Skip to content

The effect peer support in the diabetes control

Study effect of the peer support on glycosylated hemoglobin level in type II diabetic patients.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013041012974N1
Enrollment
60
Registered
2013-08-20
Start date
2013-06-22
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

Diabetes. Diabetes mellitus

Interventions

Intervention 1: After preparing peers, the participants in the intervention group in the selected center are supported by their peers in face to face meetings for 3 following months (10 sessions of 2
Prevention
After preparing peers, the participants in the intervention group in the selected center are supported by their peers in face to face meetings for 3 following months (10 sessions of 2 hours)whit Instr
the control group receive only routine care (such as the periodical doctor visits and pedagogical classes).

Sponsors

Vice Chancellor for research, Tehran Islamic Azad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: The major eligibility criteria: They include the age (above 30); a primary literacy; the lack of physical limitations for self-care. Before entering the study; their hemoglobin A1C should be higher than normal; with a medical profile in the diabetes clinic; having a history of diabetes type 2 at least for one year; having sufficient time to participle in the group sessions.The major outcome criteria: The Lack of mental health and physical health relating to the age that may hinder the learning; such as memory problems; Alzheimer's; etc. the use of the medicines that affect the consciousness and learning levels. The affection to other known chronic diseases such as kidney; autoimmunization diseases etc. Based on the patients’ own statements; medical and paramedical educations; the intention of immigration during the study and the background of similar study participation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hemoglobin glycoside. Timepoint: Before the intervention, three months after the intervention. Method of measurement: Based on percent with get blood samples.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRashidi Kobra

Lorestan University of Medical Sciences (School of Nursing Boroujerd

krashidi2010@yahoo.com+98 66 2446 7452

Outcome results

None listed

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