Can a mobile app plus a breast model teach women to fight cancer fatalism?
NCT ID NCT07828119
First seen Sep 18, 2026 · Last updated Sep 18, 2026
Summary
Researchers test a hybrid breast cancer education program for women aged 20 to 65 who visit an obstetrics and gynecology clinic. The program combines a face-to-face session using a breast model with four weeks of educational messages and reminders sent through a mobile app. The trial measures changes in breast cancer awareness, fatalism, and self-compassion to see if this approach improves early diagnosis awareness and emotional well-being.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a hybrid breast cancer education program combining a face-to-face session with a mobile app
- What this could lead to
- If it works, this could offer a low-cost way to boost breast cancer awareness and reduce fatalistic beliefs, helping women seek earlier diagnosis.
- What could go wrong
- The trial is small and measures attitudes and knowledge, not whether women actually get screened or survive longer. Education alone may not change deep-seated beliefs or access to care.
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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About 128 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
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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20 to 65 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.
Inclusion Criteria: * Being between 20 and 65 years of age * Being female * Agreeing to participate in the study and signing the informed consent form * Having no prior diagnosis of breast cancer * Having the ability to use a mobile application Exclusion Criteria: * Having a prior diagnosis of breast cancer or active breast pathology * Having any cognitive, mental, or communication barrier that prevents participation in training * Refusing to participate or withdraw consent during the study
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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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Kahramanmaras Sutcu Imam University Hospital, Department of Obstetrics and Gynecology, Delivery Room
Kahramanmaraş, Merkez, 46040, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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