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Comparison effect of peer education and orientation tour on stress and anxiety of patients candidates for coronary angiography

Comparison the effect of peer education and orientation tour on anxiety and stress of patients candidate for coronary angiography in selected hospital of AJA University of Medical Sciences

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014032617086N1
Enrollment
177
Registered
2014-08-31
Start date
2014-06-15
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

Chronic ischemic heart disease. Atherosclerotic heart disease

Interventions

Intervention 1: The orientation tour, samples of study, are trained in the form of a 30 to 40 minute tour In the angiography ward . Intervention 2: In peer education group, the subjects are trained wi
The orientation tour, samples of study, are trained in the form of a 30 to 40 minute tour In the angiography ward .
In peer education group, the subjects are trained within one hour by a peer who has a successful history of angiography.

Sponsors

Aja University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1.Angiography should be performed for the first time and not have a history of cardiac hospitalization. 2. Angiography is not the type of emergency. 3. All participants must be able to read and write. 4. In the past are not under other invasive procedures such as transesophageal echocardiography. 5. A history of heart valve disease are not known. 6. Do not have cognitive problems and physical disability. 7. Do not have a history of depression and anxiety and use of sedative drugs. 8. Aged from 25 to 65 years old. 9. They are not a member of the medical staff. 10. One of their relatives are not Coronary angiography previously. Exclusion criteria: 1. If patients are clinically ill and have not stable condition hemodynamically. 2. Sedative drugs apart from routine drug given to all patients be prescribed. 3. The patient does not want to continue participating in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Hospitalization day (one day before the procedure and before the intervention), two hours before angiography (the day after intervention). Method of measurement: DASS-21 questionnaire.;Stress. Timepoint: Before intervention (day before the angiography) and after intervention (two hours before the procedure). Method of measurement: DASS-21 questionnaire.

Secondary

MeasureTime frame
Vital signs except temperature. Timepoint: Before intervention (day before the angiography) and after intervention (two hours before the angiography). Method of measurement: Sphygmomanometer and stethoscope.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Eslami

Aja University of Medical Sciences

Slami90@ymail.com+98 21 7750 0404

Outcome results

None listed

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