Effectiveness of Education Interventional base on Extended Health Belief Model to Antiretroviral adherence in HIV/AIDS patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017020432386N1

Enrollment

Registered

2017-10-20

Start date

2016-10-22

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

Aids. Acute HIV infection syndrome

Interventions

Intervention 1: In the intervention group, 3 training sessions were held. The first session was for an hour and about the immune system's function. The second session was for an hour and about the gen

In the intervention group, 3 training sessions were held. The first session was for an hour and about the immune system's function. The second session was for an hour and about the general AIDS. The t

no intervention in control group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Entry criteria The drug recceived less than 23 time in the last 2 years; Willingness to participate in this research project; No prison record in the past two years; Treatment began more than two years Exit criteria any reason that a person is not able to cooperate during the study and conviction to prison during the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Adherece to Antiretroviral Treatment. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.	—

Secondary

Measure	Time frame
Social Suport. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Susceptibility. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Severity. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Barriers. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Benefites. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Self efficacy. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.	—

Measure

Time frame

Social Suport. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Susceptibility. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Severity. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Barriers. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Benefites. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.;Perceived Self efficacy. Timepoint: One month befor intervention and 3 month after. Method of measurement: Questionnaire.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJavad Yadegari

Qom University of Medical Science

jyadegari@muq.ac.ir+98 25332303387

Outcome results

None listed

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