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Clinical Trials/NCT03044535
NCT03044535
Completed
N/A

Mechanical Circulatory Support: Measures of Adjustment and Quality of Life

Northwestern University12 sites in 1 country895 target enrollmentOctober 26, 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Quality of Life
Sponsor
Northwestern University
Enrollment
895
Locations
12
Primary Endpoint
Creation of new MCS A-QOL item banks and short forms and validation of existing instruments
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to develop a measurement system to assess adjustment to mechanical circulatory support (MCS) (also referred to as a ventricular assist device [VAD]) and health-related quality of life (HRQOL) in patients with advanced heart failure who receive a VAD. This investigators refer to this measurement system as Mechanical Circulatory Support: Adjustment and Quality of Life (MCS A-QOL).

Detailed Description

It is estimated that 5.1 million U.S. adults have heart failure, with an incidence of 825,000 new cases annually. The prevalence of heart failure is expected to increase by 46% from 2012 to 2030. Mechanical circulatory support (MCS) has been developed as a bridge to heart transplantation and as permanent support (i.e., destination therapy). MCS devices help the heart pump blood to the body. Left ventricular assist devices (LVADs), a type of MCS, support the left heart. Health-related quality of life (HRQOL) is a very important outcome that advanced heart failure patients care about when making health care decisions, including when considering surgical treatment options, such as heart transplantation and mechanical circulatory support. Currently available HRQOL questionnaires do not assess the unique burdens of MCS, such as changing power sources and driveline exit site dressings; safety precautions (e.g., no immersion in water, need for an MCS-trained caregiver); troubleshooting VAD alarms; and MCS-specific complications, often associated with frequent hospitalizations. Since these questionnaires do not focus on issues of concern to MCS patients, they lack sensitivity and precision to measure the potentially wide-ranging impact of MCS on HRQOL. Guided by the investigators empirically supported MCS A-QOL conceptual model, the investigators will use state-of-the-science psychometric measurement methods to create "item banks" (sets of items that comprise carefully calibrated questions which define and quantify a common theme) from the investigators existing MCS A-QOL item pools (library of relevant items). Using calibrated item banks, the investigators will develop computer adaptive tests (CATs) and fixed-length short forms to reduce respondent burden and enhance measurement precision. The investigators will assess reliability, validity, responsiveness to change, and clinically important differences of MCS A-QOL measures.

Registry
clinicaltrials.gov
Start Date
October 26, 2016
End Date
February 28, 2020
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kathleen Grady

Professor of Surgery and Medicine, Feinberg School of Medicine at Northwestern University

Northwestern University

Eligibility Criteria

Inclusion Criteria

  • Patient with a continuous flow MCS device left (L)VAD who is more than 3 months post-implant at the following intervals: 3, 6, 12, 18, 24, 30, 36, 42, 48 months and every 6 months thereafter. Note: patients can have had prior MCS devices.
  • The continuous flow MCS device, implant strategy can be a bridge to transplant, destination therapy, or bridge to recovery
  • Age \>= 19 years and able to speak and understand English
  • Sufficient cognitive ability to provide self-report data on a computer touchscreen/standard computer and/or on paper-based forms with minimal assistance
  • Willing to participate and able to give written informed consent

Exclusion Criteria

  • Has a bi-VAD, right (R)VAD, or total artificial heart

Outcomes

Primary Outcomes

Creation of new MCS A-QOL item banks and short forms and validation of existing instruments

Time Frame: Longitudinally: baseline through 6 months post-MCS implant and cross-sectionally through 10 years post-MCS implant

Psychometric measurement methods will be used to create new "item banks" (sets of items that comprise carefully calibrated questions which define and quantify a common theme) and short forms from our existing MCS A-QOL item pools (library of relevant items). Psychometric properties (e.g., reliability, validity, etc) of these new measures and existing instruments, some of them modified, will be evaluated, in order to provide evidence of their clinical utility for measuring adjustment to MCS and HRQOL.

Study Sites (12)

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