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SuspendedNCT04926662Updated Sep 8, 2026

Understanding Rural Patient and Provide Preferences for Mobile Lung Cancer Screening Clinics

An observational study in Lung Cancer, sponsored by Dartmouth-Hitchcock Medical Center. Suspended at 1 site in United States. Open to participants aged 50 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-09-08.

Sponsored by Dartmouth-Hitchcock Medical Center · Observational

Why this study was suspended
Study is paused while pre-aim 1 work is being done
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
320
Ages
50 Years to 80 Years
Sex
All
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Study summary

The purpose of this study is to research patient preferences for lung cancer screening and pilot mobile units to address the barrier of access that decreases participation in lung cancer screening.

Read the detailed description

The overarching goal of this study is to research patient preferences for lung cancer screening and pilot mobile units to address the barrier of access that decreases participation in lung cancer screening. To facilitate this, the investigators will evaluate the feasibility of mobile lung cancer screening clinics to improve access through focus group study in designated rural areas of New Hampshire and Vermont, canvas and survey these areas to confirm need, and pilot the mobile lung cancer screening clinic to establish practicability. Findings from the proposed project will be used as preliminary data to apply for further funding and to implement the mobile unit in these identified rural communities on a consistent basis.

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Conditions studied

  • Lung Cancer

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03

In context

Lung Neoplasms

7,243 studies on the registry are indexed under Lung Neoplasms; 1,557 are open to participants now.

This study's planned enrollment of 320 is above the median of 189 across 1,514 observational studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

Dartmouth-Hitchcock Medical Center is the lead sponsor of 472 studies on the registry; 68 are open to participants now.

Of its 30 completed or terminated interventional studies of FDA-regulated products, 20 (67%) have results posted.

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

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Who can participate

Ages eligible
50 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The individuals that will be included in this study will be those that meet lung cancer screening eligibility.

Inclusion criteria

  • Adults age 50 to 80 years old
  • 20 pack-year smoking history who are currently smoking or have quit smoking within the last 15 years

Exclusion criteria

Exclusion Criteria:

-

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
320 participants (estimated)
Patient registry
No

Groups and cohorts

  • Aim 1: Focus Groups

    Focus groups will be conducted in 2 New Hampshire and 2 Vermont towns to better understand patient knowledge, attitudes, and preferences regarding access to lung cancer screening.

  • Aim 2: Cross Sectional Survey

    Based on focus group feedback, the investigators will visit each proposed site to survey on 2 separate dates to confirm days and times of high traffic. The investigators will also survey patrons at the proposed locations to further determine prospective patient mobile screening preferences and evaluate willingness to participate in screening.

  • Aim 3: Survey with follow up data

    The investigators will pilot mobile lung cancer screening clinics at each chosen location using the knowledge acquired from focus group experience and local patient survey. Surveys will be conducted at these clinics, and patients will be followed for up to 5 years.

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What researchers measure

Primary outcomes

  1. Recruitment

    Number of individuals recruited to the mobile lung cancer screening units

    Time frame: 6 months after starting the mobile lung cancer screening units (Aim 3)

Secondary outcomes

  1. Change in knowledge

    Change in knowledge before and after entering the mobile lung cancer screening, as determined by the pre and post survey

    Time frame: 6 months after starting the mobile lung cancer screening units (Aim 3)

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Study locations

1 site
  • Dartmouth-Hitchcock Medical Center
    Lebanon, New Hampshire 03755, United States
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References and documents

Publications

  • Odahowski CL, Zahnd WE, Eberth JM. Challenges and Opportunities for Lung Cancer Screening in Rural America. J Am Coll Radiol. 2019 Apr;16(4 Pt B):590-595. doi: 10.1016/j.jacr.2019.01.001. PubMed 30947892 ↗
  • Brenner AT, Malo TL, Margolis M, Elston Lafata J, James S, Vu MB, Reuland DS. Evaluating Shared Decision Making for Lung Cancer Screening. JAMA Intern Med. 2018 Oct 1;178(10):1311-1316. doi: 10.1001/jamainternmed.2018.3054. PubMed 30105393 ↗
  • Atkins GT, Kim T, Munson J. Residence in Rural Areas of the United States and Lung Cancer Mortality. Disease Incidence, Treatment Disparities, and Stage-Specific Survival. Ann Am Thorac Soc. 2017 Mar;14(3):403-411. doi: 10.1513/AnnalsATS.201606-469OC. PubMed 28118039 ↗
  • Greenwald ZR, El-Zein M, Bouten S, Ensha H, Vazquez FL, Franco EL. Mobile Screening Units for the Early Detection of Cancer: A Systematic Review. Cancer Epidemiol Biomarkers Prev. 2017 Dec;26(12):1679-1694. doi: 10.1158/1055-9965.EPI-17-0454. Epub 2017 Oct 4. PubMed 28978564 ↗
  • Bhatt S, Isaac R, Finkel M, Evans J, Grant L, Paul B, Weller D. Mobile technology and cancer screening: Lessons from rural India. J Glob Health. 2018 Dec;8(2):020421. doi: 10.7189/jogh.08.020421. PubMed 30603075 ↗
  • Vang S, Margolies LR, Jandorf L. Mobile Mammography Participation Among Medically Underserved Women: A Systematic Review. Prev Chronic Dis. 2018 Nov 15;15:E140. doi: 10.5888/pcd15.180291. PubMed 30447104 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04926662
Lead sponsor
Dartmouth-Hitchcock Medical Center
Responsible party
Dana.M.Ferrari-Light (Staff Physician, Thoracic Surgery, Dartmouth-Hitchcock Medical Center) — Principal investigator
First posted
Jun 15, 2021
Start date
Jul 14, 2021
Primary completion
Jan 1, 2029 (estimated)
Completion
Jun 1, 2029 (estimated)
Last update
Sep 8, 2026

Study contacts

David Finley, MD
principal investigator · Dartmouth-Hitchcock Medical Center

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 suspended, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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