cardiovascular risk factor. Atherosclerosis
Conditions
Interventions
Intervention 1: Intervention group: Subjects in aerobic training group underwent aerobic training for eight weeks, 3 sessions per week for 60 min. Subjects of this group doing aerobic training with in
Sponsors
Research Council of Zahedan Branch, Islamic Azad University
Eligibility
Sex/Gender
Male
Age
20 Years to 25 Years
Inclusion criteria
Inclusion criteria: Student aged 20-25 years Healthy without chronic diseases Do not do regular exercises in the last two years
Exclusion criteria
Exclusion criteria: Less than 20 years old or older than 25 years Having any history of chronic diseases Doing regular exercise during the last two years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visfatin. Timepoint: Eight weeks. Method of measurement: By collecting venous blood before and at the end of study and measuring serum levels of related factors using Enzyme-linked immunosorbent assay (ELISA).;Homocysteine. Timepoint: Eight weeks. Method of measurement: By collecting venous blood before and at the end of study and measuring serum levels of related factors using Enzyme-linked immunosorbent assay (ELISA).;C-reactive protein. Timepoint: Eight weeks. Method of measurement: By collecting venous blood and measuring serum levels of related variables before and at the end of the study by immunotherapy meter method.;Weight. Timepoint: Eight weeks. Method of measurement: By the scale.;Body mass index. Timepoint: Eight weeks. Method of measurement: By the body composition analyzer.;LDL-C. Timepoint: Eight weeks. Method of measurement: By collecting venous blood and measuring serum levels of related variables before and at the end of the study by enzymatic method.;HDL-C. Timepoint: Eight weeks. Method of measurement: By collecting venous blood and measuring serum levels of related variables before and at the end of the study by enzymatic method.;TG. Timepoint: Eight weeks. Method of measurement: By collecting venous blood and measuring serum levels of related variables before and at the end of the study by enzymatic method.;TC. Timepoint: Eight weeks. Method of measurement: By collecting venous blood and measuring serum levels of related variables before and at the end of the study by enzymatic method. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactKeyvan Hejazi
Toos Institute of Higher Education
Outcome results
None listed