About this trial
This clinical trial evaluates the feasibility of a novel tobacco cessation resource called a Buckeye Quit Stick among smokers with a diagnosed or suspected thoracic cancer. Tobacco use is the single most preventable cause of disease, disability, and death in the United States. While the benefits of quitting smoking are numerous, rates of persistent smoking after cancer diagnosis remain high. Research has found that patients who quit smoking but subsequently relapse frequently report the hand/oral habit as a barrier to sustained smoking cessation. The Buckeye Quit Stick is an innovative cessation aid designed to directly address patients' hand/oral habit by substituting the cessation aid for cigarettes without integrating pharmacologic intervention, which is typically managed by their medical provider and may require direct supervision due to the patient's health status. The Buckeye Quit Stick is designed to satisfy the repeated hand/oral pattern or ritual, thereby avoiding the physical loss of holding a cigarette in the hand or mouth and the action of smoking. It may also help occupy fidgeting hands and potentially reduce stress and cravings. This novel cessation resource may address key factors that influence smoking abstinence and improve patients' health outcomes.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
>= 21 years old
Speak and understand English
Established patient of the OSU thoracic clinics
Diagnosed with a thoracic malignancy or has a clinically suspected thoracic malignancy as documented by treating provider
Disqualifiers
< 21 years old (Ohio is a tobacco 21 state.)
Patient outside of the OSU clinics (This intervention targets patients who may benefit the most from cessation.)
Unwilling or unable to provide consent or complete study components
Prisoners will be excluded from participation
Trial design
Single group
Treatments tested in this trial
Electronic Health Record Review
Other interventionAncillary studies
Informational Intervention
Other interventionReceive smoking cessation information
Interview
Other interventionAncillary studies
Referral
Other interventionReceive referral
Smoking Cessation Intervention
DeviceReceive Buckeye Quit Stick
Survey Administration
Other interventionAncillary studies
Treatment groups
Trial outcomes
Primary outcomes
Recruitment rates (feasibility)
To evaluate feasibility, recruitment rates will be defined as the proportion of screened adults accrued relative to those approached in the Ohio State University Comprehensive Cancer Center thoracic oncology clinic.
Adherence (feasibility)
Adherence will be assessed by evaluating the proportion of retained participants at each timepoint who complete required study procedures and assessments at each timepoint
Retention rates (feasibility)
Retention rates will be defined as the percentage of participants not lost to follow-up at 2-weeks, 3-months and 6-months post-enrollment. Descriptive statistics will be performed.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.