BDNF
Conditions
Interventions
The study design is characterized by a randomized crossover clinical trial with two arms. According to the sample size calculation, 20 males aged 18 to 30 years will be required, 10 of whom are untrai
Sponsors
Universidade Federal de Ouro Preto
Pontifícia Universidade Católica de Minas Gerais
Eligibility
Sex/Gender
Male
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: To be between 18 and 30 years old; to be male; not to be strength trained; to be strength trained; to have no positive responses on the fitness questionnaire for physical activity; to have no cardiovascular disease risk factors classified as moderate or high risk; to have no recent injuries, pathologies, or health conditions that could be aggravated by the procedures; to not be using substances that could interfere with the experimental procedures; to maintain similar food consumption on the days of the tests and the performance of the training protocols and blood collections
Exclusion criteria
Exclusion criteria: Failure to attend scheduled research phases; failure to follow recommendations the day before the one-repetition maximum test and training protocols; inability to complete the research protocol; impediment to proper blood collection; any health incident during the research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The low-intensity strength training protocol is expected to increase plasma Irisin and BDNF concentrations more than the high-intensity protocol. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected that the group of non-strength-trained individuals will increase plasma Irisin and BDNF concentrations more than the strength-trained group. | — |
Countries
Brazil
Contacts
Public ContactRony Las Casas
Universidade Federal de Ouro Preto
Outcome results
None listed