Night shift workers get tailored cancer prevention plan in new study
NCT ID NCT07630935
First seen Jun 27, 2026 · Last updated Jul 17, 2026 · Updated 4 times
Summary
This study tests whether a personalized prevention plan helps female night shift workers reduce their breast cancer risk. Night shift work is linked to higher cancer risk due to disrupted sleep cycles. One hundred women at a Paris hospital will receive tailored advice on diet, exercise, smoking, alcohol, and screening, then be followed for 5 years to see if they stick with the recommendations.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Personalized Prevention Plan (behavioral intervention: lifestyle, diet, physical activity, smoking, alcohol, screening recommendations)
- What this could lead to
- If successful, this could show that personalized lifestyle advice helps night shift workers lower their breast cancer risk and improve screening habits.
- What could go wrong
- This is a small, early-stage study (100 participants) measuring adherence, not cancer outcomes. Results may not apply to all shift workers, and long-term behavior change is hard to sustain.
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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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Jul 2032
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.
Who is studied
The target population consists of female night staff at Pitié-Salpêtrière Hospital
- Ages
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18 years and older
- 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.
Inclusion Criteria: * Female participants aged 18 years or older * Night shift workers at Pitié-Salpêtrière Hospital * Attending consultation for breast cancer risk assessment PGRC * Affiliated with a social security system * No personal history of breast cancer * Provided informed consent (non-opposition procedure according to French regulations) Exclusion Criteria: * Pregnant or breastfeeding women * Individuals under legal protection or deprived of liberty * Individuals without standard health insurance coverage
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Pitié Salpêtrière hospital
RECRUITINGParis, 75013, France
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