New digital platform aims to break the silence around hereditary cancer in families
NCT ID NCT04214210
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a digital health platform to help people with a hereditary risk of breast and ovarian cancer share their genetic test results with family members. Researchers worked with 128 participants in Switzerland and Korea to see if the tool reduced distress and improved communication. The goal was to make it easier for relatives to learn about their own cancer risk and get tested.
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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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128 people
The number who actually took part.
- Started
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Apr 2022
- Finished
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Dec 2025
- 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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19 to 99 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Speak and read German, French, Italian, English, or Korean * Residence in Switzerland or in Korea * Has been identified with a pathogenic variant associated with HBOC or * Has ≥1 first-, second-degree relative or first cousing with HBOC * Mentally able to provide informed consent Exclusion Criteria: * mutation carriers who do not have any family members; * husbands and partners, although they may play an important role in decisions for genetic testing and risk management of disease, will not be included in the study; * participants with a prior diagnosis of a mental disease and those unable to provide informed consent; * those physically ill and not being able to complete a baseline survey; * those without access to the web through a computer, tablet, or smartphone.
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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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HFR Fribourg - Hôpital cantonal
Fribourg, Canton of Fribourg, 1752, Switzerland
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Hirslanden Clinic Des Grangettes
Geneva, Canton of Geneva, 1224, Switzerland
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Hopital du Jura - Service d' Oncology
Delémont, Canton of Jura, 2800, Switzerland
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Istituto Oncologico della Zvizzera Italiana
Bellinzona, 6962, Switzerland
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Kantonalspital Winterthur
Winterthur, Canton of Zurich, 8401, Switzerland
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Unite d'Oncogenetique et de Prevention des Cancers
Geneva, 1205, Switzerland
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Universitatklinik fur Medizinische Onkologie, Inselspital
Bern, 3010, Switzerland
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University Hospital Basel
Basel, 4056, Switzerland
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Retrospective analysis of pyrotinib in the treatment of HER2-Positive advanced breast cancer previously treated with trastuzumab and pertuzumab
- Operationalising multifactorial ovarian cancer risk assessment using the CanRisk tool versus standard practices.
- Can a new drug shrink advanced solid tumors?
- Mind and body: does resilience leave a molecular mark in breast cancer?
- Which pain block works better for breast surgery?
- Can a Triple-Drug combo erase HER2-Positive breast tumors before surgery?