The subject is not the disease.
Conditions
Interventions
Intervention 1: Intervention group1:They do moderate intensity combined training (plyometric and resistance) is performed for 1 hour, 3 days a week for 8 weeks. Intervention 2: Intervention group 2: P
Sponsors
Artesh University of Medical Sciences
Eligibility
Sex/Gender
Male
Age
30 Years to 45 Years
Inclusion criteria
Inclusion criteria: Male military personnel working in the city of Tabriz Age between 30 to 45 years
Exclusion criteria
Exclusion criteria: Not doing regular exercise No smoking No history of cardiovascular disease No blood diseases No liver disease No respiratory diseases Do not take anti inflammatory drugs and bronchodilators (beta-receptor agonists) such as salbutamol and nonsteroidal analgesics.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pulmonary capacities. Timepoint: Before training and 48 hours after the last training session. Method of measurement: Spirometer.;Clara 16 protein in serum. Timepoint: Before training and 48 hours after the last training sessio. Method of measurement: Eliza.;Surfactant D protein in serum. Timepoint: Before initiation of training and 48 hours after the last training session. Method of measurement: Eliza.;Cardiovascular fitness. Timepoint: Before initiation of training and 48 hours after the last training session. Method of measurement: Measurement the time required to run 3000 meters. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contact?Simin Riahy
Artesh University of Medical Sciences
Outcome results
None listed