Screening vs. symptoms: which breast cancer detection leads to better life after treatment?
NCT ID NCT03877029
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study looked at over 4,400 women to compare long-term quality of life between those whose breast cancer was found through screening and those whose cancer was found through symptoms. Researchers measured quality of life at different times after diagnosis and also compared results to women who had screening but never had breast cancer. The goal is to understand how the way cancer is found affects side effects and overall well-being after treatment.
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 research could help doctors understand whether finding breast cancer through screening leads to better quality of life after treatment compared to finding it through symptoms.
- What could go wrong
- This is an observational study, not a treatment trial, so it won't directly change patient care. Results may show differences but cannot prove cause and effect.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
-
4,487 people
The number who actually took part.
- Started
-
Nov 2019
- Finished
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Dec 2025
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population will include women residing in Norway, who are currently alive and were invited and attended, and were invited but did not attend the screening program. Among the attending and not attending women, women who were diagnosed with breast cancer 2006-2017 will be randomly selected. The women diagnosed with breast cancer will be stratified by detection mode (screen-detected versus symptomatic breast cancer). The women within each group will be matched by age. Additionally, women who have never had a diagnosis of breast cancer will be randomly selected from the target population of BreastScreen Norway.
- Ages
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50 to 69 years
- Sex
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Female participants only
- 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.
Study II Inclusion Criteria: * Screened in BreastScreen Norway and diagnosed with breast cancer between 2006 and 2017 * Diagnosed with symptomatic breast cancer between 2006 and 2017 and never attended screening * Screened in BreastScreen Norway and diagnosed with interval breast cancer between 2006 and 2017 * Screened in BreastScreen Norway and have never been diagnosed with breast cancer Exclusion Criteria: * Death after recruitment Study III Inclusion Criteria: * Screened in BreastScreen Norway and diagnosed with breast cancer between 2006 and 2017 * Screened in BreastScreen Norway and diagnosed with interval breast cancer between 2006 and 2017 * Diagnosed with symptomatic breast cancer between 2006 and 2017 and never attended screening Exclusion Criteria: * Death after recruitment
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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
-
Cancer Registry of Norway
Oslo, Oslo, 0304, Norway
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