Rural Illinois Lung Cancer Screening Initiative

ConditionLung Cancer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50-80
SponsorSouthern Illinois University

About this trial

The role of this observational study is to access the feasibility of providing lung cancer screening using a designated nurse navigator through lung cancer screening clinic. Eligible participants will be identified using medical records, eligibility will be confirmed through phone call, screening visits will be scheduled as in-person visit or telehealth visit. Computed tomography screening will be performed at an approved center closer to the individuals place of living and results will be discussed during follow-up in-person visit or telehealth visit.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

All individuals 50-80 years of age

20 pack-year smoking history

Disqualifiers

Individuals 49 years and below or 81 years and above

Has not smoked in 15 or more years

Individuals who develop a health problem that makes them unwilling or unable to have surgery if lung cancer is detected.

Trial population

The risk of lung cancer increases with age and smoking status and hence this age range is recommended for receiving lung cancer screening. As per USPSTF criteria our screening initiative will include individuals 50-80 years, subjects of all sex/gender and all race/ethnic groups. Screening eligible individuals included in our pilot study consisted of 54.4 % women, 75% of non-Hispanic whites, 24% non-Hispanic blacks and 1.2% belonged to 'other' race category. Non-Hispanic black individuals with smoking history have a higher risk of developing lung cancer than a non-Hispanic white. Very few Hispanic persons and women tend to accumulate fewer pack-years over a long period of time.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

10,000 Participants
are grouped into 2 trial groups
Group A: Telehealth cohort
Group B: In-person cohort

Trial outcomes

Primary outcomes

1

Screening rate

Percentage of individuals screened (completed CT imaging) with and without telehealth

Time frame
Through study completion, an average of 1 year
2

Early stage diagnosis

Percentage of individuals diagnosed with lung cancer at an early stage of the disease

Time frame
Through study completion, an average of 1 year

Secondary outcomes

1

Time to treatment initiation

Number of days from diagnosis to treatment initiation will be calculated for each patient diagnosed with lung cancer

Time frame
Through study completion, an average of 1 year
2

Adherence to Screening

Percentage of of individuals undergoing yearly screening with and without telehealth

Time frame
Through study completion, an average of 1 year
3

Cost

Overall cost from pre-screening to screening and follow-up with and without telehealth

Time frame
Through study completion, an average of 1 year

Other outcomes

Sponsors and contacts

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