Using artificial intelligence to improve breast cancer screening in Norway

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial aims to compare breast cancer detection rates among women whose mammograms are interpreted using artificial intelligence (AI) alongside one or two radiologists versus those interpreted through standard double reading. The study addresses the challenges of missed cancers in traditional screening methods and the shortage of breast radiologists. Participants will be randomly assigned to either the AI-assisted interpretation group or the control group, with all examinations analyzed by AI to determine the risk of malignancy. The goal is to demonstrate that AI-assisted interpretation is at least as effective as the standard procedure.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Women attending the population-based mammography screening program BreastScreen Norway providing a signed, informed consent

Exclusion Criteria:

* Women attending the population-based mammography screening program BreastScreen Norway not providing a signed, informed consent

Where it's running

• Cancer Registry of Norway, Norwegian Institute of Public Health
  Oslo, Norway Recruiting

Study contacts

• Principal investigator: Solveig Hofvind, PhD — Norwegian Institute of Public Health
• Study coordinator: Solveig Hofvind, PhD
• Email: sshh@kreftregisteret.no
• Phone: 22928828

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.