SmokefreeSGM, A Text-based Smoking Cessation Feasibility Trial for Sexual and Gender Minority Groups

Not Applicable

Completed

• Conditions: Smoking Cessation
• Interventions: Behavioral: SmokefreeSGM; Behavioral: SmokefreeTXT

• Registration Number: NCT05645354
• Lead Sponsor: The University of Texas Health Science Center, Houston

Brief Summary

The purpose of this study is to test the feasibility and acceptability of Smokefree Sexual and Gender Minority (SGM), an SGM-tailored version of the SmokefreeTXT text messaging program

Detailed Description

Not available

Study Timeline

• Study Start: 2022-11-10
• Study First Submitted: 2022-12-01
• Study First Submitted QC: 2022-12-01
• Study First Posted: 2022-12-09
• Status Verified: 2024-07
• Primary Completion: 2024-07-09
• Study Completion: 2024-07-09
• Last Update Submitted: 2024-07-10
• Last Update Posted: 2024-07-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

• Self-identify as an LGBTQ+ individual
• Currently live in Texas
• Have smoked at least 100 cigarettes in their lifetime, smoke every day, and smoke greater than or equal to 5 cigarettes a day
• Are willing to quit smoking in the next 15 days
• Have a cell phone number with an unlimited short message service (SMS) plan
• Have a positive cotinine saliva test to indicate their smoking status

Exclusion Criteria

• Have a prepaid cell phone plan (pay-as-you-go plan)
• Have a cell phone number that does not work and/or is registered to someone else
• Have inadequate equipment/devices (i.e., webcam, speakers, mic) for participating in telehealth sessions via Microsoft Teams, Webex, or Zoom AND cannot meet in-person
• Pregnant or breastfeeding persons (nicotine patches are not generally recommended to this groups since nicotine can affect fetal and neonatal brain development)
• Contraindication for nicotine patches. Absolute contraindications include: severe eczema or serious skin conditions, allergy to nicotine patches, pregnancy, breastfeeding, heart attack in the past 2 months, ongoing angina, peptic ulcer disease, arrhythmia, or uncontrolled blood pressure. Potential contraindications include: stroke in the past 6 months, insulin therapy, and a current diagnosis of liver, kidney, or heart disease. Study participants reporting a potential contraindication will require approval from their primary care provider and/or other treating physician (e.g., psychiatrist) to use nicotine patches. If the request is denied or not returned in 2 weeks, potential study participants will be excluded from the study.
• Current use of tobacco cessation medications
• Enrollment in another smoking cessation study
• Non-English speakers

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
SmokefreeSGM	SmokefreeSGM	-
SmokefreeTXT	SmokefreeTXT	-

Primary Outcome Measures

Name	Time	Method
Feasibility as assessed by number of participants that quit smoking	6 month follow up
Feasibility as assessed by number of participants that completed month 6 visit	end of month 6
Feasibility as assessed by number of participants recruited for the study	Baseline
Feasibility as assessed by number of participants that completed month 3 visit	end of month 3
Feasibility as assessed by number of participants that completed month 1 visit	end of month 1

Secondary Outcome Measures

Name	Time	Method
Acceptability as assessed by qualitative interviews	6 months follow up

Trial Locations

Locations (1)

The University of Texas Health Science Center at Houston; 🇺🇸 Houston, Texas, United States