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Registry Trial for Young-onset Lung Cancer Patients

This observational study is looking at the experiences of people aged 18 to 50 who have lung cancer. We want to understand how a special care program (called YOLC) affects your satisfaction with your care. We also want to learn about the unique needs of young lung cancer patients and their families, and how joining peer support groups might help. You would be asked to complete surveys at different times over several years to share your experiences. The goal is to see if the YOLC program improves satisfaction and to better understand the journey of young adults with lung cancer.

Study design
This is an observational study, meaning participants will be surveyed without receiving a specific treatment from the study. It aims to enroll 75 participants.
What's involved
You would complete an intake survey and then repeat surveys at 3, 6, 9, 12, 18, 24, 36, 48, and 60 months.
Compensation
Not stated in the trial record.
Follow-up
You would be followed for an average of 5 years, with surveys continuing up to 60 months (5 years).

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07220096

Registry Trial and Needs Assessment of Patients With Young-onset Lung Cancer: Impact of a Dedicated Care Program on Patient Experience and Outcomes

Recruiting
Not specifiedAges 18–50Observational
M.D. Anderson Cancer Center
~75 participants
Updated 2026-04-16 on ClinicalTrials.gov
What's tested:Survey

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Participant satisfaction with care
Measured over Through study completion; an average of 5 year

Conditions

Lung Cancer

Explore related trials

Lung Non-Small Cell Carcinoma

Where it's being run

1 sites across 1 states
Texas1

Study leadership

  • Eric Singhi, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

Who to contact

Eric Singhi, MD
[email protected]
713-745-2263
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Age greater than 18 years and under 50 years
Histologic confirmation of NSCLC
Able to complete an English-language survey independently or with the assistance of a native-language interpreter
Pregnant women- may be enrolled due to age range of subjects. (Low risk)

Exclusion

Medical, psychiatric, cognitive, or other conditions that compromise the patient's ability to understand the patient information, to give informed consent, to comply with the study protocol or to complete the study.
The following special patient population will be excluded from study group:
Individuals who are not yet adults (infants, children, teenagers)
Prisoners
Cognitively-impaired adults

What this trial measures

  • Participant satisfaction with careThrough study completion; an average of 5 year

    Assessed via validated survey instruments (e.g., FACT-L, COST-FACIT). • Focus on detecting even small changes in survey responses over time (baseline, 3, 6, 9, 12 months, etc.).