Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06068491

Veteran-Centered Care for Advanced Liver Disease (Vet-CALD)

Led by VA Office of Research and Development · Updated on 2026-02-06

450

Participants Needed

8

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Advanced liver disease is a serious illness that disproportionately affects Veterans, many of whom hope for curative liver transplantation. However, too few receive a transplant and most continue to suffer from increasing symptoms and hospitalizations. The proposed project uses a whole person, Veteran-centered approach that identifies Veterans with advanced liver disease using a population-based health management system and integrates curative and early supportive care using a telemedicine-based nurse care counselor to (1) discuss patient's understanding of illness severity and prognosis, (2) identify priorities and care preferences and (3) align curative and supportive care options to achieve patient priorities. Study outcomes include changes in (1) rates of consideration for liver transplantation, and (2) completion of serious illness discussions. Findings will inform adaptations to the intervention and facilitators for its dissemination.

CONDITIONS

Official Title

Veteran-Centered Care for Advanced Liver Disease (Vet-CALD)

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients will be between 18 and 80 years of age
  • Patients must be Veterans
  • Patients must have been in care at one of the recruiting sites with 1 or more encounters in primary care or GI/Hepatology in the last 24 months
  • Patients must have advanced liver disease, defined by ICD-10 codes for cirrhosis complications (ever) or MELD 3.0 >12 or MELD-Na >12 or Fibroscan LSM >20kpa
Not Eligible

You will not qualify if you...

  • Non-Veteran patients
  • Patients who do not speak English, do not have access to a telephone or computers, or who are unable to complete a valid informed consent form after three attempts
  • Patients who have already made significant progress toward study endpoints: prior liver transplantation, being on the transplant waiting list, or formal liver transplant evaluation in the past 3 years
  • Patients with very limited life expectancy such as advanced cancer, acute-on-chronic liver failure, or hospice patients
  • Patients hospitalized, or in long term care facilities or nursing homes at the time they meet inclusion criteria
  • Patients with uncontrolled mental health conditions or schizophrenia documented in their medical chart

AI-Screening

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Trial Site Locations

Total: 8 locations

1

Central Arkansas Veterans Healthcare System , Little Rock, AR

Little Rock, Arkansas, United States, 72205

Actively Recruiting

2

VA Long Beach Healthcare System, Long Beach, CA

Long Beach, California, United States, 90822

Not Yet Recruiting

3

VA Palo Alto Health Care System, Palo Alto, CA

Palo Alto, California, United States, 94304-1207

Actively Recruiting

4

VA Greater Los Angeles Healthcare System, West Los Angeles, CA

West Los Angeles, California, United States, 90073-1003

Actively Recruiting

5

VA Connecticut Healthcare System West Haven Campus, West Haven, CT

West Haven, Connecticut, United States, 06516-2770

Not Yet Recruiting

6

Miami VA Healthcare System, Miami, FL

Miami, Florida, United States, 33125

Not Yet Recruiting

7

VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX

Dallas, Texas, United States, 75216-7167

Not Yet Recruiting

8

Michael E. DeBakey VA Medical Center, Houston, TX

Houston, Texas, United States, 77030-4211

Actively Recruiting

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Research Team

J

Juana Campos, MA

CONTACT

F

Fasiha Kanwal, MD MSHS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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