Applying Population Management Best Practices to Preventative Genomic Medicine Trial
Enrolling by invitation · Not applicable
Conditions studied: Neoplastic Syndromes, Hereditary
In brief
Preventive genomic medicine, particularly identification of individuals with inherited cancer risk, can improve longevity and quality of life, yet adherence to risk management following cancer genomic testing is poor. The proposed research refines and evaluates two highly scalable population management interventions, web resources and personalized outreach, designed to improve access and use of recommended risk management following cancer genetic testing. Research activities will be conducted in a vertically integrated health system and federally qualified health center and will address post-testing quality and patient safety concerns that are minimizing patient benefit and slowing investments in real world genomic medicine implementation.
Key facts
- Study ID
- NCT07053813
- Run by
- University of Washington
- People needed
- 900
- Starts
- 2025-07-01
- Expected to finish
- 2028-07-01
- Last updated by the study team
- 2026-02-27
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Clinically actionable variant in at least one high penetrance cancer-related gene
- Age- and sex- eligible for guideline indicated risk management
- Remains eligible for risk management, given personal cancer and surgical history
You may not qualify if…
- Previously opted out of research
- Previously opted out of genetic research
- On hospice or palliative care
- Has advanced dementia or severe cognitive impairment
Where it is running
- Denver Health — Denver, Colorado, United States
- Kaiser Northwest — Portland, Oregon, United States
Full record on ClinicalTrials.gov
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