Actively Recruiting
Implementation of Tobacco Cessation Programming at Community Behavioral Health Sites
Led by University of Chicago · Updated on 2026-04-14
24
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
Sponsors
U
University of Chicago
Lead Sponsor
R
Respiratory Health Association
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Implementation of Tobacco Cessation Programming at Community Behavioral Health Sites
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Identify as someone who currently smokes combustible cigarettes daily (at least 1 cigarette per day) for the past month
- Report interest in quitting smoking (at least 6 out of 10 on interest scale)
- Age 18 or older
- Ability to understand English
- Willing and able to provide informed consent
- Have a stable residence and contact information throughout the follow-up period
You will not qualify if you...
- Use cigarettes non-daily or intermittently
- No interest in quitting smoking
- Unstable residence or not staying in Chicago during study period
- Current untreated severe substance use disorder (except tobacco)
- Past-year serious untreated psychiatric illness such as schizophrenia, bipolar disorder, obsessive compulsive disorder, unspecified psychosis, or past-year suicide attempt
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Chicago
Chicago, Illinois, United States, 60637
Actively Recruiting
Research Team
E
Emma Brett, PhD
CONTACT
S
Sophie Miller, BS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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