Comparison of the effect of combined exercise and consumption of three types of tea on overweight me

Phase 3

Recruiting

Conditions: Overweight and obesity.
E66.9
Obesity, unspecified

Registration Number: IRCT20230131057292N2

Lead Sponsor: niversity of Tehran

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Male

Target Recruitment: 60

Inclusion Criteria

Men aged between 30 and 50 years
Body mass index between 25 and 35 kg/m2
Inactivity (less than 30 minutes of sports activity per week)

Exclusion Criteria

Taking any kind of medicine and food supplement
Performing surgery to reduce obesity
Consumption of alcoholic beverages and cigarettes
Subjects' unwillingness to continue the research protocols
Allergy to tea
Participating in sports activities other than the sports program of the present study

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Serum levels of PGC1a. Timepoint: 48 hours before and after the last training session after 12 hours of fasting. Method of measurement: Using the human ELISA diagnostic kit related to the variable.;Serum levels of FGF21. Timepoint: 48 hours before and after the last training session after 12 hours of fasting. Method of measurement: 48 hours before and after the last training session after 12 hours of fasting.

Secondary Outcome Measures

Name	Time	Method
Weight changes. Timepoint: At the beginning of the study (before the start of the intervention) and 8 weeks after the start of the research. Method of measurement: scale.;Waist to hip ratio. Timepoint: At the beginning of the study (before the start of the intervention) and 8 weeks after the start of the research. Method of measurement: Waist to hip ratio.;Body mass index. Timepoint: At the beginning of the study (before the start of the intervention) and 8 weeks after the start of the research. Method of measurement: Bioelectrical impedance device.;Fat index. Timepoint: At the beginning of the study (before the start of the intervention) and 8 weeks after the start of the research. Method of measurement: Bioelectrical impedance device.