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The Effect of Educational Intervention on Asprosin Levels and Insulin Resistance in Diabetic Patients

Investigating the efficacy of Self-Care Educational Intervention on Asprosin Levels and Insulin Resistance in Type 2 Diabetes Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160625028627N5
Enrollment
88
Registered
2025-06-09
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-07-21

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

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Iranian nationality Age 18 years and above Diagnosed with type 2 diabetes for at least 6 months Glycated hemoglobin level of 8% or higher

Exclusion criteria

Exclusion criteria: Complications of type 2 diabetes that disrupt the patient's care process, such as blindness, dialysis, severe stroke Medical history of cognitive disorders like dementia or Alzheimer's Uncontrolled hypertension above 180/110 millimeter of mercury Hearing and visual impairments Hemolytic anemia Hemoglobinopathy

Design outcomes

Primary

MeasureTime frame
Asprosin. Timepoint: Evaluation of Mean Asprosin Levels (nanogram per milliliter) Before the Intervention and 3 Months After the Completion of the Intervention. Method of measurement: Blood test using ELISA kit.;Insulin resistance. Timepoint: Assessment of insulin resistance before the intervention and 3 months after the completion of the intervention. Method of measurement: Blood test using ELISA kit (HOMA-IR index).

Secondary

MeasureTime frame
Mean serum BUN levels (milligrams per deciliter). Timepoint: Mean serum BUN levels (milligrams per deciliter) before the intervention and 3 months after the completion of the intervention. Method of measurement: Blood test using enzymatic kit with urease-glutamate dehydrogenase (GLDH) method.;Body mass index. Timepoint: Mean Body mass index levels (kilogram per square meter) before the intervention and 3 months after the completion of the intervention. Method of measurement: Measurements will be performed by trained staff using calibrated digital scales and stadiometers.;Mean changes in systolic blood pressure (millimeter of mercury). Timepoint: Mean systolic blood pressure levels (millimeters of mercury) before the intervention and 3 months after the intervention. Method of measurement: Calibrated digital sphygmomanometer.;Mean changes in diastolic blood pressure (millimeters of mercury). Timepoint: Mean diastolic blood pressure levels (millimeters of mercury) before the intervention and 3 months after the intervention. Method of measurement: Calibrated digital sphygmomanometer.;Mean serum triglyceride levels (milligrams per deciliter). Timepoint: Mean Serum triglyceride levels (milligrams per deciliter) before the intervention and 3 months after the completion of the intervention. Method of measurement: Blood test using enzymatic colorimetric assay kits.;Mean serum total cholesterol levels (milligrams per deciliter). Timepoint: Mean serum total cholesterol levels (milligrams per deciliter) before the intervention and 3 months after the completion of the intervention. Method of measurement: Blood test using enzymatic colorimetric assay kits.;Mean serum LDL-C levels (milligrams per deciliter). Timepoint: Mean serum LDL-C levels (milligrams per deciliter) before the intervention and 3 months after the completion of the intervention. Method of measurement: Blood test using direct enzymatic assay kits.;Mean serum HDL-C levels (milligrams per deciliter). Timepoint: Mean

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Golnaz Azami

Sanandaj University of Medical Sciences

golnaz.azami64@gmail.com+98 87 3366 4664

Outcome results

None listed

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