TinCat LGBTQ+ Smoking Cessation Via Asynchronous Telehealth
- Conditions
- Tobacco Use CessationTobacco Use Disorder
- Registration Number
- NCT05499364
- Lead Sponsor
- University of Texas at Austin
- Brief Summary
The purpose of this study is to assess the efficacy of a novel telehealth-based intervention to reduce tobacco use among LGBTQ+ people.
- Detailed Description
After being informed about potential risks and screened into the study, patients will be randomized into the treatment or control group. Control group participants will complete 7 sessions based on quit.gov smoking cessation planning. Intervention participants will complete 7 sessions of individualized asynchronous telehealth sessions.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 30
- Age 18 and over
- Live in Greater Austin
- Identify as LGBTQ+
- Current smokers
- High speed internet access
- Exceed screener cutoff for suicide risk
- Exceed screener cutoff for borderline personality disorder
- Report current active substance use other than tobacco that interferes with functioning
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Tobacco use 11 weeks Cigarette and vape assessments based on prior research on vaping/smoking:
Cigarette: Today, did you have at least one puff on a cigarette (yes/no) IF YES, THEN How many cigarettes did you smoked (at least one puff) (1-"more than 60").
Vaping: Today, did you use an electronic nicotine delivery system (i.e., a vape containing nicotine), even just one puff? (yes/no) IF YES, THEN How many times they had at least one puff (1 time, 2-5 times, 6-10 times, 11-15 times, 16-20 times, 21-25 times, 26-30 times, 31 or more times).
- Secondary Outcome Measures
Name Time Method