Clinical trial Recruiting at 2 sites Interventional Ages 18 to 25

Health Advocate program for young liver transplant recipients

Official title: HEalth Advocate for Liver Transplantation: Improving Transition of Care for Adolescent Liver Transplant Recipients

Run by University of California, San Francisco · NCT06386198 · Data updated 2026-11-12

This study is testing a new program that adds a Health Advocate to help young adults who had a liver transplant manage their care and connect with resources as they transition to adult healthcare.

Quick facts

Study typeInterventional
Ages18 Years to 25 Years
SexAll
Enrollment20 (estimated)
SponsorUniversity of California, San Francisco
Academic / other
Locations2 sites (San Francisco, California and 1 other locations)
StatusRecruiting
StartedMarch 3, 2024
Main results expectedJune 30, 2029
Study endsJune 30, 2030
Registry record updatedAugust 11, 2026
Trial IDNCT06386198 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adolescents aged 18-25 who have received a liver transplant more than one year ago and face unmet social risks.

Probably not a fit

Patients with significant cognitive impairment or those who do not meet the age criteria will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The HEAL-Tx Transition of Care Pilot is an intervention designed to integrate a Health Advocate into the transplant team to assist adolescents transitioning to adult liver transplant care. This pilot program aims to assess the feasibility and acceptability of the Health Advocate's role, which includes coordinating medical care, providing financial assistance, and connecting patients with community resources. By focusing on adolescents aged 18-25 who have received a liver transplant over a year ago, the study seeks to improve self-management and communication between patients and healthcare providers. The effectiveness of this intervention will be measured using the RE-AIM framework.

Why it matters

Potential benefit: If successful, this program could enhance the transition process for young liver transplant recipients, leading to better health outcomes and improved quality of life.

How similar studies have gone: Other studies have shown success with similar health advocate approaches in improving patient outcomes, indicating potential for this intervention.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Patient has received a liver transplant \>1 year ago
2. Study team has screened patient and discussed with the primary transplant practitioner that patient may benefit from the Health Advocate program.
3. Patient has an unmet social risk (e.g., food insecurity) or MLVI \>/= 2.0.
4. Patient will be transferred to adult transplant team in \<6 months.
5. Patient can read and write English or Spanish
6. Patient is between 18-25 years old and can provide informed consent.
7. Patient has a working phone and smart device capable of video and/or audio virtual visits via Zoom.

Exclusion Criteria:

* Patient has significant cognitive impairment.
* Does not meet age criteria
* Patient is a ward of the state.
* Non-English, non-Spanish speakers.
* Non-US residents.

Where it's running

  • University of California San Francisco
    San Francisco, California, United States
    Recruiting
  • Children's Healthcare of Atlanta
    Atlanta, Georgia, United States
    Recruiting

Study contacts

  • Principal investigator: Sharad Wadhwani, MD, MPH — University of California, San Francisco
  • Study coordinator: Sharad Wadhwani, MD, MPH
  • Email: sharad.wadhwani@ucsf.edu
  • Phone: 510-428-3058

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.