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NCT06338592Completed

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

The MyLungHealth Study Protocol: A Pragmatic Patient-Randomized Controlled Trial to Evaluate a Patient-Centered, Electronic Health Record-Integrated Intervention to Enhance Lung Cancer Screening in Primary Care

Source: ClinicalTrials.gov · Last updated 27 Mar 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
31303 (actual)
First submitted
18 Mar 2024
Start date
28 Mar 2024
Primary completion date
27 Mar 2025
Lead sponsor
University of Utah
Diseases
Lung cancer
NCT number
NCT06338592

What you commit to

  • Study type: Interventional
  • Participants enrolled: 31303
  • From 28 Mar 2024 to the primary completion date, 27 Mar 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • A lung cancer diagnosis at the start of the study

Other

  • \>0 but \< 10 pack-year smoking history or quit more than 15 years ago
  • No use of the patient portal at least once in the year preceding the start of the study
  • 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
  • Exposed to the intervention during the pilot phase
  • No visit at a study clinic during the trial period when the intervention was available

Who the study is looking for

  • aged 50-79
  • a history of smoking (e.g., current or former tobacco use)
  • seen in a study primary care clinic in the 12 months preceding the start of the trial
  • 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
  • at least a 20 pack-year smoking history and are a current smoker or have quit within the last 15 years

Age in the registry: 50 years to 79 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
NYU Langone Health
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
University Of Utah Health
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.