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Effect of peer education on fear, anxiety and depression of patients undergoing coronary angiography

Effect of Peer education on fear, anxiety and depression of Patient under going coronary angiography

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201508028124N4
Enrollment
70
Registered
2016-07-29
Start date
2016-02-20
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

Coronery Heart Disease. Atherosclerotic Heart Disease

Interventions

Intervention 1: in the experimental group, Patient receive education of care before and after angiography, one meeting, during 30-45 minute, 3 hours before of Procedure by peer who has a successful hi
in the experimental group, Patient receive education of care before and after angiography, one meeting, during 30-45 minute, 3 hours before of Procedure by peer who has a successful history of angiogr
participants of control group received routine oral instructions: to be NPO, to shave, and how to take the drugs and cut Anti coagulation drug..

Sponsors

vice chancellor for research, Shiraze University of Medical Scienses
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 25 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: Age limit of 30 to 70; Lack of psychological disorder and psychological therapy on the basis of a psychologist advice; Lack of previous angioplasty; Lack of any types of cognitive, speech and hearing disorders lack of pain during of the teaching; A complete consent to participate in the survey. Exclusion criteria:The incidence of sharp deterioration in the ailment.; The elimination of those who face critical conditions consist of chest pain, body problem for example headach, vertigo, nausea, vomiting and Hemodynamic problem for example chenge of BP ... mental problem and another condition that result of lack of particepation during the survey ,the Patient of dureng techeang are not attend the contenue in particepation of study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fear. Timepoint: Before intervention and After intervention. Method of measurement: VAS.;Anexiety. Timepoint: Before intervention and After intervention. Method of measurement: DAS-21.;Depression. Timepoint: Before intervention and After intervention. Method of measurement: DAS-21.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Shahabfard

Shiraz University of Medical Sciences,Hazrate Fatemeh Nursing and Midwifery Faculty

shahabfard59@gmail.com+98 71 3647 4257

Outcome results

None listed

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