Summary

Eligibility
for people ages 50-80 (full criteria)
Healthy Volunteers
healthy people welcome
Location
at San Francisco, California
Dates
study started
study ends around
Principal Investigator
by Judith Walsh, MD, MPH

Description

Summary

This study aims to broaden the reach of CONNECT, a program designed to encourage people who are having a lung cancer screening test to also quit smoking. CONNECT targets smokers who are undergoing lung cancer screening and includes an interactive Video Doctor which provides participants with information tailored to their individual responses as well as proactive outreach using brief telephone calls and text messaging to follow up and connect smokers with evidence-based resources for smoking cessation.

This study will develop versions in Spanish and Cantonese of CONNECT, and will offer additional proactive outreach and streamlined access to nicotine replacement therapy (NRT) including direct pharmacist furnishing. We will evaluate the impact of the revised CONNECT on smoking cessation outcomes.

Official Title

Evaluating the Impact of CONNECT, a Novel Smoking Cessation Intervention, in a Diverse, Multi-lingual Population

Details

In the first phase of the study, we will conduct focus groups and beta testing with English, Spanish and Cantonese speaking participants which will inform the cultural adaptation, fine tuning and updating of the CONNECT smoking cessation intervention.

In a randomized controlled trial, we will assess the impact of CONNECT on the outcomes of rates of smoking cessation at 6 months, cotinine verified 7-day smoking cessation and utilization of smoking cessation resources and pharmacotherapy in a diverse group of English, Spanish, and Cantonese speaking high-risk smokers who will be randomized to 1 of of 2 groups.

Group 1: Participants receive the CONNECT Multi-lingual intervention. The intervention consists of two components 1) multilingual CONNECT Video Doctor; and 2) Proactive Outreach.

Group 2: Participants receive usual care from their primary care provider.

Group 1 and 2 participants are followed up at 1-week, and 1, 3, and 6 months. At 6-months, participants will be asked to complete an at-home saliva kit to verify their smoking status.

Keywords

Smoking Cessation, Smoking Cessation Counseling Ability and Practice, Smoking Cessation Counselling, Lung Cancer Screening, CONNECT Intervention

Eligibility

You can join if…

Open to people ages 50-80

  • Age 50-80
  • Male or female
  • Current smokers (at least one cigarette in past 7 days) AND eligible for lung cancer screening (LCS) by smoking history (≥20 pack year history and current smokers)
  • CA residents
  • Able to understand study procedures and to comply with them 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.

You CAN'T join if...

  • 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., those with psychiatric illness or significant cognitive impairment).
  • Have hearing and/or vision disabilities in receiving treatment components such as video or telephone counseling.

Location

  • UCSF
    San Francisco California 94143 United States

Lead Scientist at UCSF

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT07111936
Study Type
Interventional
Participants
Expecting 439 study participants
Last Updated