Skip to content

Comparative Study of the Effect of peer group and Orientation Program on patients' Anxiety Before Coronary Artery Bypass Graft (CABG) Surgery

Comparative Study of the Effect of peer group and Orientation Program on patients' Anxiety Before Coronary Artery Bypass Graft (CABG) Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014102619677N1
Enrollment
150
Registered
2014-12-01
Start date
2014-10-21
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

cvd. Atherosclerotic heart disease

Interventions

Intervention 1: Intervention group1: peer group: In the peer group, patients are trained by someone who has a history of a successful coronary artery bypass graft (CABG) surgery for one hour. The edu
Intervention group1: peer group: In the peer group, patients are trained by someone who has a history of a successful coronary artery bypass graft (CABG) surgery for one hour. The education content i
Intervention group2: Orientation program: In orientation program group, this program is provided by the researcher for 30 minute to become the patients familiar with the equipments of the ICU and oper
Control group: In control group no intervention is provided and they only receive routine care of the units.

Sponsors

Ethics committee of Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria consist of: having CABG surgery for the first time; age more than 18 years old, being able to read and write; not having other serious physical and mental disorder; not having history of anxiety and depression and not using sedative drugs. The exclusion criteria are: not being consent to continue participation in the study; getting sick or not having normal homodynamic conditions during research.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: One day presurgery and one hour presurgery. Method of measurement: Spielberger state anxiety Inventory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHadi Nematian Jelodar

Mazandaran University of Medical Science

nematiyan_hadi@yahoo.com+98 11 3245 2384

Outcome results

None listed

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