Actively Recruiting
Developing a Scalable Tobacco Cessation Program for Cancer Survivors and Caregivers
Led by University of Florida · Updated on 2025-07-16
204
Participants Needed
1
Research Sites
68 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Given the challenges to delivering tobacco cessation treatment in oncology care and the unique challenges faced by individuals attempting to quit tobacco after a cancer diagnosis, scalable cessation programs that are tailored to the experiences of cancer survivors that also integrate caregiver/family support are needed. To address this need, this study will use an intervention that consists of two primary strategies: 1) a tailored cessation program for cancer survivors and family members/caregivers who use tobacco and 2) healthcare provider training. Healthcare providers will receive training on the AAC model (Ask patients about tobacco use, Advise patients to quit, Connect patients to cessation resources), including materials focused on tobacco cessation in cancer care from the CDC, as well as a brief evidence-based communication skills training based on the C-LEAR (Counsel, Listen, Empathize, Answer, Recommend) approach.
CONDITIONS
Official Title
Developing a Scalable Tobacco Cessation Program for Cancer Survivors and Caregivers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- Current self-reported user of any tobacco or nicotine product in the past month (e.g., cigarettes, e-cigarettes, cigars, dip/chew)
- History of cancer diagnosis or currently receiving cancer-related treatments (for cancer survivors)
- Receiving care from participating UF Health clinics (Medical Oncology, Urology, Radiation Oncology)
- Capable of completing study requirements
- Provided informed consent and agreement to comply with study processes
- Family members, informal caregivers, or friends of enrolled cancer survivors receiving care at participating UF Health clinics (for caregivers/family members)
You will not qualify if you...
- Unable to complete sessions due to language, travel, or technology barriers
- Prisoners or involuntarily incarcerated individuals
- Individuals compulsorily detained for treatment of psychiatric or physical illness
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Florida
Gainesville, Florida, United States, 32608
Actively Recruiting
Research Team
E
Erika Barahona, M. Ed
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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