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Recruiting NCT07312162

Multilevel Determinants of Socioeconomic Disparities in Geographic Late-Stage Hepatocellular Carcinoma Hotspots

Observational Hepatocellular Carcinoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Non-Interventional Study.
Who it may be relevant to
Registry conditions: Hepatocellular Carcinoma. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study evaluates barriers to early detection of liver cancer.

Detailed description

PRIMARY OBJECTIVES:

I. To identify individual-level social and clinical determinants of socioeconomic disparities in late stage Hepatocellular Carcinoma (HCC) burden with a prospective survey of patients with incident HCC. II. To qualitatively explore the multilevel barriers to completion of the early detection pathway for HCC in low socioeconomic status (SES) populations.

OUTLINE: This is an observational study.

Participants complete surveys, have their medical records reviewed, and may complete an interview on study.

Interventions

  • Other Non-Interventional Study
    Non-interventional study

Primary outcome measures

  • Social determinants of health [Time frame: Up to 4 years]
  • Barriers to completion of the early detection pathway for liver cancer [Time frame: Up to 4 years]

Eligibility criteria

Inclusion criteria

  • \* Adults (18+)
  • New diagnosis of HCC
  • Able to provide informed consent

Additional criteria:

  • Must complete survey
  • Residential address in a late stage hotspot
  • Medicaid insurance or uninsured
  • English, Spanish and Chinese speakers

Exclusion criteria

  • \* Residence outside of Los Angeles County
  • Non-HCC liver tumors
  • Incarcerated patients
  • Pregnant women

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • USC / Norris Comprehensive Cancer Center — Los Angeles

Identifiers

NCT: NCT07312162 · 19PS-21-7 · NCI-2024-03737 · 19PS-21-7 · K23MD016963 · P30CA014089

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗