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The Effect of TUBER Recommendations and the DASH Diet on Blood Parameters in Patients With Gestational Diabetes

The Effect of TUBER Recommendations and the DASH Diet on Blood Parameters in Patients With Gestational Diabetes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07101406
Enrollment
38
Registered
2025-08-03
Start date
2024-06-01
Completion date
2025-07-22
Last updated
2025-08-07

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

Conditions

Gestational Diabetes Mellitus (GDM), Gestational Diabetes Mellitus in Pregnancy, Diet- Controlled

Keywords

gestational diabetes, dash diet, Türkiye Nutrition Guide, diet

Brief summary

The aim of this clinical trial was to examine the effects of the Turkish Nutrition Guide Recommendations Diet and the DASH Diet on blood sugar, blood pressure, and biochemical parameters in patients with gestational diabetes. The study hypotheses are as follows: Hypothesis 1: The DASH diet reduces fasting blood glucose levels more in patients with gestational diabetes compared to a diet adapted to a healthy diet specific to Türkiye. Hypothesis 1: The DASH diet reduces insulin levels more in patients with gestational diabetes compared to a diet adapted to a healthy diet specific to Turkey. Hypothesis 1: The DASH diet reduces HbA1c levels more in patients with gestational diabetes compared to a diet adapted to a healthy diet specific to Türkiye. Hypothesis 1: The Dash diet reduces 1st-hour postprandial glucose levels more significantly in women with gestational diabetes compared to a diet adapted to a healthy diet typical of Türkiye. Participants: After being diagnosed with gestational diabetes by a doctor using an OGTT test at 24-28 weeks, the researcher will complete a general information form during their first consultation with the dietitian. For four weeks, the dietitian will follow the diets created by the researcher based on their assigned diet group in a blinded manner. They will record their fasting and postprandial blood sugar levels in the morning, noon, evening, night, and during snacks, if they are taking them. They will keep a 24-hour food consumption record before meeting with the researcher weekly. Participants will have their biochemical parameters assessed at the beginning of the study and at the end of the fourth week.

Interventions

OTHERTürkiye Nutrition Guideline Diet

A diet structured according to the Türkiye Nutrition Guideline (TÜBER) for pregnant women, consisting of 45-60% carbohydrates, 12-20% protein (minimum 70 g), and 20-35% fat. Diets were tailored weekly based on blood glucose levels and individual dietary intake records.

OTHERDASH Diet

A dietary plan based on DASH guidelines: 45-60% carbohydrates (≥175 g), 12-20% protein (≥70 g), 20-35% fat (≤6% saturated), ≤2300 mg sodium, ≥4700 mg potassium, ≥1250 mg calcium, ≥500 mg magnesium. Includes low-fat dairy, lean meats, fruits/vegetables, and nuts/seeds.

Sponsors

Kardelen Kandemir
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Randomized single-blind. Participants were blinded.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Female participants aged 18 to 35 years * Singleton pregnancy * Clinical diagnosis of gestational diabetes mellitus (GDM) * Ability to use a glucometer

Exclusion criteria

* Pre-gestational diabetes or impaired glucose tolerance (IGT) * Hypoglycemia * Receiving insulin therapy * Development of preeclampsia * Failure to adhere to the prescribed diet * Smoking * Alcohol consumption

Design outcomes

Primary

MeasureTime frameDescription
Change in fasting blood glucose levelsDaily for 4 weeksTo monitor daily fasting blood glucose levels (mg/dL) using a glucometer throughout the 4-week intervention.

Secondary

MeasureTime frameDescription
Change in fasting insulin levelBaseline and Week 4To evaluate changes in fasting insulin levels (µIU/mL) from baseline to the end of the 4-week intervention period.
Change in daily energy and nutrient intake based on 24-Hour Food Consumption RecordBaseline and weekly over 4 weeksTo assess participants' dietary intake patterns and nutrient adequacy by analyzing the 24-Hour Food Consumption Record collected at baseline and during follow-up. The analysis includes total daily energy intake (kcal) and macronutrient (carbohydrates, protein, fat) and micronutrient (iron, folic acid, vitamin D, etc.) intake levels. Energy: kcal/day Macronutrients: grams/day (carbohydrates, protein, fat) Micronutrients: mg or µg/day (iron, folic acid, vitamin D, etc.)
Change in lipid profile (total cholesterol, HDL-C, LDL-C, triglycerides)Baseline and Week 4To evaluate the effect of the dietary intervention on lipid metabolism by measuring changes in total cholesterol, HDL cholesterol, LDL cholesterol (direct measurement), and triglyceride levels from baseline to week 4. Each parameter will be analyzed individually and reported in mg/dL. Total cholesterol (mg/dL) HDL cholesterol (mg/dL) LDL cholesterol - direct measurement (mg/dL) Triglycerides (mg/dL)
Change in 1-hour postprandial blood glucose levelsDaily for 4 weeksTo track 1-hour post-meal blood glucose levels (mg/dL) recorded daily throughout the study.
Change in vitamin and hematological markers (Vitamin D, folic acid, hemoglobin, hematocrit)Baseline and Week 4To evaluate changes in nutritional and hematological status from baseline to the end of the intervention period. 25-OH vitamin D: mcg/L Folic acid: mcg/dL Hemoglobin: g/dL Hematocrit: %
Change in HbA1c levelBaseline and Week 4To assess the effect of the dietary intervention on long-term glycemic control by measuring HbA1c levels (%) before and after the intervention.
Change in iron-related parameters (iron, ferritin, total iron-binding capacity)Baseline and Week 4To assess the effect of the intervention on iron status by measuring serum iron, ferritin, and total iron-binding capacity (TIBC) at baseline and Week 4. Iron: mcg/dL Ferritin: mcg/L TIBC: mcg/dL

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026