Tailoring Shared Decision Making for Lung Cancer Screening in Persons Living With HIV

Fred Hutchinson Cancer Center (FHCC)

Status: Completed

Conditions: Lung Carcinoma

Treatments: Other: Interview; Behavioral: Behavioral Intervention; Other: Survey Administration; Other: Discussion (feedback on SDM); Other: Discussion (focus group)

Study type: Observational

Funder types: Other; NIH

Identifiers

NCT04682301

NCI-2020-08393 (Registry Identifier)

RG1121165

P30CA015704 (U.S. NIH Grant/Contract)

10557 (Registry Identifier)

Details and patient eligibility

About

This study tailors a shared decision making intervention for lung cancer screening in persons living with human immunodeficiency virus (HIV). Information collected in this study may help doctors better understand how to perform lung cancer screening in persons living with HIV, so as to enhance shared decision making in persons living with HIV.

Full description

OUTLINE:

AIM I: Participants attend a focus group over 1-1.5 hours providing feedback on refining potential methods of shared decision making (SDM).

AIM II: Participants receive the SDM intervention developed in Aim I and provide feedback. Participants may attend a telephone interview over 45 minutes 1 month later.

Enrollment: 102 patients

Sex: All

Ages: 50+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• AIM I: Patients with human immunodeficiency virus (PWH) enrolled in the local UW HIV cohort and primary providers at Madison Clinic and other Seattle-based clinics serving PWH
• AIM I: Using proposed United States Preventive Services Task Force (USPSTF) guidelines, participants enrolled in the registry who are current or former smokers, report >= 20 pack-years smoking history, and >= 50 years old (n=165) will be eligible for recruitment
• AIM I: Clinicians (medical doctors, physicians assistants and nurse practitioners) who provide primary care for PWH (n=48) will be eligible
• AIM II: PWH who are eligible for lung cancer screening (LCS) based on proposed USPSTF criteria

Exclusion criteria

• Those found to be ineligible for LCS on coordinator review
• Are non-English speaking or have cognitive dysfunction that would prevent participation in SDM

Trial design

102 participants in 1 patient group

Aims I-II

Description:

AIM I: Participants attend a focus group over 1-1.5 hours providing feedback on refining potential methods of SDM. AIM II: Participants receive the SDM intervention developed in Aim I and provide feedback. Participants may attend a telephone interview over 45 minutes 1 month later.

Treatment:

Other: Interview

Other: Survey Administration

Other: Discussion (feedback on SDM)

Behavioral: Behavioral Intervention

Other: Discussion (focus group)