Skip to content

The effect of the education on adherence

The effect of the educational program on adherence of patients with high blood pressure

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014070117237N4
Enrollment
96
Registered
2015-08-15
Start date
2015-07-03
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

Hypertention. Essential (primary) hypertension

Interventions

Intervention 1: Intervention group: Two hours face to face education based on lifestyle modification guideline will be done twice a week for two weeks. Intervention 2: Control group: without any inte
Intervention group: Two hours face to face education based on lifestyle modification guideline will be done twice a week for two weeks.

Sponsors

Vice Chancellor for research of Golestan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age from 18 to 65 years; having the ability to read and write; having Systolic Blood Pressure more than 140 and less than 169; having Diastolic Blood Pressure more than 90 and less than 109; at least 6 months history of treatment; having complete alertness; hearing and speech ability; don't be pregnant during participating in study; not having known psychiatric disorders; don't have chronic illness such as cancer, lupus, advanced heart failure, ARDS, CVA and diabetes; not using opium or alcohol. Exclusion criteria: don't want to continue participation; travel or migration during study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Adherennce. Timepoint: Before intervention and two weeks after intervention. Method of measurement: Using checklist to measur adrerenct to treatment in diets, excercise and drug.

Secondary

MeasureTime frame
Level of blood pressure. Timepoint: Before intervention and two weeks after intervention. Method of measurement: Using sphygmomanometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtharAlsadat Mirkarimi

Golestan University of Medical Sciences

e.mirkarimi@gmail.com+98 17 3242 6900

Outcome results

None listed

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