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The purpose of this study is to assess the efficacy of a novel telehealth-based intervention to reduce tobacco use among LGBTQ+ people.
Full 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.
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Interventional model
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30 participants in 2 patient groups
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Central trial contact
Mike Parent, PhD
Data sourced from clinicaltrials.gov
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