Tailored Smoking Cessation Intervention in Promoting Sexual and Gender Minority Smokers to Quit Smoking

Completed · Not applicable

Conditions studied: Cigarette Smoker, Current Every Day Smoker

In brief

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.

Key facts

Study ID

NCT03669120

Run by

M.D. Anderson Cancer Center

People needed

46

Starts

2018-08-10

Expected to finish

2020-03-25

Last updated by the study team

2020-04-02

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• M D Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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