Can a tablet game sharpen aging minds during breast cancer treatment?
NCT ID NCT04261153
First seen Jul 02, 2026 · Last updated Jul 02, 2026
Summary
This study explores whether a tablet-based cognitive stimulation program called HAPPYNeuron® is practical for breast cancer patients aged 70 and older. Cancer treatments, especially chemotherapy, can cause memory and thinking problems, and older patients may be at higher risk. The study will have participants complete three 20-minute sessions on a tablet to see if they can and will use the software, aiming to find a way to help reduce cognitive side effects and improve 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
- HAPPYNeuron® cognitive stimulation software
- What this could lead to
- If successful, this could point toward a practical, non-drug way to help older breast cancer patients maintain memory and thinking skills during cancer treatment.
- What could go wrong
- This is a small feasibility study, so it cannot prove the software improves cognition. Older patients may find tablet use difficult, and the program may not be widely adopted.
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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55 people
The number who actually took part.
- Started
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Jun 2020
- Finished
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May 2024
- 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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70 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: * Patient with breast cancer, aged 70 and over, * During treatment with chemotherapy, targeted therapy or radiotherapy. * Whatever the stage of the disease, * Hospitalised in a week hospital, in traditional hospitalisation for an intercurrent episode or day hospitalisation, or undergoing radiotherapy * Absence of major cognitive impairment preventing cognitive tests (compliance with the MoCA score threshold based on the patient's age and educational level according to GRECOGVASC standards), * Patient with education level 3 "end of primary education" minimum (Barbizet scale), * Mastery of the French language, * Patient who signed the consent to participate in the study. Exclusion Criteria: * Hospitalization for neurological reasons (e.g. confusion), or psychiatric, * Documented brain metastases, * History of brain radiation therapy, * Progressive psychiatric pathology or known dementia, * Abuse of alcohol or drug use, * Severe visual and / or hearing loss, * Patient's refusal to participate, * Patient deprived of liberty or under guardianship.
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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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Centre François Baclesse
Caen, 14076, France
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Centre Henri Becquerel
Rouen, France
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