- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07227480
Advancing Lung Cancer Screening One Text at a Time
February 16, 2026 updated by: Francisco Cartujano, MD, University of Rochester
The purpose of this study is to assess the feasibility, acceptability, and preliminary impact of text messaging to promote lung cancer screening.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
We will conduct a two-arm pilot randomized controlled trial with 40 adults.
Participants will be randomized in a 1:1 ratio to either UR Screened (a text messaging program designed to promote lung cancer screening) or a control group (a mailed educational material along with a flyer for the lung cancer screening program).
We will assess recruitment and follow-up rates, satisfaction with the program or educational material, and uptake of lung cancer screening at week 12.
Additionally, we will compare screening rates between the intervention and control groups.
Study Type
Interventional
Enrollment (Estimated)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Francisco Cartujano, MD
- Phone Number: (585) 273-1646
- Email: francisco_cartujano@urmc.rochester.edu
Study Locations
-
-
New York
-
Rochester, New York, United States, 14642
- Recruiting
- University of Rochester Medical Center
-
Contact:
- Francisco Cartujano, MD
- Phone Number: 585-353-0035
- Email: francisco_cartujano@urmc.rochester.edu
-
Principal Investigator:
- Francisco Cartujano, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- 50 to 80 years old
- have not completed their annual screening for lung cancer
- have a 20 pack-year smoking history
- currently smoke or have quit within the past 15 years
- speak English and/or Spanish
- have a functioning cellphone number with unlimited text messaging capacity
- be willing to complete a baseline and a follow-up (at Month 3) survey
Exclusion Criteria:
- being up-to-date on their annual lung cancer screening
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: UR Screened
A text messaging program designed to promote lung cancer screening
|
A text messaging program designed to promote lung cancer screening
|
|
Active Comparator: Control group
A mailed educational material along with a flyer for the lung cancer screening program
|
A mailed educational material along with a flyer for the lung cancer screening program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percent of Participants Who Undergo Lung Cancer Screening
Time Frame: Month 3
|
The proportion of study participants who complete a lung cancer screening test within 3 months of study enrollment
|
Month 3
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 17, 2026
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Study Registration Dates
First Submitted
November 10, 2025
First Submitted That Met QC Criteria
November 10, 2025
First Posted (Actual)
November 12, 2025
Study Record Updates
Last Update Posted (Actual)
February 19, 2026
Last Update Submitted That Met QC Criteria
February 16, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- STUDY00010975
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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