Brain tumor communication study aims to improve tough talks
NCT ID NCT02375841
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how doctors, patients with glioblastoma (a serious brain cancer), and their caregivers talk about the disease, scan results, and treatment choices. Researchers will use surveys and tests to understand these conversations. The goal is to find ways to improve communication and help everyone make better decisions together.
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 study could help doctors talk more clearly with patients and families about brain tumor care and difficult decisions.
- What could go wrong
- This is an observational study, not a treatment trial. It may not lead to direct changes in care or outcomes.
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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309 people
The number who actually took part.
- Started
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Feb 2015
- Expected to finish
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Feb 2027
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
All patients with GBM will be screened in the outpatient clinic at MSKCC.
- 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: Patient Inclusion Criteria: * 18 years or older * Pathologic diagnosis of WHO grade IV glioma, as per MSKCC medical record or outside medical record. * In the judgment of the consenting professional, proficiency in English that will allow the participant to be able to complete study questionnaires and assessments. Many of the study assessments are available only in English. * At the time of consent, orientation to self, place, month and year Caregiver Inclusion Criteria: * 18 years or older * Identified by the patient as a relative, friend, or partner with whom he or she has a significant relationship and who provides him or her informal (unpaid) care (i.e., physical or emotional assistance). * In the judgment of the consenting professional, proficiency in English that will allow to complete study questionnaires and assessments. Many of the study assessments are available only in English. Oncologist Inclusion Criteria: * Treating Neuro-Oncologist in the Department of Neurology Exclusion Criteria: Patient Exclusion Criteria: * A patient will be excluded if in the opinion of his/her attending neuro-oncologist or the covering neuro-oncologist, he does not have the capacity to consent to the study based on clinical evaluation * Aphasia precluding comprehension and verbalization of consent to participate, in the estimation of the attending physician. Caregiver Exclusion Criteria: * There are no caregiver exclusion criteria.
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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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Henry Ford Hospital
Detroit, Michigan, 48202, United States
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Memorial Sloan Kettering Basking Ridge
Basking Ridge, New Jersey, 07920, United States
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Memorial Sloan Kettering Bergen
Montvale, New Jersey, 07645, United States
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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Memorial Sloan Kettering Commack
Commack, New York, 11725, United States
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Memorial Sloan Kettering Monmouth
Middletown, New Jersey, 07748, United States
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Memorial Sloan Kettering Westchester
Harrison, New York, 10604, United States
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University of Vermont Medical Center
Burlington, Vermont, 05401, United States
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Other studies related to the condition(s) this trial covers.
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