Trial of Combined Obstetric Carrier Screening and Hereditary Cancer Screening (NCT07052266)
Feasibility of Obstetric and Cancer Universal Screening
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Reproductive Medicine — Brooklyn, New York
Age range: 18 Years to 55 Years
🧪 Interventions in This Study
- MyRisk Hereditary Cancer Test (GENETIC)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (5 Sites)
- Reproductive Medicine — Brooklyn, New York
- NewYork-Presbyterian Weill Cornell Medicine — Brooklyn, New York
- Reproductive Medicine — New York, New York
- Weill Cornell Medicine — New York, New York
- NewYork-Presbyterian Weill Cornell Medicine Queens — Queens, New York
📞 Contact the Study Coordinator
Phone: (914) 312-7488
Email: stl4013@med.cornell.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Hereditary Cancer Syndromes
- Closing the GAPS: Guideline Adherence, Prevention and Surveillance in Hereditary Cancer — Boston, Massachusetts
Explore by condition: All Hereditary Cancer Syndromes clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.