Actively Recruiting
TELEhealth Shared Decision-making COaching for Lung Cancer Screening in Primary Care (TELESCOPE) for Hispanics
Led by Rutgers, The State University of New Jersey · Updated on 2025-12-02
91
Participants Needed
1
Research Sites
93 weeks
Total Duration
On this page
Sponsors
R
Rutgers, The State University of New Jersey
Lead Sponsor
N
New Jersey Commission on Cancer Research
Collaborating Sponsor
AI-Summary
What this Trial Is About
Aim 1: Culturally adapt the TELESCOPE intervention for Hispanics. Using iterative qualitative feedback from a study-specific Community Advisory Board, focus groups, and interviews with community members, the investigators will culturally adapt the TELESCOPE intervention for Hispanics at high risk for lung cancer. Aim 2: Assess the feasibility, acceptability, and implementation potential of the culturally adapted TELESCOPE intervention delivered by bilingual patient navigators for Hispanics. Hypothesis 1: The investigators expect a recruitment rate of ≥60%, ≥90% of Hispanic participants will complete the 1-week follow-up assessments, ≥80% of the key intervention components will be delivered with 80% fidelity by the patient navigators, and ≥90% of participants and clinicians will agree or completely agree that the intervention was feasible and acceptable. Aim 3: Explore the impact of a culturally adapted TELESCOPE intervention delivered by bilingual patient navigators vs enhanced usual care (EUC) on the initial uptake of low-dose computed tomography (LDCT) and quality of the shared decision-making (SDM) process. Hypothesis 2: The investigators expect that an adapted TELESCOPE intervention will result in higher uptake of LDCT and higher SDM quality for lung cancer screening (LCS) compared to EUC.
CONDITIONS
Official Title
TELEhealth Shared Decision-making COaching for Lung Cancer Screening in Primary Care (TELESCOPE) for Hispanics
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Identify as Hispanic or Latino(a)
- Able to read and speak English or Spanish
- Be between 50 and 77 years old
- Be a current or former smoker (quit within the past 15 years for aims 2-3)
- Have at least a 20 pack-year smoking history
- Scheduled for a non-acute care visit at a study site (for aims 2-3)
- Not coughing up blood in the last two weeks (for aims 2-3)
You will not qualify if you...
- 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
- Have been coughing up blood in the last two weeks
- Have health conditions making them poor candidates for curative treatment as determined by their primary care provider
- Unable to provide informed consent
- Women who are pregnant (for online surveys and provider participation)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Rutgers Cancer Institute
New Brunswick, New Jersey, United States, 08901
Actively Recruiting
Research Team
E
Evelyn Arana, DrPH
CONTACT
A
Arlette Chavez-Iniguez, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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