A Text-based Reduction Intervention for Smokeless Tobacco Cessation- Pilot Study
- Conditions
- Smokeless Tobacco Cessation
- Registration Number
- NCT06637358
- Lead Sponsor
- Duke University
- Brief Summary
All participants will receive the EnufSnuff.TXT scheduled gradual reduction (SGR) intervention for 6 weeks and, for those who do not reach the point of quit, includes getting randomized (like the flip of a coin) into either an additional 8-10 weeks of the EnufSnuff.TXT intervention or into receiving an additional 8-10 weeks of the EnufSnuff.TXT intervention along with a dedicated text quit coach to send and receive live support.
- Detailed Description
All participants will receive the EnufSnuff.TXT intervention (a text-based personalized reduction plan and daily text-based cessation support messages) for 6 weeks and, for those who report that they have not achieved complete cessation, includes getting randomized into either an additional 8-10 weeks of the EnufSnuff.TXT intervention or into receiving an additional 8-10 weeks of the EnufSnuff.TXT intervention along with a dedicated quit coach to send and receive live text support. The investigators will conduct phone-based or smart phone-based assessments with participants at baseline, end of program, and 7-month follow-up after intervention completion. The investigators will also conduct a brief midpoint check (after the first 6 weeks of intervention) with participants to ask if they have quit using smokeless tobacco. Research staff will email participants redcap surveys at baseline, end of program, and 7-months. Participants will be able to opt for a recorded telephone interview at the 7-month check-in. Each opted-in participant will be interviewed only once.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 69
- 18 years of age and older
- Have used smokeless tobacco for the last year, currently dip 3 or more times a day
- Have an address in a rural census tract defined by a RUCC code of 4-10 and/or an IMU of 62 or lower
- Interested in participating in a cessation program; and
- Have access to a cell phone with unlimited texting ability.
- Non-English speaking;
- Have smoked cigarettes or used any other tobacco product in the past 30 days (i.e., dual user) and are not willing to abstain during the intervention period
- Currently participating in a smokeless tobacco cessation study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Feasibility as measured by the number of recruited individuals who enrolled Baseline Feasibility as measured by the number of participants who left the study (attrition) Up to 6 months Acceptability as measured by the number of participants who found the intervention useful Up to 6 months As measured via telephone interview.
Acceptability as measured by the number of participants who reported that the intervention received changed their smokeless tobacco use Up to 6 months As measured via telephone interview.
Acceptability as measured by the number of participants who reported that the intervention made them think about quitting Up to 6 months As measured via telephone interview.
Acceptability as measured by the number of participants who reported that they would recommend the program to a friend Up to 6 months As measured via telephone interview.
Preliminary efficacy as measured by the number of participants who quit smokeless tobacco by the end of treatment Up to approximately 16 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Duke University
🇺🇸Durham, North Carolina, United States