Recruiting NCT06053333

Social Determinants of Health in Hepatobiliary Cancer Patients

— Observational Malignant Hepatobiliary Neoplasm

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: Malignant Hepatobiliary Neoplasm. 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 →

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Overview

This study evaluates barriers to receiving care and risks associated with developing cancer among patients diagnosed with hepatobiliary cancer.

Detailed description

PRIMARY OBJECTIVE:

I. To characterize the social determinants of health - and specifically travel-limiting access to cancer care but also other issues, such as trouble in finding childcare, joblessness, and limited education - among SEA Americans with hepatobiliary cancers, exposure risk including aflatoxin and viral hepatitis among other exposures.

OUTLINE: This is an observational study.

Patients complete a questionnaire, undergo blood, urine, and buccal swab sample collection and have their medical records reviewed on study. Patients also undergo collection of clinically archived tissue samples on study.

Interventions

Other Non-Interventional Study
Non-interventional study

Primary outcome measures

Percentage of patients reporting transportation barriers that affect medical care [Time frame: Baseline; up to 2 years]

Eligibility criteria

Inclusion criteria

Patients 18+ year of age with hepatobiliary cancers

Exclusion criteria

Patients under 18 years of age

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

Mayo Clinic in Rochester — Rochester

Identifiers

NCT: NCT06053333 · 22-012368 · NCI-2023-05784 · 22-012368 · K23MD017217

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗