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Completed

NCT Number: NCT02276664

Capitalizing on a Teachable Moment to Promote Smoking Cessation

The purpose of this study is to develop and test a self-help smoking cessation treatment for patients receiving a lung cancer screening computed tomography (CT) scan.

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Key information

Conditions

Smoking Cessation Behavior Health Behavior

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

H Lee Moffitt Cancer Center

Tampa, Florida, 33612, United States

About this study

Conduct Formative Research (Months 1 - 4): Identification of emergent themes and responses to existing booklets.

Adapt and Refine Booklets (Months 5 - 8): Advanced drafts of booklets.

Final Reactions to Draft Booklets (Months 9 - 12): Series of smoking cessation booklets for spiral computed tomography (CT) patients.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Study 1

  • Participants for Study I will be drawn from a list of patients who have received a CT scan at the Moffitt Cancer Center
  • Smoked at least one cigarette per week prior to undergoing the CT scan
  • Able to speak and read English

Study 2

  • Smoked at least one cigarette over the past week
  • Able to read English

Treatment and study plan

Self-Help (SHI)

Behavioral

The newly revised Stop Smoking for Good booklets.

Usual care (UC)

Behavioral

The existing Clearing the Air smoking-cessation manual published by the National Cancer Institute (NCI).

Primary outcomes

  1. Study 1 - Completion of Formative Evaluation

    Time frame: Up to 12 months

    Complete formative research to adapt and refine the existing Stop Smoking for Good booklets.

  2. Study 2 - Rate of Seven-Day Abstinence

    Time frame: Seven-day abstinence will be assessed at each follow-up, allowing for calculation of point-prevalence abstinence rates. For this pilot, we will not bioverify self-reported abstinence.

    Up to 9 months

Secondary outcomes

  1. Rate of Intervention Demand

    Time frame: Up to 9 months

    Demand will be estimated by noting accrual rates into the study.

  2. Degree of Practicality

    Time frame: Up to 9 months

    Practicality encompasses the degree to which investigators are able to carry out all the piloted elements of the planned randomized control trial (RCT) successfully and efficiently (i.e., recruitment, screening, randomization, and follow-up).

Sponsors and collaborators

Lead sponsor

H. Lee Moffitt Cancer Center and Research Institute

Other

Collaborators

  • James and Esther King Biomedical Research Program

Registry information

Important dates

Study start
2014
Primary completion
2019
Study completion
2019
First posted
Oct 28, 2014
Registry last updated
Aug 13, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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