Type 2 diabetes mellitus. Diabetes mellitus due to underlying condition
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Suffering from type 2 diabetes mellitus for more than 6 months. taking oral anti-diabetic medications suffering from mild-to-moderate depression
Exclusion criteria
Exclusion criteria: injection of insulin or liraglutide taking medicinal herbs or herbal medicine, antibiotics, antioxidant supplements (multivitamins & minerals, vitamin E, vitamin C, Zinc), suffering from severe depression, having chronic heart -vascular diseases, severe depression, chronic liver chronic liver and kidney disease, uncontrolled thyroid and any other diabetes complications leads to inflammatory and oxidative conditions, other types of diabetes taking psychiatry medications. Pregnancy and lactation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Depression. Timepoint: Baseline, after 8 weeks of the intervention (At the end of the intervention). Method of measurement: Montgomery-Asberg Depression Rating Scale (MADRS).;Fat mass. Timepoint: Baseline, after 4 weeks of intervention and At the end of the intervention. Method of measurement: Bio-Electrical Impedance Analysis.;Fat free mass. Timepoint: Baseline, after 4 weeks of intervention and At the end of the intervention. Method of measurement: Bio-Electrical Impedance Analysis.;HbA1c. Timepoint: Baseline, At the end of the intervention. Method of measurement: Chromatography. | — |
Secondary
| Measure | Time frame |
|---|---|
| Advanced glycation end products. Timepoint: Baseline, At the end of the intervention. Method of measurement: ELISA kit.;FBS. Timepoint: Baseline, At the end of the intervention. Method of measurement: Autoanalyzer.;Total cholesterol. Timepoint: Baseline, At the end of the intervention. Method of measurement: Autoanalyzer.;Low-density lipoprotein. Timepoint: Baseline, At the end of the intervention. Method of measurement: Autoanalyzer.;High-density lipoprotein. Timepoint: Baseline, At the end of the intervention. Method of measurement: Autoanalyzer.;High-sensitivity C-reactive protein. Timepoint: Baseline, At the end of the intervention. Method of measurement: ELISA kit. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tehran University of Medical Sciences