Small Cell Lung Cancer Community Engagement to Eliminate Research Discepancies
Trial Parameters
Brief Summary
This study will evaluate if a direct-to-patient, de-centralized, remote approach will improve clinical research outreach and engagement for patients with SCLC, in the context of a bio-specimen collection study. The study will also assess self-reported preferences and needs of patients with SCLC, regarding choosing and accessing novel therapies in research or standard clinical care settings and supportive gaps in this area, through an initial and 3 month follow up survey.
Eligibility Criteria
Inclusion Criteria: 1. Men or women greater than or equal to 18 years of age at the time of consent 2. Ability to read, write and communicate in English 3. Provide voluntary consent to participate in this study, documented via a signed informed Consent Form (ICF) 4. Willing to provide clinical and medical information related to his/her cancer diagnoses to the study team as required 5. Willing to comply with the requirements of the study 6. Diagnosis of extensive stage primary SCLC or tSCLC Exclusion Criteria: 1. Known existence of an uncontrolled intercurrent illness including, but not limited to, psychiatric illness or social situations that would impair compliance with study requirements 2. Subjects who previously enrolled to this study Note: Concurrent enrollment in other clinical trials is NOT exclusionary