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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06386198
Other study ID # 23-40699
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 3, 2024
Est. completion date June 30, 2026

Study information

Verified date April 2024
Source University of California, San Francisco
Contact Sharad Wadhwani, MD, MPH
Phone 510-428-3058
Email sharad.wadhwani@ucsf.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Health Advocate for Liver Transplant (HEAL-Tx) Transition of Care Pilot is a nonrandomized, open-label intervention pilot of a health advocate intervention aimed to assess feasibility and acceptability of integrating a Health Advocate onto the transplant team to help adolescents transition their care to adult transplant teams. Across studies, health advocate roles vary, and can include coordinating medical care treatment, facilitating financial assistance (e.g., taxi vouchers), and connecting patients to community resources, which can improve self-management, mitigate social risks, and lead to better communication between the healthcare system and the family. In this pilot, the investigators will adapt this intervention for adolescent/young adult liver transplant patients and measure acceptability and feasibility according to RE-AIM.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date June 30, 2026
Est. primary completion date June 30, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 25 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Health Advocate
The Health Advocate intervention will include helping pediatric liver transplant recipients and their families address unmet household social needs (e.g., food insecurity), improve patient-provider communication, and enhance care coordination.

Locations

Country Name City State
United States Children's Healthcare of Atlanta Atlanta Georgia
United States University of California San Francisco San Francisco California

Sponsors (2)

Lead Sponsor Collaborator
University of California, San Francisco American Society of Transplantation

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in patient experience The investigators will administer a survey of patient experience at study enrollment and at the end of the intervention to assess for changes in patient experience with the transplant team. These questions will focus on experiences receiving transplant care, experiences discussing social needs with the transplant team, and overall subjective assessment of the transplant recipient's overall health. Baseline and 180 days
Secondary Change in medication adherence using MLVI Medication level variability index (MLVI) defined as the standard deviation of at least 3 outpatient tacrolimus trough levels (binary >/=2.0 or <2.0). The investigators will assess this at study entry and again at 180 days. Baseline and 180 days
Secondary The quality of health advocate interactions with the participants, healthcare team, and community-based resources. The Health Advocate will keep a detailed journal entry after each encounter and certain Health Advocate interactions will be recorded. The investigators will qualitatively analyze these journal entries and recordings to identify what functions the health advocate undertook. 180 days
Secondary A qualitative assessment of patient and healthcare provider satisfaction with the Health Advocate intervention. The investigators will conduct in-depth interviews with the patient participant and clinical team members to assess overall satisfaction with the intervention. 180 days
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