RecruitingNot ApplicableNCT07052266

Trial of Combined Obstetric Carrier Screening and Hereditary Cancer Screening

Feasibility of Obstetric and Cancer Universal Screening


Sponsor

Weill Medical College of Cornell University

Enrollment

550 participants

Start Date

Sep 2, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The investigators hypothesize that pregnancy and preconception care may be a feasible and effective time to offer inherited cancer risk screening. This study will assess interest in cancer genetic testing among patients receiving routine prenatal or preconception/fertility care. The goal is to evaluate the acceptability of BRCA1/2 testing when offered alongside standard prenatal genetic screening. The study will also explore whether universal screening in this population could support early cancer prevention and be cost-effective, especially among underserved populations.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 55 Years

Inclusion Criteria5

  • Age 18 years - 55 years
  • Pregnant patients receiving obstetrical-related care or receiving preconception/fertility care at a WCM-affiliated enrollment site.
  • Patients who have elected to undergo OCS with the WCM-affiliated obstetrics provider
  • Patients with prior OCS but planned to repeat OCS are eligible
  • Patients can speak and read in English or Spanish

Exclusion Criteria3

  • Patients who have previously completed a multigene hereditary cancer syndrome panel
  • Patients who have a hematologic cancer or hematologic pre-cancer
  • Patients who have a history of an autologous bone marrow transplant

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

GENETICMyRisk Hereditary Cancer Test

Subjects that are planning to proceed with OCS and enrolled in the trial will be contacted by the genetics clinician (by telephone or in person, based on subject preference) to review the option for HCS in addition to OCS. The WCM genetics clinician will review the potential risks and benefits, possible findings, and implications of findings for HCS. The genetics clinician will follow WCM standards (outlined by the WCM Genetics and Personalized Cancer Prevention Program https://wcinyp.org/GPCP) for informed consent counseling on the potential risks/benefits of HCS. The counseling regarding OCS will have already been performed by the obstetrical team as part of the standard of care. The genetics clinician will review that OCS is being performed as part of the patient's standard of care prenatal visit and HCS is an additional component that is being performed as part of participation in this clinical trial.


Locations(5)

Reproductive Medicine

Brooklyn, New York, United States

NewYork-Presbyterian Weill Cornell Medicine

Brooklyn, New York, United States

Reproductive Medicine

New York, New York, United States

Weill Cornell Medicine

New York, New York, United States

NewYork-Presbyterian Weill Cornell Medicine Queens

Queens, New York, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07052266


Related Trials