Evaluate the performance of three different diets (low calorie, balanced, low calorie - low carb and low calories - low fat) on high-sensitivity c-reactive protein and lipid profile in overweight individuals
Phase 2
- Conditions
- Overweight.Overweight
- Registration Number
- IRCT2013100614914N1
- Lead Sponsor
- Vice chancellor for research, Shiraz University of Midical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Individuals must complete a consent form to participate in the project; a certificate of age from 25 to 60 years; no use of lipid-lowering medications; no history of kidney disease; liver disease; heart disease; thyroid disorders, diabetes; and rheumatologic diseases. Exclusion criteria: those who did not fill out a consent form or were withdrawn from the plan; Changes in diet; changes in daily physical activity; pregnancy; lactation or use of oral contraceptives; Conditions that require patients to lipid-lowering drugs; Alcohol consumption; Non-fasting blood samples; Hospitalization; time of sampling; Acute infectious diseases.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method High-sensitivity c-reactive protein. Timepoint: Before the experiment, 12 weeks after the intervention. Method of measurement: biochemical measurements on blood sample.;Serum triglycerides. Timepoint: Before the experiment,12 weeks after the intervention. Method of measurement: biochemical measurements on blood sample.;High-density lipoprotein. Timepoint: Before the experiment, 12 weeks after the intervention. Method of measurement: biochemical measurements on blood sample.;Low-density lipoprotein. Timepoint: Before the experiment, 12 weeks after the intervention. Method of measurement: biochemical measurements on blood sample.;Total cholesterol. Timepoint: Before the experiment, 12 weeks after the intervention. Method of measurement: biochemical measurements on blood sample.
- Secondary Outcome Measures
Name Time Method Body Mass Index. Timepoint: Before the experiment, 12 weeks after the intervention. Method of measurement: Calculated according to the formula.;Weight. Timepoint: Before the experiment, 12 weeks after the intervention. Method of measurement: Electronic Scales.