Smartphone app aims to ease chemotherapy symptoms for breast cancer patients
NCT ID NCT07200791
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a mobile app can help women with breast cancer better manage side effects from chemotherapy, like fatigue, nausea, and sleep problems. 74 patients will either use the app plus standard care or receive standard care alone. The app includes symptom tracking, short educational videos, and direct contact with a nurse. Researchers will measure changes in symptom severity and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- mobile application
- What this could lead to
- If it works, this could give breast cancer patients a simple, app-based way to track and ease chemotherapy side effects at home.
- What could go wrong
- This is a small, early-stage trial (74 people) testing a behavioral tool, not a drug. The app may not significantly improve symptoms or quality of life, and results may not apply to all patients.
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 74 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Aug 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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18 years and older
- Sex
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Female participants only
- 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: * 18 yaş ve üzerinde olan, * Çalışmaya katılmayı kabul eden, * Meme kanseri tanısı alan kadınlar, * 4AC-12 Paklitaksel tedavi protokolü uygulana, * Okuma yazma bilen ve iletişim problemi olmayan, * Akıllı telefonu olan bireyler * Akıllı telefonu kullanabilen bireyler * Verileri eksiksiz olarak dolduran bireyler Exclusion Criteria: * Kardiyak problemi olan bireyler * Karaciğer ve böbrek yetmezliği olan bireyler * Mobil uygulama kullanamayan bireyler * Akıllı telefon kullanamayan bireyler * Araştırmadan ayrılmak isteyen bireyler * Araştırmada çeşitli sebeplerle eksik veri toplanan bireyler
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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 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.
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Other studies related to the condition(s) this trial covers.
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