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The effect of the DASH diet in patients with type 2 diabetes

The effect of DASH diet on lipid profile in type 2 diabetic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017021432571N1
Enrollment
80
Registered
2017-05-28
Start date
2016-01-20
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes mellitus. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: The intervention group will be adherence to DASH diet for a period of 12 weeks. Intervention 2: The control group will be adherence to American Diabetes Association recommendations f
Prevention
The intervention group will be adherence to DASH diet for a period of 12 weeks.
The control group will be adherence to American Diabetes Association recommendations for a period of 12 weeks.

Sponsors

Urmia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Criteria for inclusion in the study: Suffering from diabetes type 2; Not Suffering from any diabetic complications such as nephropathy, retinopathy, neuropathy and cardiovascular complications; Aged between 18 to 65; Consumption of same drugs (glibenclamide, metformin). Criteria for exclusion from the study: Suffering from diabetes type 1; Insulin Therapy; Suffering from liver diseases; Suffering from renal diseases; Suffering from thyroid disease; Pregnancy and lactation; Smoking and drinking alcohol; Consumption of drugs reducing blood fat and pressure and Weight, thiazide diuretics and corticosteroids; Change of type and dosage of consuming drugs during the study; Consumption of Herbal or chemical supplements; Suffering from Electrolyte abnormalities and Digestive diseases associated with malabsorption; Gastric bypass surgery and cholecystectomy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Total cholesterol. Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: enzymatic method, mg/dl.;Triglyceride. Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: enzymatic method, mg/dl.;HDL cholesterol. Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: enzymatic method, mg/dl.;LDL cholesterol. Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: enzymatic method, mg/dl.;VLDL cholesterol. Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: Triglyceride/5, if TG>400: VLDL-C = TC – (HDL-C + LDL-C), mg/dl.;Free Fatty Acid. Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: ELISA method, nmol/ml.;Weight. Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: Inbody770 Body Analyzer, kg.

Secondary

MeasureTime frame
Systolic blood pressure. Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: Mercury sphygmomanometer, mmHg.;Diastolic blood pressure. Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: Mercury sphygmomanometer, mmHg.;Body composition analysis (Fat mass, Fat free mass, Body water, Body cell mass, Skeletal muscle mass). Timepoint: Before Intervention and 12 weeks after Intervention. Method of measurement: Inbody770 Body Analyzer, Bioelectrical impedance analysis.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Manafi

Urmia University of Medical Sciences

majidmanafi@yahoo.com+44 1278803

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026