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Effect of Diabetes Education by Peer Coaching on Diabetes Control and Management

Effect of Diabetes Education by Peer Coaching on Diabetes Control and Management

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201501128175N3
Enrollment
492
Registered
2015-09-18
Start date
2015-04-09
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

type 2 Diabetes. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: An unblinded randomized clinical trial in which women with type 2 diabetes are divided into one of the two following categories: • intervention group: diabetic patients who received ed
Lifestyle
An unblinded randomized clinical trial in which women with type 2 diabetes are divided into one of the two following categories: • intervention group: diabetic patients who received education through
An unblinded randomized clinical trial in which women with type 2 diabetes are divided into one of the two following categories: • control group: diabetic patients who received routine care includes

Sponsors

Endocrinology & Metabolism Research Institute of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
73 Years to 33 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria Individuals eligible for attending in the study are women with type 2 diabetes who have HbA1c = 8% in the last 6 months. Patients should not plan to migrate out of Tehran during the period of study and research team could easily have been in contact with them. Additionally, following criteria is essential: • Ability to speak in Persian • Age between 20 and 60 years old • To have HbA1c = 8% in the last 6 months • Not be pregnant • Patients with a life expectancy of less than a year and has a serious illness and disease with reduced cognitive capacity approved by the health center staff will be recruited. • Patients who are currently enrolled in a diabetes education programs are not included in the study. exclusion criteria • To have HbA1c equal and above 9% during the study • Become pregnant during the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
HbA1c. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: HPLC.

Secondary

MeasureTime frame
Fasting Blood Suger. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: Glocose Oxidase.;Total Cholestrol. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: CHOD-Pap.;Triglyseridi. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: Gpo-pap.;LDL. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: photometery.;HDL. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: photometery.;Body Mass Index. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: weight (kg) / height (m)2.;Blood Pressure. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: Manometer (mmhg).;Waist to Hip Ratio. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: waist hip ratio measurement.;Food intake. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: The three-day recall questionnaire.;Levels of physical activity. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: International Physical Activity Questionnaire (IPAQ.;Self-care activity. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: summery of diabetes self-care activities- SDSCA.;Quality of Life. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: Diabetes Quality of Life (DQOL) Questionnaire.;Depression. Timepoint: Before the intervention and at 3, 6 and 12 months after intervention. Method of measurement: Beck Depression Inventory.;Social Capital. Timepoint: Before the intervention and at 3, 6 and 12 months after interventi

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahnaz Sanjari

Endocrinology and Metabolism Research Institute Tehran University of medical Sciences,Tehran, Iran

emri-research@tums.ac.ir+98 21 8822 0088

Outcome results

None listed

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