúde e do Esporte - UDESC
Centro de Ciências da Saúde e do Esporte - UDESC
Eligibility
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Healthy volunteers; both sexes; non smokers; age between 18 and 40 years;
Exclusion criteria
Exclusion criteria: Regular use of any type of medication; smokers; osteo-articular lesion in the last twelve months;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement in pain sensitivity, assessed by pressure pain threshold testing with expected increase of at least 10%. Data collected immediately before and after the intervention.;Improvement in pain sensitivity, assessed by the pressure pain threshold testing with an increase of approximately 27%. Data collected immediately before and after the intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement in pain sensitivity up to 24 h after treatment, evaluated by pressure pain threshold testing with expected increase of at least 10%. Data collected immediately before and 0 h, 1 h and 24 h after the intervention.;Improvement in pain sensitivity up to 24 h after treatment, evaluated by the pressure pain threshold testing with increase of approximately 27%, 22% and 17% at 0 h, 1 h and 24 h after treatment, respectively. Data collected immediately before and 0 h, 1 h and 24 h after the intervention.;Improvement in muscle blood flow up to 24 hours after treatment, evaluated by near infrared spectrophotometry with expected increase greater than 20%. Data collected immediately before and 0 h, 1 h and 24 h after the intervention.;Improvement in muscle blood flow up to 1 h after treatment, evaluated by near infrared spectrophotometry with increase of 13.9% and 44.8% at 0 h and 1 h after treatment, but without significant increase at 24 h. Data collected immediately before and 0 h, 1 h and 24 h after the intervention.;Improvement in mitochondrial function, assessed by near-infrared spectrophotometry with expected increase greater than 20%. Data collected immediately before and 0 h, 1 h and 24 h after the intervention.;No significant change in mitochondrial function assessed by near infrared spectrophotometry. Data collected immediately before and 0 h, 1 h and 24 h after the intervention. | — |
Countries
Brazil
Contacts
Public ContactFabrizio Caputo
Centro de Ciências da Saúde e do Esporte - UDESC
Outcome results
None listed