Can an online tool help older cancer patients stay connected to their care team?
NCT ID NCT04913259
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This pilot study tests whether elderly cancer patients (65 and older) can use an online tool to regularly report symptoms and quality of life during treatment. Over 3 months, patients fill out weekly questionnaires on side effects and two longer surveys on well-being. The goal is to see if this kind of remote monitoring is practical and helpful for this age group.
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 show that remote monitoring is feasible for older cancer patients, potentially leading to better symptom management and quality of life during treatment.
- What could go wrong
- This is a small pilot study with only 33 participants, so results may not apply to all patients. The tool may be too complex for some elderly users, and the study does not test whether it improves health outcomes.
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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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33 people
The number who actually took part.
- Started
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Jun 2021
- Expected to finish
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Jun 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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65 years and older
- 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.
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: 1. Patients 65 years of age and over. 2. Histologically proven cancer: breast, lung, ovary, prostate, bladder, kidney, ear-nose-throat, colon-rectum, melanoma, sarcoma, lymphoma, myeloma, or myelodysplastic syndrome. 3. Included before starting medical treatment (chemotherapy, hormone therapy, targeted therapy, immunotherapy or combination). 4. Informed consent dated and signed. 5. Patients affiliated with a French social security scheme in accordance with the French law on biomedical research (Article 1121-11 of the French Code of Public Health). Exclusion Criteria: Life expectancy less than 12 months. 2. Patient declining to use a tablet, computer, mobile phone or the Internet. 3. Patient not knowing how to read and understand French. 4. Technical impossibility of connecting to the Internet in the patient's living area. 5\. Patient already included in this study or in another study evaluating a remote monitoring system.
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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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Institut Bergonie
Bordeaux, 33600, France
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