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The Effects of Intake of the Fortified Bread by Whey Protein Concentrate in Women With Type 2 Diabetes Mellitus

The Effects of Intake of the Fortified Bread by Whey Protein Concentrate on Glycemic Control, Lipid Profile, Blood Presure, Anthropometric Parameters, Resting Energy Expenditure, Oxidative Stress Markers and Appetite in Women With Type 2 Diabetes Mellitus

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110123005670N26
Enrollment
44
Registered
2019-01-07
Start date
2019-01-20
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

type 2 diabetes. Type 2 diabetes mellitus

Interventions

Intervention 1: Intervention group: About 120 g fortified whole bread by whey protein concentrate per day for 90 days. Intervention 2: Control group: About 120 g whole bread per day for 90 days.

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: Willingness to cooperation Women with type 2 diabetes mellitus Women aged 25-55 years glucose lowering tablets usage BMI= 25-35 kg/m2 GFR > 60 ml/min

Exclusion criteria

Exclusion criteria: Unwillingness to cooperation Patients with inflammatory, immunologic, psychologic, pulmonary, and neoplastic diseases Patients with renal, hepatic, and thyroid disorders Supplement intake Use of corticosteroids, non-steroidal anti-inflammatory, and hormonal drugs Change in type or dosage of used drugs during the study Change in diet and physical activity during the study Tobacco use Use of insulin Special physiologic conditions such as pregnancy, lactation, and menopause Patients with malabsorption diseases such as sprue and Crohn's disease Allergy or intolerance to milk components

Design outcomes

Primary

MeasureTime frame
Fasting Blood Glucose. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Enzymatic by commercial kits.;Insulin. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: ELISA.;Hemoglobin A1C. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: ELISA with commercial kits.;HOMA-IR. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Calculation.;Triglyceride. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Enzymatic.;HDL-Cholesterol. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Enzymatic.;MDA. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: spectrophotometry.;TAC. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: spectrophotometry.

Secondary

MeasureTime frame
Blood Pressure. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Digital Barometer.;Weight. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Scale.;Body Mass Index (BMI). Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Computing.;Body fat percent. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Bio impedance set.;Waist circumference. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: measurement by meter.;Hip circumference. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: measurement by meter.;WHR. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Computing.;Appetite. Timepoint: Before the intervention and 90 days after the start of the intervention. Method of measurement: Appetite Assessment Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ali Tarighat-Esfanjani

Tabriz University of Medical Sciences

Tarighata@tbzmed.ac.ir+98 41 3336 2117

Outcome results

None listed

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