New online tool could help doctors spot hidden cancer risks
NCT ID NCT05079334
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a web-based tool called MeTree that collects family health history to estimate a person's risk for inherited cancer. Over 1,800 adults from three medical centers participated. The goal was to see if the tool helps identify high-risk patients more efficiently than standard clinic methods, and to offer genetic counseling to those who need it.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- MeTree family health history questionnaire
- What this could lead to
- If successful, this tool could help doctors more easily spot patients who might have inherited cancer risks, leading to earlier genetic counseling and better prevention.
- What could go wrong
- This study is about testing a process, not a treatment. It may not show big improvements in health outcomes, and results might not apply to all clinics or populations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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1,847 people
The number who actually took part.
- Started
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Jan 2022
- Finished
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Sep 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Anyone over 18 years old, receiving care at our study site (virtual included), and willing/able to use the internet.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Receiving care at sites included in study * Able to read and communicate in English * Willing to use the Internet * Currently enrolled in the patient portal, or willing to enroll (VUMC-specific) Exclusion Criteria: * Non-study site patient * Diagnosed with a terminal illness * Unable to speak/read English * Unable/unwilling to use the Internet * Previous genetic testing and/or counseling from the VUMC Hereditary Cancer Clinic
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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
Locations
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Meharry Medical College
Nashville, Tennessee, 37208, United States
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Vanderbilt University Medical Center
Nashville, Tennessee, 37212, United States
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Other studies related to the condition(s) this trial covers.