over weaight woman.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The criteria for entering the study include the absence of any ischemic heart disease, kidney, , non-use of lipid lowering drugs the inability of people to participate in a specific weight loss program the inability of people to participate in a specific physical program woman with over weight 35-45 year old
Exclusion criteria
Exclusion criteria: Interrupting or not participating in exercises Do not take vitamin D supplements Participant withdrawal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dpp4. Timepoint: At the beginning and end of the study. Method of measurement: DPP4 using the biometric group of Australian group kit by ELISA method.;Rbp4. Timepoint: At the beginning and end of the study. Method of measurement: Rbp4 using the biometric group of Australian group kit by ELISA method. | — |
Secondary
| Measure | Time frame |
|---|---|
| Serum insulin concentration. Timepoint: Before the intervention and after eight weeks of study. Method of measurement: , Serum insulin concentration by ELISA method and use of special kit, Monobind Inc., USA) (75 µg / ml micro-unit per ml, intra-group variation coefficient of 6.3%),.;Serum glucose concentration. Timepoint: Before the intervention and after eight weeks of study. Method of measurement: , Serum glucose concentration was measured by enzymatic calorimetric method (sensitivity of 5 ml / dl and internal variation coefficient of 2.5%).;Insulin resistance. Timepoint: Before the intervention and after eight weeks of study. Method of measurement: Insulin resistance was used to evaluate the HOMA-IR homeostasis model by measuring insulin and fasting glucose according to the following formula.Serum glucose level in fasting state (MI / L). Serum insulin level in fasting state (MIU / L). Insulin resistance.5/22. | — |
Countries
Iran (Islamic Republic of)
Contacts
Islamic Azad University