Status:

RECRUITING

Tumor Genomic Pre-test Counseling Tool for Black or African-American Men With Prostate Cancer

Lead Sponsor:

University of California, San Francisco

Collaborating Sponsors:

Prostate Cancer Foundation

Conditions:

Prostate Cancer

Prostate Cancer Metastatic

Eligibility:

MALE

18+ years

Phase:

NA

Brief Summary

The overall goal of the study is to improve equitable delivery of pre-Tumor genetic testing (TGT) counseling tool for Black or African American men with metastatic prostate cancer and evaluating the t...

Detailed Description

PRIMARY OBJECTIVES: Stage 1: To evaluate education quality of the intervention in Black or African American men with prostate cancer. Stage 2: To evaluate feasibility of the TGT intervention among B...

Eligibility Criteria

Inclusion

  • Stage 1:
  • Age 18-years-old or older
  • Identifies as Black or African American, by either chart documentation or participant self-report. Mixed-race including Black or African American is included.
  • Metastatic prostate cancer, by either chart documentation or participant self-report. Pathology report not needed.
  • Able to understand study procedures and to comply with them for the entire length of the study.
  • Able to understand a written information sheet and willing to verbally consent.
  • Fluent in English (reading, writing, and speaking)
  • Stage 2:
  • Age 18-years-old or older
  • Identifies as Black or African-American, by either chart documentation or participant self-report. Mixed-race including Black or African-American is included.
  • Metastatic prostate cancer, by either chart documentation or participant self-report. Pathology report not needed.
  • Able to understand study procedures and to comply with them for the entire length of the study.
  • Fluent in English (reading, writing, and speaking).
  • Anticipated discussion of TGT within 0-90 days of enrollment, per treating oncology provider's discretion. TGT involves use of any cancer genetic sequencing (whether standard-of-care or part of a research protocol) via any one of the following:
  • Somatic DNA testing of already-collected tissue.
  • Somatic DNA testing of tissue to be collected in the future via biopsy, surgery, or other procedure.
  • Blood-based DNA testing to evaluate for circulating tumor DNA.
  • Able to understand a written informed consent document and willing to sign it.

Exclusion

  • Contraindication to any study-related procedure or assessment in either stage.

Key Trial Info

Start Date :

December 1 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

August 31 2027

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT06171139

Start Date

December 1 2023

End Date

August 31 2027

Last Update

July 23 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

University of California

San Francisco, California, United States, 94143