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Achieving Equity in Genomic Testing for Breast Cancer Through Partner-Led Strategies and Policies

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Stanford University

Status

Active, not recruiting

Conditions

Breast Cancer

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to identify the barriers, and the extent of said barriers, to genomic testing for breast cancer patients among low-income and minority populations, particularly throughout Northern California. The investigators have created a survey that is available online for any patient with cancer to fill out voluntarily regarding their experiences to date. The survey is available at: https://stanforduniversity.qualtrics.com/jfe/form/SV_7VElf8oesWcB3bE

Full description

The study has two main data-collecting phases. In phase 1, the investigators will engage multilevel stakeholders to respond to a survey assessing experience with and perceptions of genomic testing and its accessibility for patients with breast cancer in California. In phase 2, selected and interested survey participants who voluntarily provide their contact information on the survey will be asked to participate in an in-depth 1:1 semi-structured interview to explore disparities in genomic testing for breast cancer more closely. The investigators will then utilize their findings from both phases to present aggregate findings to an Expert Panel and Community Advisory Board and work together to develop policy recommendations. The policy recommendations will then be presented to policy makers, with the aim of identifying sustainable solutions that address breast cancer treatment and outcome disparities throughout Northern California.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patients must be 18 years or older.
  • Patients who opt in to complete the survey.
  • Patients must have the capacity to verbally consent for the interview.

Exclusion criteria

  • Patients who under the age of 18 years old.

Trial design

150 participants in 1 patient group

Patients and Caregivers
Description:
We will survey 100 patients and 50 caregivers.

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Emily H Wood; Manali A Patel

Data sourced from clinicaltrials.gov

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