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Not yet recruitingNCT07819318C-Raven LDCTUpdated Nov 2, 2026

C-Raven LDCT: Lung Cancer Screening Intervention

An interventional study of Video/Brochure and Video/Brochure/Follow-up Call in Lung Cancer Screening, sponsored by Johns Hopkins University. Not yet recruiting. Open to participants aged 50 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-11-02.

Sponsored by Johns Hopkins University · Not applicable, Interventional, and Screening

Updated Nov 2, 2026Start date movedGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
50 Years to 80 Years
Sex
All
01

Study summary

This study is a three-arm, randomized controlled pilot of a lung cancer screening intervention. The investigators will recruit participants ages 50-80 who are likely to meet lung cancer screening guidelines. After eligibility screening, participants will be randomized to one of three educational interventions regarding lung cancer. Lung cancer screening outcomes will be assessed.

Read the detailed description

Smoking is associated with a dramatically increased risk of lung cancer, with rates 10-40 times higher among those who smoke than among those who do not smoke, with smoking accounting for about 85-90% of all lung cancer cases. Screening for lung cancer with low-dose computed tomography (LDCT) has been shown to significantly reduce lung cancer mortality in high-risk populations. Lung cancer screening with annual LDCT is therefore recommended by the US Preventive Services Task Force (USPSTF) for all adults aged 50 to 80 years with a 20 pack-year history of smoking who currently smoke or have quit within the past 15 years. However, in a nationwide study of individuals eligible for lung cancer screening in 2022, only 18% were up-to-date with the recommended screening.

The investigators propose a three-arm, randomized controlled pilot of a lung cancer screening intervention. Recruitment will be carried out primarily through the electronic health record, with invitations sent to patients aged 50-80 who have a documented history of smoking but no chest CT on file within the past 18 months. The investigators will also partner with community organizations such as senior centers and churches to distribute information about the study.

Potential participants will be screened for eligibility for lung cancer screening. If eligible, the participants will undergo a consent process, complete baseline surveys (demographics, etc.), and be randomized to one of the following three study conditions:

  1. Notification of eligibility for lung cancer screening with a recommendation to discuss with the participant's health care provider
  2. Animated video on shared decision-making for LDCT with accompanying guide, offered as a downloadable PDF or mailed hard copy, per individual preference
  3. Video and guide as in (b), plus a one-on-one call with a community health worker (CHW), 1-2 weeks after viewing the materials

Three months after receiving the intervention, follow-up surveys will be sent to assess attitudes toward and completion of lung cancer screening.

02

Conditions studied

  • Lung Cancer Screening

Keywords

  • tobacco
  • smoking
  • lung cancer
  • cancer screening
03

In context

Smoking

1,509 studies on the registry are indexed under Smoking; 193 are open to participants now.

This study's planned enrollment of 300 is above the median of 115 across 1,164 interventional studies indexed under Smoking.

Browse Smoking studies →

Lead sponsor

Johns Hopkins University is the lead sponsor of 1,815 studies on the registry; 315 are open to participants now.

Of its 208 completed or terminated interventional studies of FDA-regulated products, 144 (69%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Existing record within the Johns Hopkins medical system
  • Age 50-80
  • Current tobacco use OR cessation within the past 15 years
  • 20-pack year history of smoking
  • No chest CT imaging within the past 18 months
  • English speaking
  • Willing to complete the study procedures, which include questionnaires and possibly a follow-up call

Exclusion criteria

Exclusion Criteria:

  • Not meeting eligibility criteria
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
300 participants (estimated)

Study arms

  • No intervention
    Notification of Eligibility

    Participants receive notification of eligibility for lung cancer screening with a recommendation to discuss with their health care provider

  • Experimental
    Video/Brochure

    Participants receive an animated video with accompanying guide.

    Behavioral: Video/Brochure

  • Experimental
    Video/Brochure/Follow-up Call

    Participants receive an animated video video, an accompanying guide, and a call with a community outreach specialist/community health worker.

    Behavioral: Video/Brochure/Follow-up Call

Interventions

  • BehavioralVideo/Brochure

    Brief animated video that covers the basics of lung cancer screening and shows shared decision-making. An accompanying brochure uses images and information from the video to reinforce concepts (delivered via PDF or mail, per participant preference).

  • BehavioralVideo/Brochure/Follow-up Call

    Brief animated video that covers the basics of lung cancer screening and shows shared decision-making. An accompanying brochure uses images and information from the video to reinforce concepts (delivered via PDF or mail, per participant preference). A follow-up call with a community outreach specialist/community health worker is made 1-2 weeks after the initial intervention to check in on participant plans regarding lung cancer screening and to assist with any barriers.

06

What researchers measure

Primary outcomes

  1. Number of Participants with Completion of Lung Cancer Screening

    Self-reported completion of low dose chest CT for lung cancer screening during the study follow-up period

    Time frame: 3 months

Secondary outcomes

  1. Number of Participants with Clinician Discussion on Lung Cancer Screening

    Self-reported conversation with clinician about lung cancer screening during the study follow-up period

    Time frame: 3 months

  2. Number of Participants with Change in Intent to obtain lung cancer screening

    Change in intent to obtain lung cancer screening

    Time frame: 3 months

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Start date
Oct 15, 2026→Dec 1, 2026
Nov 2, 2026
Show all 1 update
  1. Nov 2, 2026
    Start date Oct 15, 2026→Dec 1, 2026
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07819318
Collaborators
Maryland Cigarette Restitution Fund
Responsible party
Sponsor
First posted
Sep 14, 2026
Start date
Dec 1, 2026 (estimated)
Primary completion
Jun 30, 2027 (estimated)
Completion
Aug 30, 2027 (estimated)
Last update
Nov 2, 2026

Study contacts

Alejandra Ellison-Barnes, MD, MPH
Contact
aelliso6@jhmi.edu
410-955-5000
Heidi Hutton, PhD
Contact
hhutton@jhmi.edu
443-287-2874
Alejandra Ellison-Barnes, MD, MPH
principal investigator · Johns Hopkins University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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