Comparing the effect of educational film with the routine education about blood glucose controlling in type 2 diabetic patients

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT2013121515797N1

Enrollment

120

Registered

2014-03-03

Start date

2014-02-20

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: Intervention group: presentation of educational film in type 2 diabetic patients with question and answer. Intervention 2: Control group: routine education in diabetes center.

Intervention group: presentation of educational film in type 2 diabetic patients with question and answer

Control group: routine education in diabetes center

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria :Type 2 diabetic patients that referred to the Hamadan diabetes center; Volunteered to participate in the study; History of type 2 diabetes two years ago Exclusion criteria: absence in movie section; Not complete the questionnaire

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Knowledge. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Perceived susceptibility. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Perceived severity. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Perceived benefits. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Perceived barriers. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Cues to action. Timepoint: Before and after intervention. Method of measurement: Questionnaire.	—

Measure

Time frame

Knowledge. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Perceived susceptibility. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Perceived severity. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Perceived benefits. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Perceived barriers. Timepoint: Before and after intervention. Method of measurement: Questionnaire.;Cues to action. Timepoint: Before and after intervention. Method of measurement: Questionnaire.

—

Secondary

Measure	Time frame
HbA1C. Timepoint: 3 month after intervention. Method of measurement: Blood test.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Mohammad Mahdi Hazavehei

Hamadan University of Medical Sciences

hazavehei@umsha.ac.ir+98 81 1838 1641

Outcome results

None listed

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