TELEhealth Shared decision-making COaching for lung cancer screening in Primary care (TELESCOPE) for Hispanics.
The primary objective is to explore the impact of a culturally adapted TELESCOPE intervention vs. EUC on the initial uptake of LDCT.
The Secondary objective is to compare the quality of the shared decision-making (SDM) process for lung cancer screening between the culturally adapted TELESCOPE intervention vs. EUC.
- Rutgers University
Inclusion Criteria: Aim 1 (Cultural Adaptation): To be eligible, patients must: 1. Identify as Hispanic and/or Latino(a) 2. Able to read and speak in English or Spanish 3. Be 50 to 77 years of age 4. Be a current or former smoker 5. Have at least a 20-pack-year smoking history Aims 2-3 (Pilot Randomized Controlled Trial) To be eligible, patients must: - Identify as Hispanic or Latino(a) - Able to speak and read in English or Spanish - Be 50 to 77 years of age - Be a current or former smoker having quit within the past 15 years - Have at least a 20 pack-year smoking history - Be scheduled for a non-acute care visit at one of the study sites. - Not coughing up blood in the last two weeks Interviews Providers completing the semi-structured interviews will be: - A practicing primary care clinician or a clinic director (n=20), nursing director, or clinic practice administrator at one of the participating sites, or a TELESCOPE study patient navigator and nurse navigator - Age 18 or older - Fluent in English Online surveys Providers completing online PRISM construct surveys will be: - A practicing primary care provider at one of the participating sites or a TELESCOPE study navigator - Age 18 or older - Fluent in English Exclusion Criteria: For the cluster randomized trial, excluded will be patients who: - Do not speak English - Are not Hispanic or Latino(a) - Have a history of lung cancer - Had a CT scan in the past 12 months - Has been coughing up blood in the last two weeks - Have health conditions that make them poor candidates for curative treatment as determined by the primary care provider, - Are unable to provide informed consent Interviews Providers/administrators will be excluded if they: - Are unable to provide informed consent Online surveys - Are unable to provide informed consent - Women who are pregnant.
Please note that we have obtained the inclusion and exclusion criteria information from the National Institutes of Health’s clinical trials web site ClinicalTrials.gov. The listed criteria may not necessarily reflect recent amendments to the protocol and the current criteria.
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