Investigating the effect of lifestyle education using mobile application on the treatment plan of patients with hypertension

The effect of lifestyle education using a mobile application for the treatment of patients with hypertension referred to the health center of Zarrin Abad in 2021-2022

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220521054948N1

Enrollment

Registered

2022-07-12

Start date

2022-07-06

Completion date

Unknown

Last updated

2022-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertensive disease. Hypertensive heart disease

Interventions

Intervention 1: Intervention group: The intervention of group one, in addition to the usual treatment, will be an educational-supportive intervention (usual care plus intervention) through a software

Eligibility

Sex/Gender

All

Age

30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the study Definitive diagnosis of hypertension (equal to or greater than 90.140 mm Hg, 3 times a day) and at least one month after the onset of hypertension Systolic and diastolic blood pressure equal to or greater than 90.140 mm Hg Having a mobile phone with the ability to install software Ability to work with software in the patient or a family member to use the software (such as vision and the ability to work with hands, having the ability to work with mobile phones at least at the beginner level Familiarity with Persian language (reading, writing and speaking) yourself or a family member Do not suffer from neurological diseases and learning disorders No other chronic diseases such as stroke, crippling diseases (multiple sclerosis, Guillain-Barré syndrome), dialysis, cardiomyopathy, malignant tumors and pregnancy

Exclusion criteria

Exclusion criteria: Reluctance to continue cooperation in research Occurrence of other diseases requiring therapeutic intervention during the study

Design outcomes

Primary

Measure	Time frame
Adherence to the treatment plan of patients with hypertension. Timepoint: Before intervention - two months after intervention. Method of measurement: Researcher-made questionnaire on adherence to treatment regimen.;Blood pressure. Timepoint: Before the intervention and at each visit - the pressures recorded in the software. Method of measurement: Mercury sphygmomanometer.;Lifestyle training. Timepoint: Before intervention - two months after intervention. Method of measurement: Questionnaire developed by the researcher on treatment compliance.;Regular monitoring of blood pressure. Timepoint: Every other day. Method of measurement: Registration in the software.	—

Measure

Time frame

Adherence to the treatment plan of patients with hypertension. Timepoint: Before intervention - two months after intervention. Method of measurement: Researcher-made questionnaire on adherence to treatment regimen.;Blood pressure. Timepoint: Before the intervention and at each visit - the pressures recorded in the software. Method of measurement: Mercury sphygmomanometer.;Lifestyle training. Timepoint: Before intervention - two months after intervention. Method of measurement: Questionnaire developed by the researcher on treatment compliance.;Regular monitoring of blood pressure. Timepoint: Every other day. Method of measurement: Registration in the software.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyedeh Zahra Karami

Islamic Azad University

www.zahrakarami1374@gmail.com+98 21 2660 2642

Outcome results

None listed

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