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Evaluation of promoting healthy lifestyle program among individual at risk of cardiovascular diseases: An application of Health Behavior Model

Evaluation of promoting healthy lifestyle program among individual at risk of cardiovascular diseases: An application of Health Behavior Model

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017101625431N3
Enrollment
170
Registered
2017-11-08
Start date
2017-11-21
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

Cardiovascular disease. Cardiovascular disease, unspecified

Interventions

Intervention 1: Intervention group: Group intervention in five groups for five weeks includes training on blood pressure, blood glucose and health promotion behaviors in the intervention group based o
Lifestyle
Intervention group: Group intervention in five groups for five weeks includes training on blood pressure, blood glucose and health promotion behaviors in the intervention group based on the results of
Control group: The control group did not intervene and only blood pressure and blood glucose were measured twice weekly.

Sponsors

Vice chancellor for research, School of Public Health, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Major entry requirements: At least reading and writing literacy; Lack of severe depression; Mental and physical disability Major exclusion criteria: lack of consent to continue study by the person himself

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Age. Timepoint: Before intervention. Method of measurement: Questionnaire.;Eex. Timepoint: Before intervention. Method of measurement: Questionnaire.;Education. Timepoint: Before intervention. Method of measurement: Questionnaire.;Income. Timepoint: Before intervention. Method of measurement: Questionnaire.;Marital status. Timepoint: Before intervention. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Perceived sensitivity. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: Questionnaire.;Perceived severity. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: Questionnaire.;Perceived benefits. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: Questionnaire.;Perceived barriers. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: Questionnaire.;Guidance for practice. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: Questionnaire.;Self-sufficiency. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: Questionnaire.;Body mass index. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: BMI.;Smoking. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: Questionnaire.;Blood pressure. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: Blood Pressure Monitor.;Blood glucose. Timepoint: Before intervention, after intervention, three months after intervention. Method of measurement: Blood glucose meter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSohrab Babaei

Tehran University of Medical Sciences

sbabaei@razi.tums.ac.ir+98 21 7726 6553

Outcome results

None listed

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