Evaluating the Impact of CONNECT in a Multilingual Population
University of California, San Francisco · with Tobacco Related Disease Research Program · NCT07111936
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 50–80 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 439
- US sites recruiting
- 1
- Study start
- August 7, 2025
- Record last updated
- August 13, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study aims to broaden the reach of the lung cancer screening (LCS) CONNECT program (NCT04149249, NCT06213532), by developing a version of the program to be available to multilingual communities. The CONNECT program encourages individuals who are undergoing lung cancer screening to also quit smoking by providing a personalized program which includes a video doctor with personalized responses, text message and telephone call support and connection with a pharmacist to assist in obtaining nicotine replacement medication. This clinical trial will develop and ultimately test how well the CONNECT Multilingual (CONNECT ML) program works to improve smoking cessation among current adult smokers within the Spanish and Cantonese speaking communities.
Being studied: CONNECT Intervention for multilingual populations; Saliva Sample; Interview
Conditions: Smoking Cessation; Smoking Cessation Counseling Ability and Practice; Smoking Cessation Counselling; Lung Cancer Screening
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Age 50-80 years old.
- Current smokers defined at smoking at least one cigarette in past 7 days AND eligible for lung cancer screening (LCS) based on smoking history (>=20 pack year history)
- California (CA) residents
- Able to understand and comply with study procedures for the entire length of the study.
- Ability of individual or legal guardian/representative to understand a written informed consent document, and the willingness to sign it.
Exclusion Criteria
- Non-smokers.
- Individuals with a diagnosis of lung cancer.
- Individuals receiving hospice care.
- Individuals whose providers do not think that they should participate (e.g., psychiatric illness or significant cognitive impairment that would impede the individuals ability to participate).
- Hearing and/or vision disabilities that would prevent participants from adequately receiving treatment components such as video or telephone counseling.
Recruiting US locations
University of California San Francisco
San Francisco, CA 94143
Site contact: Anita Ponce, MSc · 415-502-1317 · Anita.Ponce@ucsf.edu
Study contacts (from the official record)
- Anita Ponce, MSc · 415-502-1317 · Anita.Ponce@ucsf.edu
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