Purpose

The HEAL-Tx is a 90-day intervention, in which a Health Advocate works with eligible families to identify and apply for community-based resources, alert healthcare providers to challenges the family is encountering, and guide health system navigation (e.g., coordinating appointments). Families in the control arm will receive a printed handout that provides contact information for local community-based resources. Families in the treatment arm will receive HEAL-Tx.

Condition

Eligibility

Eligible Ages
Between 0 Years and 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patient <18 years old at the time of liver transplant - Received a liver transplant within past 90 days - Family endorses material economic hardship on 10-questions Accountable Healthcare Communities screening tool. - Will receive follow-up care for at least 2 years - Family can read or write English or Spanish - A Legally Authorized Representative (LAR) can provide consent, and for children (12-17 years of age, the child is willing/able to provide assent.) - Family has a working phone and smartphone device capable of receiving calls or virtual visits via Zoom.

Exclusion Criteria

  • Patient has severe cognitive impairment. - 18 years of age or older at the time of consent - Patient unwilling or unable to consent/participate - Patient is a ward of the state (e.g. foster care) since present circumstances may not be reflective of child's past or future circumstances. - Non-English, non-Spanish speakers as ICFs, HIPAA authorization form, surveys, and interviews will only be available in these 2 languages. Languages besides English and Spanish are excluded from this study.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Health Services Research
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Health Advocate Intervention
The caregiver will receive 90-days of tailored health advocate intervention
  • Behavioral: Health advocate
    The health advocate is a trained individual who is not a part of the medical team. They work directly with the caregivers of patients who have received a liver transplantation to assist them with navigating the healthcare system, find resources, and relay any concerns to their medical team. They work with an assigned family for 90-days and tailor their intervention to meet the families social needs.
    Other names:
    • HA
Active Comparator
Enhanced Control
The caregiver will receive a printed sheet of resources once and a follow-up call at the 45-day timepoint with a reminder of the suggested resources.
  • Behavioral: Enhanced Control
    Caregivers in the control arm will receive enhanced standard of care: they will be given a handout with a list of resources specific to their hardship and their home ZIP code. They will receive a follow-up call at 45 days with a reminder of the suggested resources.

Recruiting Locations

University of California, San Francisco
San Francisco, California 94158

University of Pittsburgh Medical Center | Children Hospital of Pittsburgh
Pittsburgh, Pennsylvania 15224
Contact:
Susan M Richey, RN
412-692-6337
richeys@upmc.edu

More Details

Status
Recruiting
Sponsor
University of California, San Francisco

Study Contact

Bethany Reyna, BA, CCRP
415-476-7748
Bethany.reyna@ucsf.edu

Detailed Description

HEAL-Tx trial is a Type 1 hybrid effectiveness-implementation trial across 6 U.S. transplant centers (UCSF, Seattle Children's Hospital, Stanford University, Children's Healthcare of Atlanta, University of Pittsburgh, Children's Hospital of Colorado.) Children/families will be screened for material economic hardship as part of standard of care during their transplant hospitalization using the 10-question Accountable Healthcare Communities tool. Families who report material economic hardship will be approached for study participation, and those who consent will be randomized to either the control or treatment arm. Participants in the control arm will receive enhanced standard of care: they will receive a printed handout with a list of resources specific to their hardship and their home ZIP code. They will also receive a follow-up call at 45-days with a reminder of the suggested resources. Participants in the treatment arm will receive a customized 90-day Health Advocate intervention. Both the treatment and control arm group will complete a baseline interview and a close-out 90-day interview to assess outcomes and experiences with the intervention. The treatment arm will have one additional interview at the 45-day timepoint. Once both arms complete treatment, they will have data extracted from their medical records at the 1, and 2-year timepoint.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.