University of Chicago
The goal of this study is to: partner with Respiratory Health Association and determine barriers and unmet smoking cessation treatment needs from leaders in behavioral health organizations, treatment programs and adults who smoke (AWS) in Chicago. This will be accomplished by establishing a community advisory board (CAB) and pilot testing a community-informed smoking cessation treatment within a community behavioral health organization to determine its feasibility after addressing implementation issues.
Nicotine Use Disorder
Smoking Cessation
Smoking Cessation Intervention
Enhanced Courage to Quit
NA
The purpose of the proposed study is to determine barriers and unmet smoking cessation treatment needs from leaders in behavioral health organizations, behavioral health treatment providers, and community members in Chicago and pilot test a community-informed, targeted rolling smoking cessation treatment within a community organization. The research team and the Respiratory Health Association (RHA) will work together to identify community sites that could derive possible benefit from adopting and implementing the targeted treatment. Aim 1: Develop a Community Advisory Board (CAB) comprised of providers, community members, and organization leadership. Aim 2: Use a mixed-methods approach to understand barriers, facilitators, and unmet treatment needs regarding smoking cessation treatment within the community. Aim 3: Pilot test the targeted smoking cessation treatment across a 3-month period at one community site through partnership with Respiratory Health Association. Hypothesis: The targeted intervention will demonstrate feasibility and acceptability.
Study Type : | INTERVENTIONAL |
Estimated Enrollment : | 24 participants |
Masking : | NONE |
Primary Purpose : | TREATMENT |
Official Title : | Enhancing the Implementation of Tobacco Treatment: A Community-responsive Approach |
Actual Study Start Date : | 2025-07 |
Estimated Primary Completion Date : | 2026-07 |
Estimated Study Completion Date : | 2027-01 |
Information not available for Arms and Intervention/treatment
Ages Eligible for Study: | 18 Years |
Sexes Eligible for Study: | ALL |
Accepts Healthy Volunteers: |
Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.
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