NCT06486428 · Addario Lung Cancer Medical Institute
Small Cell Lung Cancer Community Engagement to Eliminate Research Discepancies
(SUCCEED)
What this study is about
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.
View original scientific description
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.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Men or women greater than or equal to 18 years of age at the time of consent
- Ability to read, write and communicate in English
- Provide voluntary consent to participate in this study, documented via a signed informed Consent Form (ICF)
- Willing to provide clinical and medical information related to his/her cancer diagnoses to the study team as required
- Willing to comply with the requirements of the study
- Diagnosis of extensive stage primary SCLC or tSCLC
Exclusion criteria
- Known existence of an uncontrolled intercurrent illness including, but not limited to, psychiatric illness or social situations that would impair compliance with study requirements
- Subjects who previously enrolled to this study Note: Concurrent enrollment in other clinical trials is NOT exclusionary
Where
- Multiple Locations, Alabama
- Multiple Locations, Alaska
- Multiple Locations, Arizona
- Multiple Locations, Arkansas
- Multiple Locations, California
- Multiple Locations, Colorado
- Multiple Locations, Connecticut
- Multiple Locations, Delaware
- Multiple Locations, District of Columbia
- Multiple Locations, Florida
- Multiple Locations, Georgia
- Multiple Locations, Hawaii
And 40 more locations — see the full list below.
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Aug 1, 2025 · Source of record for eligibility and locations