The effect of the? designed ?transitional care plan from the Open Heart Intensive Care Unit to the general ward in patients undergoing coronary artery bypass graft surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20100531004062N2

Enrollment

Registered

2021-08-02

Start date

2021-09-23

Completion date

Unknown

Last updated

2021-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transitional care program for patients undergoing coronary artery bypass graft surgery from the open heart intensive care unit to the general ward. Atherosclerosis of coronary artery bypass graft(s) and coronary artery of transplanted heart with angina pectoris

Interventions

Intervention 1: Intervention group: after the necessary explanations to the ?research samples and obtaining informed consent, before ?transferring the patient from the open heart surgery-intensive ?ca

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients undergoing Coronary artery bypass graft(CABG) surgery who are candidates for transfer from the Open Heart Intensive Care Unit (OH-ICU) to the general ward at least two days after surgery as directed by the physician Level of consciousness 15 according to Glasgow Coma Scale (GCS) No chronic progressive disease or acute unpredicted complications of surgery No history of diagnosed psychological disorders

Exclusion criteria

Exclusion criteria: Reluctance to continue participating in the study during the intervention Death of the patient The occurrence of an unpredictable accident that interferes with the implementation of the program

Design outcomes

Primary

Measure	Time frame
Patients Satisfaction. Timepoint: After the intervention. Method of measurement: Patients Satisfaction Instrument.;Family Satisfaction. Timepoint: After the intervention. Method of measurement: Family Satisfaction Questionnaire.;Anxiety. Timepoint: Before and after the intervention. Method of measurement: Speilberger State – Trait Anxiety Inventory (STAI-Y)?.;Relocation Stress Syndrome. Timepoint: After the intervention. Method of measurement: Relocation Stress Syndrome Scale.;Total Comfort Score. Timepoint: Before and after the intervention. Method of measurement: Visual Analog Scale to Total Comfort.	—

Measure

Time frame

Patients Satisfaction. Timepoint: After the intervention. Method of measurement: Patients Satisfaction Instrument.;Family Satisfaction. Timepoint: After the intervention. Method of measurement: Family Satisfaction Questionnaire.;Anxiety. Timepoint: Before and after the intervention. Method of measurement: Speilberger State – Trait Anxiety Inventory (STAI-Y)?.;Relocation Stress Syndrome. Timepoint: After the intervention. Method of measurement: Relocation Stress Syndrome Scale.;Total Comfort Score. Timepoint: Before and after the intervention. Method of measurement: Visual Analog Scale to Total Comfort.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahar Khoshkesht

Tehran University of Medical Sciences

khoshkesht@razi.tums.ac.ir+98 21 6105 4000

Outcome results

None listed

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