Web tool aims to empower rare cancer patients in genomic choices
NCT ID NCT06910670
First seen Jul 21, 2026 · Last updated Jul 24, 2026 · Updated 3 times
Summary
This study tests an expanded web-based decision aid for people with cholangiocarcinoma, colorectal cancer, or multiple myeloma. Participants use the tool to choose which genomic results—such as cancer biomarkers or inherited risks—they want to receive. The goal is to see if the tool improves confidence and reduces conflict in making these complex decisions.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- a web-based decision aid tool
- What this could lead to
- If successful, this tool could help patients with rare cancers make more informed choices about receiving genomic test results, potentially improving their confidence and reducing regret.
- What could go wrong
- This is a small, early-stage trial focused on decision-making, not treatment. The tool may not significantly improve outcomes or may not work well for all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Washington University School of Medicine
RECRUITINGSt Louis, Missouri, 63110, United States
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
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