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The effect peer support in the diabetes control Public title : The effect peer support in the diabetes control

Study effect of the peer support on self efficacy level in type II diabetic patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013080712974N2
Enrollment
80
Registered
2014-08-26
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 were supported by their peers in face to face meetings for 3 following months (10 sessions of 2
The control group received only routine care (such as the periodical doctor visits and pedagogical classes).
After preparing peers, the participants in the intervention group in the selected center were supported by their peers in face to face meetings for 3 following months (10 sessions of 2 hours) whit ins

Sponsors

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

Eligibility

Sex/Gender
All
Age
30 Days 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. 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
Self efficacy level. Timepoint: Before the intervention, three months after the intervention. Method of measurement: DMSES questionnaire.

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