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Clinical Trials/NCT02568930
NCT02568930
Completed
Not Applicable

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

Northwestern University13 sites in 1 country694 target enrollmentOctober 15, 2015
ConditionsHeart Failure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure
Sponsor
Northwestern University
Enrollment
694
Locations
13
Primary Endpoint
Non-inferior change in patient HRQOL
Status
Completed
Last Updated
4 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
October 15, 2015
End Date
March 31, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kathleen Grady

Professor, Feinberg School of Medicine

Northwestern University

Eligibility Criteria

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

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Non-inferior change in patient HRQOL

Time Frame: baseline through 2 years after surgery

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 outcome) and HRQOL domains (physical, mental, and social \[secondary outcomes\]) from baseline through 2 years after surgery.

Secondary Outcomes

  • Non-inferior change in caregiver HRQOL(baseline through 2 years after surgery)
  • Risk factors related to poorer patient overall HRQOL(2 years after surgery)
  • Risk factors related to poorer caregiver overall HRQOL(2 years after surgery)
  • Distribution of QALYs(2 years after surgery)
  • Non-inferior rates of freedom from adverse events & symptoms(1 and 2 years after surgery)

Study Sites (13)

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