Clinicians share insights to shape AI support for breast cancer patients
NCT ID NCT07644845
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study asks 12 clinicians in Florida who care for women with breast cancer about gaps in emotional and mental health support. They will join virtual focus groups and fill out a short survey. The goal is to use their insights to build an AI-powered digital platform called MammoVerse that could offer emotional support, peer connection, and better healthcare engagement.
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 could guide the development of an AI-based digital platform to improve emotional support and peer connection for breast cancer patients.
- What could go wrong
- This is a very small, early-stage study (12 clinicians) that only collects opinions, not patient data. The AI platform is not yet built, so benefits are uncertain.
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 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- 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.
Who is studied
Recruitment will be through targeted outreach to clinicians providing breast cancer care in Florida. Invitations will be distributed via email to University of Central Florida College of Medicine UCF COM faculty, affiliated faculty and clinical partners over the recruitment period. Interested clinicians will be provided with study information and instructions for contacting the research team as well as accessing the online consent and enrollment materials. Interested clinicians will enroll online, and provide their information for scheduling the focus group meeting.
- Ages
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18 years and older
- Sex
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Anyone
- 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: * they are an adult (over 18) * physician (MD or DO), licensed psychologist (PhD or PsyD), advanced practice provider (ARNP or PA), nurse (RN or LPN), licensed clinical social worker (LCSW) or other licensed clinician * provide specialized cancer care to women diagnosed with breast cancer in Florida * can provide informed consent * are self-reporting that they licensed clinicians * are self-reporting that they are physically able to participate in a 60-minute group discussion. Exclusion Criteria: * This study will NOT include persons under the age of 18, prisoners, and persons unable to speak English fluently, and persons unable to provide informed consent. We are not able to accommodate non-English speakers as this is a pilot study involving group discussion.
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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University of Central Florida
Orlando, Florida, 32827, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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