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Assessing the Effect of Educational Intervention in metabolic indices of diabetic patients

Assessing the Effect of Educational Intervention Based on Health Belief Model in improving metabolic indices of type2 diabetic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170619034641N2
Enrollment
50
Registered
2017-12-28
Start date
2017-12-22
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 due to underlying condition

Interventions

Intervention 1: Intervention group: educational intervention will be conducted weekly during 6 sessions (60 minutes) with a designed program according to the Health Belief Model. this intervention wi
Lifestyle
Intervention group: educational intervention will be conducted weekly during 6 sessions (60 minutes) with a designed program according to the Health Belief Model. this intervention will be implemente
Control group: The control group receives only routine training during this time.

Sponsors

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Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria include: at least one year have passed from a definitive diagnosis of type 2 diabetes, being in the age group of 30 to 65 years old, their HbA1c test is equal or higher than 7% and no perceptual problem.

Exclusion criteria

Exclusion criteria: Exclusion criteria include: patients who do not attend more than one session in the educational intervention, patients who do not perform the required tests completely and Patients who are not willing to cooperate in the study anyway.

Design outcomes

Primary

MeasureTime frame
Glycated haemoglobin (HbA1c). Timepoint: Before the intervention and three months after the intervention. Method of measurement: A1C care device.;Fasting blood sugar (FBS). Timepoint: Before the intervention and three months after the intervention. Method of measurement: AutoAnalyzer.;Triglyceride (TG). Timepoint: AutoAnalyzer. Method of measurement: AutoAnalyzer.;Cholesterol. Timepoint: Before the intervention and three months after the intervention. Method of measurement: AutoAnalyzer.;High-density lipoprotein (HDL). Timepoint: Before the intervention and three months after the intervention. Method of measurement: AutoAnalyzer.;Low-density lipoprotein (LDL). Timepoint: Before the intervention and three months after the intervention. Method of measurement: AutoAnalyzer.;Perceived Susceptibility. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Health belief model researcher-made questionnaire.;Perceived Severity. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Health belief model researcher-made questionnaire.;Perceived Barriers. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Health belief model researcher-made questionnaire.;Perceived Benefits. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Health belief model researcher-made questionnaire.;Cues to action. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Health belief model researcher-made questionnaire.;Self-efficacy. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Health belief model researcher-made questionnaire.;Body mass index (BMI). Timepoint: Before the intervention and three months after the intervention. Method of measurement: DETECTO-MEDIC Height and Weight Measurement Device.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactalireza abdi

Kermanshah School of Nursing and Midwifery

arabdi@kums.ac.ir+98 83 3835 8258

Outcome results

None listed

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