Video chat with nurse may ease brain cancer anxiety before treatment
NCT ID NCT06485310
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a teleconsultation with a specially trained nurse can reduce psychological distress in adults recently diagnosed with a primary brain tumor. 58 participants will be randomly assigned to receive either usual care or usual care plus one nurse-led video call before their first cancer treatment. The goal is to see if the extra support improves distress, anxiety, and quality of life scores.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nurse-led teleconsultation for psychological support
- What this could lead to
- If it works, this could provide a simple, remote way to reduce distress for brain cancer patients before starting treatment.
- What could go wrong
- This is a small, early-stage trial (58 participants) testing a support service, not a treatment. The benefit may be small or 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 58 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
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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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: * aged 18 and over * being treated for a primary malignant tumor of the central nervous system (positive biopsy) * with a Mini-Mental State score greater than 24 * not receiving first-line treatment (chemotherapy, targeted radiotherapy, surgery) * with a distress score above 3 on the Psychological Distress Thermometer * have access to computer equipment equipped with a microphone and webcam (smartphone, computer) * able to read, write and speak French * have given free and informed consent * being affiliated to a social security scheme Exclusion Criteria: * with a history of psychiatric illness * with recurrent cancer of the cerebral nervous system * having begun first-line treatment (drug therapy, curative surgery, radiotherapy or palliative care) * under guardianship, curatorship or deprived of liberty
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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
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.
Contacts and locations
Locations
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University Hospital of Reunion Island - Neurosurgery department
Saint-Pierre-des-Corps, Reunion, 97410, France
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