Medical University of South Carolina
Charleston, South Carolina, 29425, United States
NCT Number: NCT06307496
The purpose of the current study is to pilot the efficacy, feasibility, and acceptability of an evidence-based smoking cessation intervention adapted for cancer patients and delivered via video. Investigators aim to assess if this intervention is considered acceptable by participants, feasible to implement, and effective at increasing knowledge about smoking cessation before conducting a fully powered clinical trial.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Charleston, South Carolina, 29425, United States
A randomized controlled pilot study is being conducted to test the acceptability and feasibility of a smoking cessation intervention tailored for cancer patients that is delivered via video. Participants will be in a video intervention or control group that receives information about quitting smoking. Participants will complete surveys prior to randomization, and will complete additional surveys one week, one month, and three months post-randomization to provide their thoughts about the videos, information about changes to smoking behaviors, and knowledge about quitting smoking.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Receive links to smoking cessation videos
Receive NCI's "Clearing the Air" booklet
Time frame: 1 week post-randomization
Acceptability will be measured using the Acceptability of Intervention measure, which contains four items with answer options on a scale from 1-5, with higher scores indicating higher acceptability. We will consider the intervention "acceptable" if an average score of 4 or higher is obtained.
Time frame: 1 week post-randomization
Feasibility will be measured using the Feasibility of Intervention measure, which contains four items with answer options on a scale from 1-5, with higher scores indicating higher feasibility. We will consider the intervention "feasible" if an average score of 4 or higher is obtained.
Time frame: 1 week, 1 month, and 3 months post-randomization
We will determine if there are differences in retention rates between intervention groups.
Time frame: Baseline, 1 week, 1 month, and 3 months post-randomization
We will assess changes in knowledge about tools to quit smoking and the role of nicotine, etc. from prior to randomization (before the intervention is delivered) to post-randomization follow-ups. These questions will be generated by the study investigators based on video content.
Time frame: 1 week, 1 month, and 3 months post-randomization
We will assess the number of 24-hour quit attempts and 7-day point prevalence at 1 week, 1 month, and 3 month follow-ups.
Medical University of South Carolina
Other
Video Interventions for Dependence On Smoking (VIDeOS) for Cancer Patients: A Randomized Controlled Pilot Study
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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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