A Patient and Provider Intervention to Address Health Disparities in Lung Cancer Screening
Recruiting · NCT04675476 · Interventional (participants receive a specific treatment) · Lead sponsor: Georgetown University
View the official record on ClinicalTrials.gov →Interventions studied
Provider Prompt & Patient Outreach and Education
What this trial is about
To test the impact of a multilevel intervention on primary (provider-patient communication, intentions, and knowledge) and secondary (screening referrals and completion) outcomes.
Who can take part
Age range
50 Years to 80 Years
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- 50-80 years old;
- current cigarette smoker or quit within 15 years;
- a 20+ pack-year smoking history;
- non-adherent to lung screening (\>13 months);
- English-speaking;
- scheduled for an upcoming clinic appointment (4 weeks - 8 weeks); and
- able and willing to provide meaningful consent and complete telephone interviews
Exclusion criteria
- Individuals with a history of lung cancer
Where it is running
1 location listed across 1 US state.
- MedStar Health - Washington D.C., District of Columbia, United States