Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06124508

PromotinG Lung Cancer screenIng Awareness and Implementation in Hispanics/Latinx Head and Neck canceR Survivors

Led by University of Miami · Updated on 2026-04-28

44

Participants Needed

1

Research Sites

263 weeks

Total Duration

On this page

Sponsors

U

University of Miami

Lead Sponsor

L

LUNGevity Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to assess the awareness of eligibility of lung cancer screening in Hispanic/LatinX Head and Neck Cancer (HNC) survivors using a survey questionnaire; and to understand the barriers to screening using qualitative interviews.

CONDITIONS

Official Title

PromotinG Lung Cancer screenIng Awareness and Implementation in Hispanics/Latinx Head and Neck canceR Survivors

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Able to understand and sign informed consent
  • Age 18 years or older
  • Self-identify as Hispanic/LatinX
  • Head and neck cancer survivors treated locally with surgery, radiation alone, or definitive chemoradiation at least 5 years ago with no signs of recurrence
  • Meet lung cancer screening eligibility according to USPSTF21 and/or NCCN guidelines (including smoking history and age)
Not Eligible

You will not qualify if you...

  • Diagnosed with lung cancer
  • Current diagnosis of any active malignancy
  • Underwent lung imaging within the previous 3 years
  • Pregnant or nursing mothers
  • Received head and neck cancer treatment less than 5 years before screening
  • Smoking history of less than 20 pack years
  • Previous history of distant metastatic head and neck cancer

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Miami

Miami, Florida, United States, 33136

Actively Recruiting

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Research Team

C

Coral Olazagasti, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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