Discharge Planning Program for Post CABG Patients

NCT04527822 | Enrolling By Invitation DMC

• 1 other identifier: 101271-2
• Study Type: interventional
• Target: 174
• Locations: 1 country
• Sites: 1

Brief Summary

The current study is utilizing a nurse led discharge program based on the Re-Engineered Discharge program (Project-RED) ( Agency of Healthcare Research and Quality \[AHRQ\], 2013) which is a package of services designed to minimize discharge failures and minimize re-admissions, reduce mortality, morbidity, complication and improve patients outcomes. Project-RED aims to reduce hospital re-admissions through a series of structured steps led by a nurse called discharge advocate. The intervention will be used to discharge patients post Coronary artery bypass graft surgery.

Conditions

Coronary Artery Bypass Graft Surgery; Mace; 30 Day Mortality

Keywords

Coronary artery bypass graft surgery CABGl; MACE; nursing care

Outcome Measures

Primary Outcomes (1)

• Major adverse cardiovascular and cerebrovascular events

  The variable of MACCE includes MI, Stroke, and all-cause death and repeat re-vascularization

  30 days

Secondary Outcomes (1)

• Adherence to medications

  3 months

Study Arms (2)

Discharge planning program

EXPERIMENTAL

a discharge planning program. It is a modified discharge planning program depends basically on the Re-Engineered Discharge program which is a program developed by Boston Medical Center in collaboration with AHRQ , 2013. The intervention consists of several components. The program components include making appointments for follow-up care (e.g., medical appointments and post discharge tests/labs). Plan for the follow-up of results from tests or labs that are pending at discharge. Identify the correct medicines and a plan for the patient to obtain them. Teach a written discharge plan the patient can understand. Educate the patient about his or her diagnosis and medicines. Review with the patient what to do if a problem arises. Assess the degree of the patient's understanding of the discharge plan and provide a telephone reinforcement of the discharge plan

Other: Nurse led discharge planning program

Standard Care

ACTIVE COMPARATOR

Other: Nurse led discharge planning program

Interventions

Nurse led discharge planning program OTHER

a discharge planning program. It is a modified discharge planning program depends basically on the Re-Engineered Discharge program which is a program developed by Boston Medical Center in collaboration with AHRQ , 2013. The intervention consists of several components. The program components include making appointments for follow-up care (e.g., medical appointments and post discharge tests/labs). Plan for the follow-up of results from tests or labs that are pending at discharge. Identify the correct medicines and a plan for the patient to obtain them. Teach a written discharge plan the patient can understand. Educate the patient about his or her diagnosis and medicines. Review with the patient what to do if a problem arises. Assess the degree of the patient's understanding of the discharge plan and provide a telephone reinforcement of the discharge plan

Discharge planning program; Standard Care

Eligibility Criteria

• Age: 21 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Adult patient aged 21 years or older
• Underwent first time isolated elective CABG surgery for single, double, or triple CAD.
• Patient speak and read Arabic to eliminate any barriers of communication during the process of discharge and telephone call
• Patient who has contact telephone number
• Doesn't have Aortic calcification, and /or previous stroke
• Welling to participate and Able to provide informed consent

You may not qualify if:

• Adult patient aged 21 years or older
• Underwent first time isolated elective CABG surgery for single, double, or triple CAD.
• Patient speak and read Arabic to eliminate any barriers of communication during the process of discharge and telephone call
• Patient who has contact telephone number
• Doesn't have Aortic calcification, and /or previous stroke
• Welling to participate and Able to provide informed consent

Sponsors & Collaborators

• University of Jordan: lead
• Jordanian Royal Medical Services: collaborator

Study Sites (1)

University of Jordan

Amman, 11942, Jordan

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Masking Details: Non pharmacological intervention with no blinding
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Model Details: 2 groups Post test only

Study Record Dates

• First Submitted: August 22, 2020
• First Posted: August 27, 2020
• Study Start: August 1, 2020
• Primary Completion: June 1, 2024
• Study Completion: June 1, 2024
• Last Updated: March 19, 2024

Record last verified: 2024-03

Data Sharing

• IPD Sharing: Will not share

Locations

JO (1)