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NCT06486428Active, not recruiting

Small Cell Lung Cancer Community Engagement to Eliminate Research Discepancies

A Study to Evaluate a Remote, Decentralized, Direct-to-Patient Strategy for Clinical Research Engagement of Patients With Small Cell Lung Cancer (SCLC).

Source: ClinicalTrials.gov · Last updated 4 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
22 (actual)
First submitted
15 Dec 2023
Start date
23 May 2025
Primary completion date
15 Jul 2026
Lead sponsor
Addario Lung Cancer Medical Institute
Diseases
Lung cancer
NCT number
NCT06486428

What you commit to

  • Study type: Observational
  • Participants enrolled: 22
  • From 23 May 2025 to the primary completion date, 15 Jul 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subjects who previously enrolled to this study
    • Note: Concurrent enrollment in other clinical trials is NOT exclusionary

Other illness

  • Known existence of an uncontrolled intercurrent illness including, but not limited to, psychiatric illness or social situations that would impair compliance with study requirements

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
Multiple LocationsUnited StatesUnknown status
Vanderbilt-Ingram Cancer Center
Coordinator of this site? Confirm its status
NashvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.