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Reducing Readmission Rates by Providing a Comprehensive Transition Plan From Hospital to Home for Cardiac Surgery Patients.

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Johns Hopkins University

Status

Completed

Conditions

Cardiac Surgery

Treatments

Behavioral: Home Visit

Study type

Interventional

Funder types

Other

Identifiers

NCT04373850
IRB00097613

Details and patient eligibility

About

Patients who undergo cardiac surgery will be screened by a team member with the risk score once the patient has been admitted to the Cardiovascular Progressive Care Unit (CVPCU) after surgery. Participants will be randomized to the intervention or the control group. Both groups will receive standard discharge planning. In addition, the intervention group will have a nurse practitioner (NP) who will be responsible to verify that each essential step of the discharge process has been completed and will visit the patient in patient's home after discharge to complete a physical, review medications, titrate medications as needed, prescribe any necessary treatments, and perform education. The primary outcome variable will be a decrease in the 30 day readmission rate comparing high risk patients at pre and post intervention.

Enrollment

450 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All patients 18 years of age or greater who have had cardiac surgery procedures including coronary artery bypass surgery (CABG), valve replacement, aortic aneurysm repair, and combined CABG and valve procedures.

Exclusion criteria

  • Patients who have undergone orthotopic heart transplantation, orthotopic lung transplantation, or orthotopic heart-lung transplantation
  • Patients who have undergone ventricular assist device placement
  • Patients who do not reside in Maryland
  • Non English speaking patients
  • Patients discharged to a facility.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

450 participants in 2 patient groups

Home visit group
Experimental group
Description:
Will receive a home visit after discharge in addition to the standard discharge planning.
Treatment:
Behavioral: Home Visit
Control group
No Intervention group
Description:
Will receive only the standard discharge planning.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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