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DASH diet in diabetes complications

The effect of Dietary Approaches to Stop Hypertension (DASH) diet on mental health, sleep, sexual hormones and advanced glycated end products (AGEs) serum levels among type 2 diabetic women: A clinical trial study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180312039055N1
Enrollment
60
Registered
2018-05-20
Start date
2018-05-22
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Condition 1: Depression. Condition 2: Diabetes. Condition 3: sleep.

Interventions

Intervention 1: Intervention group: Postmenopausal diabetic patients who adhere to the DASH diet. Intervention in this group of people receiving the DASH diet as a diet rich in antioxidants for three

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Tendency to participate in the study Patients with type 2 diabetes Postmenopause individuals (who don't have the period cycle for 12 months) Persons who dont adhere special diets

Exclusion criteria

Exclusion criteria: Patients with cancer, kidney, liver, heart and other specific diseases, patients with depression and other psychological diseases, New events which impact on patients mood Consumption of OCPs, hormonal supplements and hormone therapy Esterogen therapy during 3 last months Smoking Insulin therapy Consumption of supplements and vitamins during 2 last months Patients with depression and other psychological diseases, New events which impact on patients mood

Design outcomes

Primary

MeasureTime frame
Luteinizing Hormone (LH). Timepoint: Before and after intervention (12wk). Method of measurement: Serum levels by ELISA.;Follicle Stimulating Hormone (FSH). Timepoint: Before and after intervention (12wk). Method of measurement: Serum levels by ELISA.;Sex Hormone Binding Globulin (SHBG). Timepoint: Before and after intervention (12wk). Method of measurement: Serum levels by ELISA.;Testestrone. Timepoint: Before and after intervention (12wk). Method of measurement: Serum levels by ELISA.;Advanced Glycation End products (AGEs). Timepoint: Before and after intervention (12wk). Method of measurement: Serum levels by ELISA.;Depression. Timepoint: Before and after intervention (12wk). Method of measurement: DASS-21 item questionnaire.;Sleep status. Timepoint: Before and after intervention (12wk). Method of measurement: Pittsburgh sleep questionnaire index (PSQI).;Anxiety. Timepoint: Before and after intervention (12 wk). Method of measurement: DASS-21 item questionnaire.;Stress. Timepoint: Before and after intervention (12 wk). Method of measurement: DASS-21 item questionnaire.

Secondary

MeasureTime frame
Weight. Timepoint: Before and after intervention (12 wk). Method of measurement: Scale.;Waist circumference. Timepoint: Before and after intervention (12 wk). Method of measurement: inflexible meter.;Blood pressure. Timepoint: Before and after intervention (12 wk). Method of measurement: Digital Sphygmomanometer.;Body Mass Index (BMI). Timepoint: Before and after intervention (12 wk). Method of measurement: Weight in kilogram divided to square of height in meter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Leila Azadbakht

Tehran University of Medical Sciences

azadbakhtleila@gmail.com+98 21 8895 5975

Outcome results

None listed

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