This study would be implemented on the healthy subjects.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Mission experience in the organization for at least 10 years No smoking No previous cardiovascular, blood, liver, kidney or respiratory diseases At least 40 years of age No use of androgenic and ergogenic supplements for at least 3 months before the tes
Exclusion criteria
Exclusion criteria: Outfit the prerequisitive age range of 40 to 50 years old Adding drug treatments that interfere with the hormonal profile or performance of volunteers Subjects' absence Irregular participation in training programs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plasma levels of Osteoprotegerin. Timepoint: Before and 48 hours subsequent to the training session/supplementation. Method of measurement: Elisa technique.;Plasma levels of receptor activator of nuclear factor kappa-?. Timepoint: Before and 48 hours subsequent to the training session/supplementation. Method of measurement: Elisa technique.;Plasma levels of receptor activator of nuclear factor kappa-? ligand. Timepoint: Before and 48 hours subsequent to the training session/supplementation. Method of measurement: Elisa technique.;Bone mass density. Timepoint: Before and 48 hours subsequent to the training session/supplementation. Method of measurement: Dual-energy X-ray absorptiometry (DEXA). | — |
Countries
Iran (Islamic Republic of)
Contacts
Artesh University of Medical Sciences