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Recruiting NCT06070870

NCT06070870 Health Education Approach to Lung Screening

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Clinical Trial Summary
NCT ID NCT06070870
Status Recruiting
Phase
Sponsor Virginia Commonwealth University
Condition Lung Cancer
Study Type INTERVENTIONAL
Enrollment 675 participants
Start Date 2023-10-10
Primary Completion 2027-11-30

Eligibility & Interventions

Sex All sexes
Min Age 50 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Patient Navigation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 675 participants in total. It began in 2023-10-10 with a primary completion date of 2027-11-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Evaluate the impact of the patient navigation program on the proportion of patients who complete lung cancer screening (LCS), defined as undergoing a low dose computed tomography (LDCT)

Eligibility Criteria

Inclusion Criteria: * Meets current USPSTF guidelines for lung cancer screening (LCS) * 20 pack-year smoking history Note: A pack-year is a way of calculating how much a person has smoked in their lifetime. One pack-year is the equivalent of smoking an average of 20 cigarettes-1 pack-per day for a year. * Currently smokes or has quit smoking within the past 15 years * Identifies as Black or African-American Note: Both Hispanic/Latino and Non-Hispanic/Latino patients are eligible as long as they also identify as Black or African-American (eg, Afro-Latino). * Willing to complete all navigation-related study activities * Able to understand and the willingness to sign a written informed consent document Exclusion Criteria: A patient who meets any of the following exclusion criteria is ineligible to participate in the study: * Known history of cancer (except squamous cell skin cancer), or coughing up blood in the past 5 years, as reported by the individual * Has undergone a previous lung cancer screening * Inability to speak English * Medical, psychological, or social condition that, in the opinion of the investigator, may increase the patient's risk or limit the patient's adherence with study requirements

Contact & Investigator

Central Contact

Massey IIT Research Operations

✉ masseyepd@vcu.edu

📞 804-628-6430

Principal Investigator

Vanessa Sheppard, PhD

PRINCIPAL INVESTIGATOR

Virginia Commonwealth University

Frequently Asked Questions

Who can join the NCT06070870 clinical trial?

This trial is open to participants of all sexes, aged 50 Years or older, up to 80 Years, studying Lung Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06070870 currently recruiting?

Yes, NCT06070870 is actively recruiting participants. Contact the research team at masseyepd@vcu.edu for enrollment information.

Where is the NCT06070870 trial being conducted?

This trial is being conducted at Carrboro, United States, Charleston, United States, Richmond, United States.

Who is sponsoring the NCT06070870 clinical trial?

NCT06070870 is sponsored by Virginia Commonwealth University. The principal investigator is Vanessa Sheppard, PhD at Virginia Commonwealth University. The trial plans to enroll 675 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology