AI and quick looks: could they speed up breast cancer screening?
NCT ID NCT05960188
First seen Jun 27, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This study tested whether radiologists can safely skip looking at detailed 3D breast scans when a quick 2D image or an AI score suggests the case is normal. Sixteen radiologists briefly viewed each case and rated how likely it was normal, then saw the AI's opinion. The goal is to see if this 'self-triage' could speed up screening without missing cancers. It's a very early step and not ready for real-world use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AI opinion (behavioral intervention)
- What this could lead to
- If successful, this could help radiologists work faster by safely skipping unnecessary 3D scans for clearly normal cases, potentially reducing screening time and cost.
- What could go wrong
- This is a very small, early study with only 16 radiologists. It does not test real-world outcomes, and the approach may not be safe or acceptable in practice.
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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16 people
The number who actually took part.
- Started
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Mar 2023
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- 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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18 years and older
- 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: * Must be Radiologists or radiology trainees * some experience reading mammography. Exclusion Criteria: * acuity less than 20/25 with correction
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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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Visual Attention Lab / Brigham and Women's Hospital
Boston, Massachusetts, 02215, United States
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Other studies related to the condition(s) this trial covers.
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