athlete.
Conditions
Interventions
Intervention 1: Intervention group: curcumin, 500 mg capsule, once per day, for 8 weeks. Intervention 2: control group: placebo of curcumin containing corn starch, 500 mg capsule, once per day, for 8
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 30 Years
Inclusion criteria
Inclusion criteria: willingness to participate in the study Female athletes of Isfahan Not using antioxidant supplements and anti-inflammatory drugs History of at least 3 years of continuous exercise Age between 20-30
Exclusion criteria
Exclusion criteria: following less than 70% , loss to follow up unwillingness to continue, loss to follow up Afflicated by a special diseases smoking
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| C-reactive protein (CRP). Timepoint: The beginning (before intervention) and the end of the study (60 days after intervention). Method of measurement: blood sample.;Total antioxidant capacity. Timepoint: The beginning (before intervention) and the end of the study (60 days after intervention). Method of measurement: blood sample.;Malondialdehyde. Timepoint: The beginning (before intervention) and the end of the study (60 days after intervention). Method of measurement: blood sample.;Lactate dehydrogenase. Timepoint: The beginning (before intervention) and the end of the study (60 days after intervention). Method of measurement: blood sample. | — |
Secondary
| Measure | Time frame |
|---|---|
| Maximum rate of oxygen consumption (vo2max). Timepoint: The beginning (before intervention) and the end of the study (60 days after intervention). Method of measurement: step test.;Body composition. Timepoint: The beginning (before intervention) and the end of the study (60 days after intervention). Method of measurement: Bioimpedance system. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactmina salehi
Esfahan University of Medical Sciences
Outcome results
None listed