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| Name | Class |
|---|---|
| National Cancer Institute (NCI) | NIH |
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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Videos | Experimental | Participants will be sent links to smoking cessation videos to watch. |
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| NCI Pamphlet | Active Comparator | Participants will be sent links to NCI's "Clearing the Air" to read. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Smoking cessation intervention | Other | Receive links to smoking cessation videos |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Acceptability | 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. | 1 week post-randomization |
| Feasibility | 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. | 1 week post-randomization |
| Retention Rates | We will determine if there are differences in retention rates between intervention groups. | 1 week, 1 month, and 3 months post-randomization |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in knowledge about quitting smoking | 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. | Baseline, 1 week, 1 month, and 3 months post-randomization |
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Inclusion Criteria:
Exclusion Criteria:
- Unstable or poorly managed medical or psychiatric conditions that impair cognition and ability to provide informed consent (e.g., dementia, active psychosis).
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Medical University of South Carolina | Charleston | South Carolina | 29425 | United States |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| ICF | No | No | Yes | Informed Consent Form | Jul 11, 2024 | Sep 10, 2025 | ICF_000.pdf |
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| ID | Term |
|---|---|
| D009369 | Neoplasms |
| D016540 | Smoking Cessation |
| ID | Term |
|---|---|
| D015438 | Health Behavior |
| D001519 | Behavior |
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| Informational intervention |
| Other |
Receive NCI's "Clearing the Air" booklet |
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| Changes in smoking behaviors | 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. | 1 week, 1 month, and 3 months post-randomization |