healthy people.
Conditions
Interventions
Intervention 1: Intervention group: Receive Compact Food ration with pragmatic and beneficial compounds for 10 days. Intervention 2: Control group: Receive Compact Food ration without pragmatic and b
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Male
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Military personnel are maneuvering operations Age range 18-50 years Do not use antioxidant and herbal supplements at least 1 month before starting the study Willingness to cooperate and sign a conscientious consent form after full knowledge of the goals and method of the study
Exclusion criteria
Exclusion criteria: Special Diet for at least 6 months History of any allergies and allergies to certain compounds smoking Use of any antioxidant and anti-inflammatory nutritional supplement during the study Unwillingness to participate in the study or continue cooperation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total antioxidant capacity. Timepoint: At baseline and after 10 day of intervention. Method of measurement: blood sample.;Malondialdehyde. Timepoint: At baseline and after 10 day of intervention. Method of measurement: Spectrophotometry.;High-sensitivity C-reactive protein. Timepoint: At baseline and after 10 day of intervention. Method of measurement: Immunoturbidimetry. | — |
Secondary
| Measure | Time frame |
|---|---|
| Maximum rate of oxygen consumption (vo2max). Timepoint: At baseline and after 10 day of intervention. Method of measurement: step test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Gholamreza Askari
Esfahan University of Medical Sciences
Outcome results
None listed