The effect of smartphone-based monitoring and follow-up program on the quality of life and pain of patients undergoing coronary artery bypass graft surgery

Investigating the effect of smartphone-based monitoring and follow-up program implementation on the quality of life and pain of patients undergoing coronary artery bypass graft surgery

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240426061574N1

Enrollment

Registered

2024-06-05

Start date

2024-06-04

Completion date

Unknown

Last updated

2024-06-24

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

Conditions

Undergoing coronary artery bypass surgery.

Interventions

Intervention 1: Intervention Group: Actions for the intervention group during the three stages of the research: -Primary level

Developing a multimedia educational package for coronary artery bypass surgery: A multimedia educational package will be developed before the study begins. The educational package will be developed an

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Willingness to participate in the study Having awareness and mental health Coronary artery transplant surgery for the first time Non-emergent coronary artery bypass graft surgery Not having a history of mental disorder The patient herself or her active companion should be literate The patient herself or her active companion should have a smartphone and the possibility of using the internet for the patient or her companion within 30 days after the leave.

Exclusion criteria

Exclusion criteria: Addiction to drugs such as opium, which makes it difficult to feel pain and control it.

Design outcomes

Primary

Measure	Time frame
Quality of life. Timepoint: Pre-test stage: before surgery and during admission; Post-test stage: 30 days after discharge from the hospital. Method of measurement: The 36-Item Short Form Survey (SF-36) to measure Quality of Life.;Pain. Timepoint: Basic pain control in the preoperative phase; In the stage after discharge from the intensive care unit until discharge from the hospital, pain control three times a day in person; In the phase after discharge up to 30 days later, pain control in the form of phone calls on days 7, 14, 21 and 30. Method of measurement: Visual Analogue Scale.	—

Measure

Time frame

Quality of life. Timepoint: Pre-test stage: before surgery and during admission; Post-test stage: 30 days after discharge from the hospital. Method of measurement: The 36-Item Short Form Survey (SF-36) to measure Quality of Life.;Pain. Timepoint: Basic pain control in the preoperative phase; In the stage after discharge from the intensive care unit until discharge from the hospital, pain control three times a day in person; In the phase after discharge up to 30 days later, pain control in the form of phone calls on days 7, 14, 21 and 30. Method of measurement: Visual Analogue Scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Bakhshi

Yazd University of Medical Sciences

fateme.bakhshii@gmail.com+98 35 1751 3824

Outcome results

None listed

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