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A Patient and Provider Intervention to Address Health Disparities in Lung Cancer Screening

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Georgetown University

Status

Enrolling

Conditions

Lung Cancer

Treatments

Behavioral: Provider Prompt & Patient Outreach and Education

Study type

Interventional

Funder types

Other

Identifiers

NCT04675476
STUDY00003277

Details and patient eligibility

About

To test the impact of a multilevel intervention on primary (provider-patient communication, intentions, and knowledge) and secondary (screening referrals and completion) outcomes.

Full description

The proposed study will target two key levels of influence in the healthcare setting: provider and patient behavior in order to address disparities between African American and whites in lung screening awareness and utilization. Guided by NIH's Health Disparities Research Framework and building on the formative work conducted in the K99 phase, we will conduct a quasi-experimental study (pretest-posttest, with a nonequivalent control group) in partnership with four primary care clinics within the MedStar Health system in the R00 phase.

Enrollment

368 estimated patients

Sex

All

Ages

50 to 80 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Screening

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

368 participants in 2 patient groups

Multilevel Intervention
Experimental group
Treatment:
Behavioral: Provider Prompt & Patient Outreach and Education
Nonequivalent Control Group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Randi M Williams, PhD

Data sourced from clinicaltrials.gov

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