Can online genetic counseling boost cancer testing rates?
NCT ID NCT03985852
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study looked at over 3,000 people at risk for certain cancers to see if a patient-directed online genetic counseling approach works as well as standard care. Participants were randomly assigned to either use an automated genetics education assistant or receive enhanced standard counseling. The goal was to compare how many people completed genetic testing and followed cancer prevention recommendations.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could show that a patient-directed online genetic counseling model is as effective as standard care, making genetic testing more accessible.
- What could go wrong
- This is an observational study comparing service delivery models, not testing a new treatment. Results may not apply to all populations or settings.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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3,073 people
The number who actually took part.
- Started
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Feb 2020
- Finished
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Aug 2024
- 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.
- Ages
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25 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Speaks English or Spanish AND * First degree relative or second degree relative diagnosed with the following regardless of age: Ovarian Cancer, Pancreas Cancer OR * First degree relative or second degree relative diagnosed with the following \<50 years of age: Breast Cancer, Colorectal Cancer, Endometrial Cancer. OR * Three of more relatives on the same side of the family diagnosed with the following clusters of cancer regardless of age: * Breast Cancer, Ovarian Cancer, Pancreas Cancer, Prostate Cancer * Colorectal Cancer, Endometrial Cancer, Ovarian Cancer, Pancreas Cancer, Urinary tract, Brain, Small intestine * Melanoma, Pancreas Cancer OR * Ashkenazi Jewish ancestry and family history of Breast Cancer, Ovarian Cancer, Pancreas Cancer, Prostate Cancer. Exclusion Criteria: * Patients with a prior cancer diagnosis, other than non-melanoma skin cancer, and/or prior genetic counseling or testing related to hereditary cancer. * Patients unable to access the patient portal
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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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NYU School of Medicine
New York, New York, 10016, United States
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University of Utah
Salt Lake City, Utah, 84112, United States
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