Actively Recruiting
Smoking Cessation Program in the Construction Sector
Led by University of Miami · Updated on 2025-09-03
608
Participants Needed
1
Research Sites
150 weeks
Total Duration
On this page
Sponsors
U
University of Miami
Lead Sponsor
F
Florida Department of Health
Collaborating Sponsor
AI-Summary
What this Trial Is About
The main objective of this study is to identify the optimal adaptive smoking cessation program for the construction sector in terms of effectiveness, cost-effectiveness, and potential implementation.
CONDITIONS
Official Title
Smoking Cessation Program in the Construction Sector
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Company leaders must be 18 years or older
- Company leaders involved in decision making
- Company leaders willing to participate in implementation development and evaluation
- Safety managers must be 18 years or older
- Safety managers must self-identify as a safety manager or superintendent
- Safety managers must have no plans to leave the company in the next year
- Safety managers must speak English or Spanish
- Safety managers must be non-cigarette smokers
- Safety managers willing to receive training in smoking cessation treatment
- Safety managers willing to deliver smoking cessation treatment to workers
- Construction workers must be employed as construction workers
- Construction workers must be 18 years or older
- Construction workers must have smoked on average 5 or more cigarettes daily for the past year
- Construction workers willing to make a serious quit attempt in the next 30 days
- Construction workers willing to receive treatment from the Florida Tobacco Quitline
- Construction workers planning to stay in the company for the next 6 months
- Construction workers must own a telephone and plan to keep it active for the next 12 months
You will not qualify if you...
- Safety managers who are current cigarette smokers
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Don Soffer Clinical Research Center
Miami, Florida, United States, 33136
Actively Recruiting
Research Team
T
Taghrid Asfar, MD
CONTACT
R
Roxana de Dios Despaux, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
6
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