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临床试验/NCT06307496
NCT06307496已完成不适用

Video Interventions for Dependence On Smoking (VIDeOS) for Cancer Patients: A Randomized Controlled Pilot Study

Medical University of South Carolina2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2024年9月24日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
2
主要终点
Feasibility

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 or older
  • Diagnosed with cancer (any type)
  • Receiving care at Medical University of South Carolina
  • Reads and understands English language
  • Currently smoking cigarettes (any amount)

排除标准

  • - Unstable or poorly managed medical or psychiatric conditions that impair cognition and ability to provide informed consent (e.g., dementia, active psychosis).

结局指标

主要结局

Feasibility

时间窗: 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.

Retention Rates

时间窗: 1 week, 1 month, and 3 months post-randomization

We will determine if there are differences in retention rates between intervention groups.

Acceptability

时间窗: 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.

次要结局

  • Changes in smoking behaviors(1 week, 1 month, and 3 months post-randomization)
  • Changes in knowledge about quitting smoking(Baseline, 1 week, 1 month, and 3 months post-randomization)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kinsey Pebley

Post Doctoral-Fellow

Medical University of South Carolina

研究点 (2)

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