Heart Failure Clinical Trial

SUSTAIN-IT: Sustaining Quality of Life of the Aged: Heart Transplant or Mechanical Support?

Summary

The purpose of this study is to compare health-related quality of life (HRQOL) outcomes in older (60-80 years) advanced heart failure (HF) patients who undergo heart transplantation (HT) or mechanical circulatory support (MCS) as a permanent implant (i.e., destination therapy [DT]) and their caregivers. Our study will contribute to better patient-centered care of older advanced HF patients and their caregivers, by informing decision making and guiding strategies to enhance post-operative HRQOL.

View Full Description

Full Description

The purpose of this study is to compare health-related quality of life (HRQOL) outcomes in older (60-80 years) advanced heart failure (HF) patients who undergo heart transplantation (HT) or mechanical circulatory support (MCS) as a permanent implant (i.e., destination therapy [DT]) and their caregivers, risk factors for poor HRQOL, adverse event and symptom burden, and quality-adjusted life years (QALYs). Advanced HF patients, 60-80 years of age, are an appropriate target group for this study because they are receiving HTs and MCS devices more frequently, and despite a greater risk for poor clinical outcomes, they have acceptable rates of survival. Using a prospective, longitudinal design, our multi-site comparative effectiveness research will compare HRQOL outcomes in patients who receive HT or DT MCS and their caregivers, from baseline to 2 years post-operatively. The primary aim of this proposed study is to determine whether older advanced HF patients who undergo DT MCS, as compared to patients who undergo HT, experience non-inferior change in overall HRQOL (primary), and domains of HRQOL (physical, mental, and social) from baseline through 2 years after surgery. Secondary Aims are (1.) to determine whether caregivers of older advanced HF patients who undergo DT MCS, compared to caregivers of older advanced HF patients who undergo HT, experience non-inferior change in overall HRQOL and domains from baseline through 2 years after surgery; (2.-3.) to identify risk factors related to poorer overall HRQOL in older DT MCS patients and their caregivers, as compared to older HT patients and their caregivers, at 2 years after surgery; (4.) to determine whether older advanced HF patients who undergo DT MCS, as compared to patients who undergo HT, have non-inferior rates of freedom from adverse events & symptoms at 1 and 2 years after surgery; and (5) to evaluate the distribution of QALYs in older advanced HF patients who undergo DT MCS, as compared to patients who undergo HT at 2 years after surgery. Our proposed study will contribute to better patient-centered care of older advanced HF patients and their caregivers, by informing decision making and guiding strategies to enhance post-operative HRQOL.

View Eligibility Criteria

Eligibility Criteria

Patient Inclusion Criteria:

Advanced HF and listed with the United Network for Organ Sharing (UNOS) for a "primary" HT or scheduled to receive a "primary" DT LVAD;
Ages 60-80 years and able to speak, read, and understand English;
Willing to participate and ability to provide informed consent.

Caregiver Inclusion criteria:

Primary caregiver, identified by the patient, prior to DT MCS or while a candidate for HT;
Unpaid family member or friend who helps the patient with self-care;
Age > 21 years and able to speak, read, and write English;
Willing to participate and ability to provide informed consent.

Patient Exclusion criteria

Patient has a prior HT or MCS device
Patient is listed for multiple organ transplantation (i.e., heart/lung, heart/kidney, etc.)

Caregiver Exclusion criterion:

1) Patient refusal to participate.

Study is for people with:

Heart Failure

Estimated Enrollment:

694

Study ID:

NCT02568930

Recruitment Status:

Completed

Sponsor:

Northwestern University

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 13 Locations for this study

See Locations Near You

University of Alabama at Birmingham (UAB)
Birmingham Alabama, 35294, United States
Florida Hospital
Orlando Florida, 32803, United States
Northwestern University
Chicago Illinois, 60611, United States
Advocate Christ Medical Center
Oak Lawn Illinois, 60453, United States
University of Michigan
Ann Arbor Michigan, 48109, United States
University of Minnesota Medical Center-Fairview Health Services
Minneapolis Minnesota, 55454, United States
Saint Luke's Hospital
Kansas City Missouri, 64111, United States
Washington University
Saint Louis Missouri, 63110, United States
Columbia University
New York New York, 10032, United States
Cleveland Clinic
Cleveland Ohio, 44195, United States
The Ohio State University (OSU)
Columbus Ohio, 43210, United States
University of Pittsburgh Medical Center (UPMC)
Pittsburgh Pennsylvania, 15213, United States
University of Wisconsin-Madison
Madison Wisconsin, 53706, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

694

Study ID:

NCT02568930

Recruitment Status:

Completed

Sponsor:


Northwestern University

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider