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Coping With Glioblastoma: A Study of Communication Between Physicians, Patients, and Caregivers

Coping With Glioblastoma: A Study of Communication Between Physicians, Patients, and Caregivers

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02375841
Enrollment
309
Registered
2015-03-03
Start date
2015-02-01
Completion date
2027-02-01
Last updated
2026-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Cancer, Glioblastoma

Keywords

Communication, Physicians, Patients, Caregivers, 15-034

Brief summary

The purpose of this study is to learn more about the way physicians communicate with brain tumor patients. This study will look at how oncologists provide information about brain tumors, brain scan results, and treatment options. This study will look at how oncologists provide information about brain tumors, brain scan results, and treatment options. Ultimately, the investigators hope to use these findings to improve communication between patients, caregivers and their doctors.

Interventions

BEHAVIORALpsychometric tests, questionnaires and neurocognitive assessments

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER
Weill Medical College of Cornell University
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
number of responses from patients, to 3 yes/no questions2 yearsThe curability of the patient's cancer (curability) The patient's prognosis (prognosis)The patient's goals of care should his/her condition worsen and he/she becomes critically ill (EOL)
number of responses from caregivers to 3 yes/no questions2 yearsThe curability of the patient's cancer (curability) The patient's prognosis (prognosis)The patient's goals of care should his/her condition worsen and he/she becomes critically ill (EOL)
number of responses from physicians to 3 yes/no questions2 yearsThe curability of the patient's cancer (curability) The patient's prognosis (prognosis)The patient's goals of care should his/her condition worsen and he/she becomes critically ill (EOL)

Countries

United States

Contacts

PRINCIPAL_INVESTIGATOREli Diamond, MD

Memorial Sloan Kettering Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026