The effect of peer education on medication adherence and quality of life of clients with hypertension. The effect of peer education on medication adherence and quality of life of clients with hypertension. The effect of peer education on medication adherence and quality of life of clients with hypertension.

The effect of peer education on medication adherence and quality of life of clients with hypertension. The effect of peer education on medication adherence and quality of life of clients with hypertension.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016102629809N1

Enrollment

110

Registered

2016-10-26

Start date

2016-06-04

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. Hypertensive diseases

Interventions

Intervention 1: This study selected peer group and their educational and intervention phase begins on patients in experimental group patients in the test group are In addition to training routine, one

Behavior

This study selected peer group and their educational and intervention phase begins on patients in experimental group patients in the test group are In addition to training routine, one-hour sessions o

Patients who are in control group receive the routine training that includes training by a doctor and receive using posters in the clinic.

Eligibility

Sex/Gender

All

Age

15 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: at least six months have passed by physician diagnosis of blood pressure; patients with primary hypertension are filled; have aged 15 years old and older; history of participation in training programs in the field of medication adherence and blood pressure during the past six months alone; at least one blood pressure medication taken by the patient; literate and have the ability to speak the Persian language; cognitive difficulties, physical disability does not have; employment or education in related groups, not medical. Exclusion criteria: treatment regimen (medication adherence) patient change; patients during the study in collaboration with researcher has revised and happy to be working; to participate in at least one of the training sessions held by counterparts have; disturbed that the new body will lose its ability to self-care; patients died during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Medication adherence. Timepoint: Two months after the intervention. Method of measurement: Morisky medication adherence questionnaire.;Quality of life. Timepoint: Two months after the intervention. Method of measurement: SF-36 questionnaire.	—

Secondary

Measure	Time frame
Hypertention. Timepoint: Two month after intervention. Method of measurement: Measurement of blood pressure, blood pressure measurement device is mercury.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDaryadokht masroor

School of Nursing and Midwifery, Iran University of Medical Sciences and Health Services

masror.d@iums.ac.ir+98 21 4365 1709

Outcome results

None listed

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