Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:01 AM
Ignite Modification Date:
2025-12-25 @ 4:01 AM
NCT ID:
NCT03470402
Eligibility Criteria:
Inclusion Criteria (Patient Participants):
* Women, age 21-75 years
* Meets criteria for genetic testing based on family history
* Sees a primary care provider in the Columbia University (CUMC) /New York Presbyterian (NYP) Ambulatory Care Network
* Understands as is willing to provide informed consent in English or in Spanish
Exclusion Criteria (Patient Participants):
* Prior genetic counseling or testing for hereditary breast and ovarian cancer (HBOC)
* A personal history of breast or ovarian cancer
Inclusion Criteria (Health Care Provider Participants):
* Primary care providers, such as attending physicians, residents, nurse practitioners, physician assistants, and midwives, who see patients at CUMC/NYP Ambulatory Care Network clinics
* Able to provide informed consent
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
21 Years
Maximum Age:
75 Years
Study:
NCT03470402
Study Brief:
Protocol Section:
NCT03470402