Lung Cancer Clinical Trial

The MyLungHealth Study Protocol: Engaging Patients to Enable Interoperable Lung Cancer Decision Support at Scale

Summary

Early lung cancer screening (LCS) through low-dose computed tomography (LDCT) is crucial but underused due to various barriers, including incomplete or inaccurate patient smoking data in the electronic health record and limited time for shared decision-making. The objective of this trial is to investigate a patient-centered intervention, MyLungHealth, delivered through the patient portal. The intervention is designed to improve LCS rates through increased identification of eligible patients and informed decision making.

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Full Description

MyLungHealth is a multi-site pragmatic trial, involving University of Utah Health and New York University Langone Health primary care clinics. The MyLungHealth intervention was developed using a user-centered design process, informed by patient and provider focus groups and interviews. The intervention's effectiveness will be evaluated through a patient-randomized trial, comparing the combined use of MyLungHealth and DecisionPrecision+ (a provider-focused clinical decision support and shared decision-making intervention) against DecisionPrecision+ alone.

View Eligibility Criteria

Eligibility Criteria

Inclusion criteria for both study 1 and study 2:

aged 50-79
a history of smoking (e.g., current or former tobacco use)
use of the patient portal at least once in the year preceding the start of the study
seen in a study primary care clinic in the 12 months preceding the start of the trial

Exclusion criteria for both study 1 and study 2:

a lung cancer diagnosis at the start of the study
>0 but < 10 pack-year smoking history or quit more than 15 years ago

Inclusion criteria for study 1:

a 10-19 pack-year smoking history, an unknown pack-year history, unknown quit date for patients who quit smoking, or a 0 pack-year smoking history

Inclusion criteria for study 2:

at least a 20 pack-year smoking history and are a current smoker or have quit within the last 15 years

Exclusion criteria for study 2:

LDCT completed in the past 3 years
Another chest CT completed in the past year
Structured EHR data indicating LCS SDM was provided in the past 3 years

Study is for people with:

Lung Cancer

Estimated Enrollment:

42415

Study ID:

NCT06338592

Recruitment Status:

Recruiting

Sponsor:

University of Utah

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There are 2 Locations for this study

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NYU Langone Health
New York New York, 10016, United States More Info
Devin Mann, MD
Contact
[email protected]
Devin Mann, MD
Principal Investigator
University of Utah Health
Salt Lake City Utah, 84112, United States More Info
Kensaku Kawamoto, MD, PhD, MHS
Contact
[email protected]
Kensaku Kawamoto, MD, PhD, MHS
Principal Investigator

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Estimated Enrollment:

42415

Study ID:

NCT06338592

Recruitment Status:

Recruiting

Sponsor:


University of Utah

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