A Novel Tobacco Cessation Resource for Smokers With a Diagnosed or Suspected Thoracic Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21+
SponsorOhio State University Comprehensive Cancer Center

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 volunteers

Qualifiers

>= 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

Design model

Single group

Treatments tested in this trial

  • Electronic Health Record Review

    Other intervention

    Ancillary studies

  • Informational Intervention

    Other intervention

    Receive smoking cessation information

  • Interview

    Other intervention

    Ancillary studies

  • Referral

    Other intervention

    Receive referral

  • Smoking Cessation Intervention

    Device

    Receive Buckeye Quit Stick

  • Survey Administration

    Other intervention

    Ancillary studies

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Prevention (Buckeye Quit Stick)Experimental treatment 6 interventions

Trial outcomes

Primary outcomes

1

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.

Time frame
Up to 1 year
2

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

Time frame
at baseline, 2 weeks, 3 months and 6 months
3

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.

Time frame
At 2 weeks, 3 months, and 6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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