Overweight and obesity. Overweight and obesity
Conditions
Interventions
Intervention 1: Intervention Group 1: Two exercise sessions per week + caloric restriction (a daily deficit of 360 kcal). In addition, each exercise session will involve an energy expenditure of appro
Sponsors
Tehran University
Eligibility
Sex/Gender
Female
Age
19 Years to 50 Years
Inclusion criteria
Inclusion criteria: Body Mass Index (BMI) between 27 and 35 No use of specific medications No underlying diseases such as diabetes
Exclusion criteria
Exclusion criteria: Physical problems that prevent engagement in physical activity Under medical treatment or following a specific diet
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endocan. Timepoint: Endocan levels are measured through blood tests one week before the intervention begins and 60 days after the intervention period ends. Method of measurement: Endocan levels are measured through blood tests using ELISA kits.;Interleukin-6. Timepoint: Interleukin-6 levels are measured through blood tests one week before the intervention begins and 60 days after the intervention period ends. Method of measurement: Interleukin-6 levels are measured through blood tests using ELISA kits. | — |
Secondary
| Measure | Time frame |
|---|---|
| Weight. Timepoint: Weight measurement is at the beginning of the study (before the start of the intervention) and 60 days after the start of the intervention. Method of measurement: A scale is used to measure weight.;Body Fat Percentage. Timepoint: Body Fat Percentage is at the beginning of the study (before the start of the intervention) and 60 days after the start of the intervention. Method of measurement: Body fat percentage will be measured using a body composition analyzer (InBody 270).;Muscle mass. Timepoint: Muscle mass is at the beginning of the study (before the start of the intervention) and 60 days after the start of the intervention. Method of measurement: Muscles mass will be measured using a body composition analyzer (InBody 270).;Visceral Fat Levels. Timepoint: Visceral Fat Levels is at the beginning of the study (before the start of the intervention) and 60 days after the start of the intervention. Method of measurement: Visceral Fat Levels will be measured using a body composition analyzer (InBody 270). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactKatayoun Zamani
Tehran University
Outcome results
None listed