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Our long-term goal is to integrate non-small cell lung cancer patient treatment preferences into clinical treatment planning.
Full description
The following specific aims are proposed:
Aim 1: Determine whether individual patients' preferences, characteristics, and treatment experiences affect the definition of treatment success.
Aim 2: Determine how to best predict real-life patients' treatment choices based on patients' preferences of adverse events.
Aim 3: Determine whether physicians are likely to change their oncologic clinical practice after receiving a detailed communication of their patients' preferences of adverse events.
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Inclusion criteria
Willing and able to provide consent
Greater than or equal to 19 years of age
Diagnosed with stage IV non-small cell lung cancer (NSCLC)
Able to understand spoken English
Eligible to undergo chemotherapy for stage IV NSCLC, to include, but not limited to, those who:
Exclusion criteria
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Central trial contact
KM Munirul Islam, MD, PhD
Data sourced from clinicaltrials.gov
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