Tailored or Non-Tailored Smoking Cessation Intervention for Sexual and Gender Minorities
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 46
- 试验地点
- 2
- 主要终点
- Retention rates
研究概览
简要总结
This trial studies how well tailored smoking cessation intervention works in promoting sexual and gender minority smokers to quit smoking. A program that is specifically designed for the lesbian, gay, bisexual, and transgender community may affect these participants differently than a traditional approach.
详细描述
PRIMARY OBJECTIVES:
I. To test the feasibility of two different approaches for smoking cessation (print materials developed for smoking cessation among the mainstream population versus [vs.] an individualized text based approach) among 60 lesbian, gay, bisexual, and transgender (LGBT) smokers.
SECONDARY OBJECTIVES:
I. To assess the levels of helpfulness, appropriateness, and perceived difficulty of the above mentioned cessation approaches among 60 LGBT smokers.
EXPLORATORY OBJECTIVES:
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Male or female owning a cell phone with a reachable contact number
- •Self-identified as LGBT individual, regardless human immunodeficiency virus (HIV) serologic status
- •Smoked at least 100 cigarettes in lifetime
- •Currently smoking at least 5 cigarettes a day, on average
- •Willing to set a quit smoking date within a week of the enrollment
- •English speaking
排除标准
- •Expired carbon monoxide (CO) levels below 7 ppm
- •Positive history of a medical condition that precludes use of the nicotine patch (e.g., recent myocardial infarction, significant skin disorder, previous severe adverse reaction to nicotine patch, pregnant or breast feeding, assessed with our standard protocol for determining NRT eligibility)
- •Current use of NRT or other smoking cessation medications (e.g., varenicline or bupropion)
- •Pregnant or nursing
- •Enrolled in another smoking cessation program
- •Partner enrolled on current study
结局指标
主要结局
Retention rates
时间窗: At 3 and 6 months
Will be summarized using descriptive statistics such as the mean, standard deviation, median, interquartile range, and frequency where appropriate. Confidence intervals of 90% for the participating rates at baseline and retention rates at 3- and 6- follow-up will be provided.
Computing recruitment rate
时间窗: At baseline
Will be summarized using descriptive statistics such as the mean, standard deviation, median, interquartile range, and frequency where appropriate. Confidence intervals of 90% for the participating rates at baseline and retention rates at 3- and 6- follow-up will be provided.
次要结局
- Levels of helpfulness(Up to 6 months)
- Appropriateness(Up to 6 months)
- Perceived difficulty(Up to 6 months)