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Lung Non-Small Cell CarcinomaNCT07186699

Qualitative Study on Detection & Tx of NSCLC in Pts w/ a History of Alcohol or SUD

An observational study of Lung Non-Small Cell Carcinoma and Thoracic Cancer, run by University of Southern California at 2 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study will attempt to identify social facilitators and barriers to detection and treatment of non-small cell lung cancer in order to learn how a history of substance abuse or alcohol use impacts care for non-small cell lung cancer. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Non-Interventional Study
How many people
45 participants
Where
2 sitesUnited States
Study dates
29 Sep 2025to 12 Sep 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with thoracic cancers, including lung and esophageal, recruited through USC/Norris Comprehensive Cancer Center

Who may be able to join

  • * Adults ≥ 18 years of age
  • Histopathologic or cytologic diagnosis of thoracic cancers, including lung and esophageal
  • Received or receiving curative intent treatment (e.g. surgery, radiation therapy, systemic therapy)
  • Ability to understand and the willingness to sign a written informed consent
  • English or Spanish speaking. Due to need to conduct semi-structured interviews which can develop into free-flowing conversations we need both participant and interviewer to be fluent

Who cannot join

  • Patients with cognitive disability unable to maintain 30-60 minute conversation

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

United States2 sites, 2 recruiting
  • Los Angeles General Medical Center

    Los Angeles, California, 90033

    Sandy Tran, 323-865-3935, sandy.tran@med.usc.edu

    Brooks V. Udelsman

    Recruiting
  • USC / Norris Comprehensive Cancer Center

    Los Angeles, California, 90033

    Sandy Tran, 323-865-3935, sandy.tran@med.usc.edu

    Brooks V. Udelsman

    Recruiting

Other trials in United States

About this study

Official title: Qualitative Study on Detection and Treatment of Thoracic Malignancies in Patients With a History of Alcohol or Substance Use Disorder

This study will attempt to identify social facilitators and barriers to detection and treatment of non-small cell lung cancer in order to learn how a history of substance abuse or alcohol use impacts care for non-small cell lung cancer.

Read the detailed description

PRIMARY OBJECTIVE:

  1. To identify social facilitators and barriers to detection and treatment of thoracic cancers by interviewing a diverse group of patients at Keck, Los Angeles General Medical Center, and Norris Cancer Center with alcohol or substance use disorder history.

OUTLINE: This is an observational study.

Patients participate in a semi-structured interview and may participate in a follow-up focus group interview in which preliminary findings are shared and feedback is elicited on study.

Being tested
Non-Interventional Study
Medical subject headings
Carcinoma, Non-Small-Cell Lung

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Non-Interventional StudyOther

    Also called Non-Interventional Observational Study, Noninterventional (Observational) Study

    Non-interventional study

Study groups in NCT07186699
Study groupRoleWhat they receive
ObservationalPatients participate in a semi-structured interview and may participate in a follow-up focus group interview in which preliminary findings are shared and feedback is elicited on study.
Receives: Other: Non-Interventional Study

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Thematic saturation

    Will use a Danaher framework to approach analyze interview data using NVivo software (NVivo version 11.0, QSR International). Each interview will be analyzed to identify broad themes.

    Measured: Up to 3 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Sep 2025
  2. Study start29 Sep 2025
  3. Primary completion12 Sep 2027 (estimated)
  4. Study completion12 Sep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
45 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07186699
Sponsor's protocol ID
2N-25-7
Other IDs
NCI-2025-05477, 2N-25-7, P30CA014089
Status last verified
Sep 2026
First submitted
10 Sep 2025
Last updated
22 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Lung Non-Small Cell Carcinoma and Thoracic Cancer, run by University of Southern California at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 22 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Thematic saturation (time frame: Up to 3 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Sep 2026.

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