SmokefreeSGM, A Text-based Smoking Cessation Intervention for Sexual and Gender Minority Groups
- Conditions
- Smoking Cessation
- Interventions
- Behavioral: SmokefreeSGM
- Registration Number
- NCT05029362
- Brief Summary
The purpose of this study is to pretest the design of a text-based smoking cessation program tailored to sexual minority individuals.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 18
- Smoke five or more cigarettes per day, has smoked at least 100 cigarettes in their lifetime and smokes everyday
- Have an interest in quitting smoking in the next 15 days
- Have a cellphone number with an unlimited short messaging service (SMS) plan
- Have US mailing and email addresses
- Positive cotinine saliva test results
- Individuals who are found to have a prepaid cell phone
- Individuals who are found to have a cellphone number that does not work or is registered to someone else
- Pregnant or breastfeeding women
- Contraindication for nicotine patch
- Regular use of tobacco products other than cigarettes
- Current use of tobacco cessation medications
- Enrolled in another smoking cessation study
- Non-English speakers
- Having inadequate equipment/device (webcam, speakers, mic) for participating in telehealth sessions
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Beta testing group SmokefreeSGM -
- Primary Outcome Measures
Name Time Method Perceived Usability as Assessed by the System Usability Scale (SUS) 1 month after quit date The 10-item System Usability Scale (SUS) was used to assess the usability of the SmokefreeSGM text messaging program. Total score ranges from 0 to 100, with a higher score indicating greater acceptability and a score above 75 indicating that the program is perceived as acceptable.
- Secondary Outcome Measures
Name Time Method Engagement as Assessed by the Number of Text Messages Sent and Received by Study Participants After Enrollment. 1 month after enrollment A participant's engagement rate was determined by dividing the total number of participant responses to the bidirectional text messages (numerator) by the total number of bidirectional text messages sent by the text-based platform (denominator). Participants who had rates ≤33.3% were classified as having low engagement, 33.3-66.6% moderate engagement, and ≥66.7% high engagement. Data are reported categorically as number of participants who have low, moderate, or high engagement.
Trial Locations
- Locations (1)
The University of Texas Health Science Center at Houston
🇺🇸Houston, Texas, United States