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Recruiting NCT06280300

Multi-disciplinary Care for Brain Metastases

No phase Interventional Brain Metastases, Adult

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: health services intervention.
Who it may be relevant to
Registry conditions: Brain Metastases, Adult. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Intensive Multi-Disciplinary Care Initiative for Patients With Newly Diagnosed Brain Metastases

Overview

This is a health services intervention study aimed at understanding the impact of intensive multi-disciplinary care compared with standard care on patient-reported symptom outcomes and prognostic awareness in patients with brain metastases.

Detailed description

This is a cohort study of patient with newly diagnosed brain metastases assigned to standard of care (SOC) or intensive multi-disciplinary care (IMDC). Care for all patients with brain metastases involves complex medical decision making and requires input for multiple stakeholders, including medical oncology, neurosurgery, radiation oncology, and neuro-oncology. Palliative care should be an essential component of the care team for all patients with brain metastases by the very nature of this advanced malignancy. At the University of Vermont, our current process for diagnosis and management of patients with brain metastases relies heavily on the physician and team who make the initial diagnosis to consult others as they see appropriate. This process may look different for different patients. We rationalize that a systematic approach with intensive multidisciplinary care (IMDC) will benefit patients with brain metastases by providing consistent access to multi-disciplinary discussion.

Interventions

  • Other health services intervention
    Health services intervention

Primary outcome measures

  • Patient reported outcomes [Time frame: 6-12 months]
Secondary outcome measures (3)
  • Feasibility [Time frame: 6-12 months]
  • Patient understanding of prognosis [Time frame: 6-12 months]
  • survival [Time frame: 6-12 months]

Eligibility criteria

Inclusion criteria

  • Patients of all genders must be at least 18 years of age.
  • Patients must have histologically confirmed, newly diagnosed brain metastases from known or suspected solid tumor primary neoplasms.
  • Patients must be able to accurately provide self-report data (e.g. per clinical judgment, cognitive function is intact).
  • Patients must be able to complete questionnaires in English.
  • Patients must have the ability to provide informed consent.

Exclusion criteria

  • Patients who are < 18 years of age are not eligible.
  • Patients who are Pregnant are not eligible.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Health services research

Study locations

United States · 1 center
  • University of Vermont Medical Center — Burlington

Identifiers

NCT: NCT06280300 · UVMMC2203

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗