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The effect of the transitional care program from hospital to own home using the digital messaging application on self-efficacy, quality of life, cardiac symptoms, and medication adherence among patients undergoing coronary artery bypass graft surgery and caregiving burden in their family caregivers

Not Applicable
Recruiting
Conditions
Coronary artery bypass graft surgery.
Atherosclerosis of coronary artery bypass graft(s) and coronary artery of transplanted heart with angina pectoris
I25.7
Registration Number
IRCT20180113038347N2
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
70
Inclusion Criteria

Inclusion criteria for patients: Age over 18 years
Performing coronary artery bypass graft (CABG) surgery for the first time in patients
No concomitant surgery during CABG surgery
Absence of respiratory diseases
Absence of drug and alcohol addiction
No history of seizures or mental health problems
No disturbance of consciousness or cognitive problems
Living with a family caregiver (spouse or children)
Have adequate health literacy
Having a smartphone
Ability to use WhatsApp
Conscious consent to participate in the study
Inclusion criteria for family caregivers: Age over 18 years
A close family member of the patient
Lack of a history of any mental health problems
Living with the patient
Have adequate health literacy
Having a smartphone
Ability to use WhatsApp
Ability to communicate effectively
The first experience of caring for a patient undergoing CABG surgery
Conscious consent to participate in the study

Exclusion Criteria

Exclusion criteria for patients: Patient dissatisfaction to continue working with the researcher
Re-hospitalization of the patient during the research
Patient death during the intervention
Exclusion criteria for family caregivers:
Dissatisfaction to continue working with the researcher
Patient death during the intervention

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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