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NCT06081517Recruiting

Evaluating Disparities in Precision Oncology

Indiana University

Start Date

1/26/2024

Completion Date

12/1/2028

Summary

This is a non-randomized observational trial designed to collect detailed clinical, social determinant, and genomic data from patients enrolled in molecular oncology tumor boards across four comprehensive cancer centers.

Detailed Description

This study proposes an innovative approach leveraging the molecular tumor boards across four comprehensive cancer centers, where real- world, diverse patients with metastatic cancer are seen receiving a broad scope of therapies in the context of precision medicine. The study plans to collect detailed clinical, social, and genomic data from patients to identify significant contributors of disparate survival and toxicity outcomes for patients with metastatic cancer.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: 1. Ability to provide written informed consent and HIPAA authorization 2. Patients must be ≥ 18 years old at the time of consent 3. Patients who have or are planning to undergo molecular testing as part of their routine cancer care Exclusion Criteria: N/A

Interventions

BEHAVIORAL

Social Determinants of Health and toxicity questionnaires

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Conditions

Metastatic CancerAdvanced Cancer

Locations

Indiana University Health Melvin and Bren Simon Comprehensive Cancer Center

Indianapolis, Indiana 46202

United States