The effect of high intensity training with taking curcumin supplement on oxidative defense and lipid degradation

The effect of 6 weeks of high intensity training on supplementation of nano-curcumin on anti-oxidative and lipid peroxidation indices in overweight girls

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180927041150N1

Enrollment

Registered

2019-08-29

Start date

2019-09-05

Completion date

Unknown

Last updated

2019-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

obosity and overweight.

Interventions

Intervention 1: The training group will perform high intensity interval training with 85% to 95% maximum heart rate for 6 weeks (3 sessions per week). Intervention 2: The training-supplement group wil

Eligibility

Sex/Gender

Female

Age

18 Years to 28 Years

Inclusion criteria

Inclusion criteria: Having a BMI between 25 and 30 Kilograms per square meter Having physical and mental health Having low activity level Having age between 18 and 28 years

Exclusion criteria

Exclusion criteria: taking medicine or supplement , Alcohol and smoking Being infected various diseases Such as diabetes, thyroid, hypertension, respiratory heart disease

Design outcomes

Primary

Measure	Time frame
Malondialdehyde was considered as a lipid degradation mark. Timepoint: Measurement of malondialdehyde levels prior to the start of a 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory and spectrophotometric method.;Superoxide dismutase was considered as an antioxidant index. Timepoint: Measurement of superoxide dismutase levels prior to the beginning of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.;Glutathione peroxidase was considered as an anxiolytic agent. Timepoint: Measurement of glutathione peroxidase levels before the beginning of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.;Catalase was considered as an anxiolytic agent. Timepoint: Measurement of catalase levels before the beginning of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.;Glutathione was considered as an anxiolytic agent. Timepoint: Measurement of glutathione levels before the start of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.;Total antioxidant capacity was considered as anxiolytic index. Timepoint: Measurement of total antioxidant capacity levels before the start of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.	—

Measure

Time frame

Malondialdehyde was considered as a lipid degradation mark. Timepoint: Measurement of malondialdehyde levels prior to the start of a 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory and spectrophotometric method.;Superoxide dismutase was considered as an antioxidant index. Timepoint: Measurement of superoxide dismutase levels prior to the beginning of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.;Glutathione peroxidase was considered as an anxiolytic agent. Timepoint: Measurement of glutathione peroxidase levels before the beginning of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.;Catalase was considered as an anxiolytic agent. Timepoint: Measurement of catalase levels before the beginning of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.;Glutathione was considered as an anxiolytic agent. Timepoint: Measurement of glutathione levels before the start of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.;Total antioxidant capacity was considered as anxiolytic index. Timepoint: Measurement of total antioxidant capacity levels before the start of the 6-week training period and 48 hours after the end of the training period. Method of measurement: Laboratory.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomaye Fakhri

Shahid Chamran university of Ahvaz

fakhri.somaye@gmail.com+98 71 3750 0104

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026