Actively Recruiting
Targeted Navigation in Hepatocellular Carcinoma (HCC)
Led by University of Miami · Updated on 2025-07-15
100
Participants Needed
1
Research Sites
132 weeks
Total Duration
On this page
Sponsors
U
University of Miami
Lead Sponsor
T
The V Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
The investigators are trying to learn more about the personal perceptions and experiences regarding the needs of patients with liver cancer to help improve the care of all patients. The investigators would like to know whether there are needs that patients have or are aware of, especially those needs that the investigators have not been able to address. The investigators aim to develop a program that helps participants and participant's families to navigate the process of being diagnosed with liver cancer and receiving treatment.
CONDITIONS
Official Title
Targeted Navigation in Hepatocellular Carcinoma (HCC)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults age 18 or older
- Diagnosis of hepatocellular carcinoma confirmed by clinical chart review and ICD-10 C22.0
- Enrolled or eligible for enrollment in the Unified Prospective Registry and Biorepository of Patients with Chronic Liver Disease or Hepatobiliary Cancers including HCC and Cholangiocarcinoma
- Able to provide informed consent
- Advocates self-identifying as having had hepatocellular carcinoma
- Caregivers or support persons of an HCC patient
- Physicians, social workers, nurse navigators, or research coordinators involved in HCC patient care who self-identify as such
You will not qualify if you...
- Unable to speak English or Spanish
- West Haven Grade 2 or higher hepatic encephalopathy or other cognitive impairment
- Unable or unwilling to provide informed consent
- Individuals under 18 years old (infants, children, teenagers)
- Prisoners
- Pregnant women are not excluded, but no pregnancy or fetal data will be collected
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Miami
Miami, Florida, United States, 33136
Actively Recruiting
Research Team
G
Gloria Figueroa
CONTACT
P
Patricia Jones, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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