healthy people.
Conditions
Interventions
Intervention 1: Control group: During this 6-week period, no activity will be involved, nor will any use be made. Intervention 2: First Intervention group: High-Intensity interval training (40 m round
Sponsors
The University of Sistan and Baluchestan
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Completion of consent form for cooperation in research work. Non-public physical education physical education male students that have 1 to select units. Subjects do not have regular physical activity during the last 6 months. At least 6 months before the start of the study, they did not use omega-3 supplements, antioxidants or certain medications. Lack of specific disease and having physical health of subjects. Non-use of cigarettes and tobacco.
Exclusion criteria
Exclusion criteria: Physical Education Students or Students who Have Elected Physical Education 2. Failure to complete the consent form for cooperation in the research project. Subjects with respiratory, cardiac or other diseases. Subjects use a specific drug or supplement 6 months before or at the present time. Subjects have regular activities such as walking, bodybuilding, soccer and ... in the last 6 months or now. Smoking or tobacco use.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum levels of Brain-derived neurotrophic factor (BDNF). Timepoint: Measuring serum BDNF levels at the beginning of the study 24 hours before the start of the The first session of the training and at the end (6 weeks) 48 hours after the last training session. Method of measurement: Blood serum sampling-Laboratory kit for serum human BDNF. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hematology Indicators. Timepoint: At the beginning of the study, 24 hours before the start of the protocol and at the end of the protocol (6 weeks), 48 hours after the last session of the protocol. Method of measurement: American Sysemox Electron Microscope.;Weight. Timepoint: At the beginning of the study, 24 hours before the start of the protocol and at the end of the protocol (6 weeks), 48 hours after the last session of the protocol. Method of measurement: German Seca Digital Scale.;Blood pressure. Timepoint: At the beginning of the study, 24 hours before the start of the protocol and at the end of the protocol (6 weeks), 48 hours after the last session of the protocol. Method of measurement: Pressure gauge Japanese ALPK2.;Body fat percentage. Timepoint: At the beginning of the study, 24 hours before the start of the protocol and at the end of the protocol (6 weeks), 48 hours after the last session of the protocol. Method of measurement: Japan's Caliph Yagamy.;Maximum Oxygen Consumption. Timepoint: At the beginning of the study, 24 hours before the start of the protocol and at the end of the protocol (6 weeks), 48 hours after the last session of the protocol. Method of measurement: Test a mile running in the field.;Body mass index. Timepoint: Measuring serum BDNF levels at the beginning of the study, 24 hours before the start of the protocol and at the end of the protocol (6 weeks), 48 hours after the last session of the protocol. Method of measurement: Digital scales and gauges German Seca Model.;Waist to hip. Timepoint: ???At the beginning of the study, 24 hours before the start of the protocol and at the end of the protocol (6 weeks), 48 hours after the last session of the protocol. Method of measurement: Strip meter.;Lipid Profiles. Timepoint: ???At the beginning of the study, 24 hours before the start of the protocol and at the end of the protocol (6 weeks), 48 hours after the last session of the protocol. Method of measurement: Blood serum sampling, Speci | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSajjad karimi pour
The University of Sistan and Baluchestan
Outcome results
None listed