Smokeless Tobacco Cessation Intervention for Firefighters
Development of a M-Health Smokeless Tobacco Cessation Intervention for Firefighters
2 other identifiers
interventional
60
1 country
1
Brief Summary
The investigators are asking professional firefighters across North Carolina to take part in focus groups to discuss the specific needs of firefighters in smokeless tobacco cessation. About 40 firefighters will take part in the focus groups. The purpose of the focus groups is to learn how firefighting and shift work impact smokeless tobacco use and risk perceptions related to chew or dip. Using their feedback, the study team will then develop a cessation program specifically geared towards firefighters and first responders. The cessation program will be a mobile text / chat intervention specifically tailored to needs of firefighters and first responders who wish to stop using smokeless tobacco. About 50 firefighters and first responders will take part in this program, while being randomized into either the intervention group or the control group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2022
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 1, 2021
CompletedFirst Posted
Study publicly available on registry
November 8, 2021
CompletedStudy Start
First participant enrolled
January 25, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 10, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 10, 2024
CompletedResults Posted
Study results publicly available
December 13, 2024
CompletedDecember 13, 2024
November 1, 2024
2 years
November 1, 2021
November 20, 2024
November 20, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (8)
Number of First Responders Recruited Who Completed a Screening Assessment
Within 3 months of the initiation of study recruitment
First Responders Who Met the Study Eligibility Criteria, Were Enrolled, and Randomized to a Treatment Arm
Within 3 months of the initiation of study recruitment
Percent of Participants Engaged With the Program as Measured by Completion of the End of Program Questionnaire
Study engagement defined as completing the End of Intervention Program assessment.
30 days following the end of the 10-week intervention
Number of Participants Who Stated Intervention Was Useful as Measured by Questionnaire
Usefulness was measured on a scale of 1-5, where 1=Not at all useful, 2=Somewhat useful, 3=Undecided, 4=Very useful, 5=Extremely useful. Ratings were dichotomized for the analysis as 0=no (not at all, somewhat, undecided) or 1=yes (very, extremely useful).
30 days following the end of the 10-week intervention
Number of Participants Who Stated That #EnufSnuff.TXT Intervention Was Helpful as Measured by Questionnaire
Helpfulness was measured on a scale of 1-5 where 1=not at all, 2=somewhat, 3=Undecided, 4=very, 5=extremely. Ratings were dichotomized for the analysis as 0=no (not at all, somewhat, undecided) and 1=yes (very, extremely).
30 days following the end of the 10-week intervention
Number of Participants Who Stated Intervention Made Them Consider Quitting as Measured by Questionnaire
Considered quitting was measured on a scale of 1-5, where 1=Not at all useful, 2=Somewhat useful, 3=Undecided, 4=Very useful, 5=Extremely useful. Ratings were dichotomized for the analysis as 0=no (not at all, somewhat, undecided) or 1=yes (very, extremely useful).
30 days following the end of the 10-week intervention
Number of Participants Who Stated They Would Recommend Program to a Friend as Measured by Questionnaire
Recommend to friend was measured on a scale of 1-5, where 1=Not at all useful, 2=Somewhat useful, 3=Undecided, 4=Very useful, 5=Extremely useful. Ratings were then dichotomized for the analysis as 0=no (not at all, somewhat, undecided) or 1=yes (very, extremely useful).
30 days following the end of the 10-week intervention
Number of Participants Who Quit Smokeless Tobacco Measured by Self Report
Quit was determined by the self-report response (yes or no) to the question, "In the past 7 days, have you used any dip?"
30 days following the end of the 10-week intervention
Study Arms (2)
#EnufSnuff.TXT- First Responder
EXPERIMENTALParticipants in this group will receive a mobile gradual smokeless tobacco reduction intervention
Enough Snuff Intervention
ACTIVE COMPARATORParticipants in this group will receive tobacco cessation materials
Interventions
Participants in this intervention will be given the choice of following the Gradual Reduction to Quit program or to choose their own quit date within 2-4 weeks. The Gradual Reduction to Quit program will reduce smokeless tobacco use via text message support and weekly prompts guiding the participants to gradually decrease their use of smokeless tobacco until they are down to zero. A four week Nicotine Replacement Therapy (NRT) sample in the form of lozenges will also be provided to all participants. The intent of this program is to reduce the number of times participants use smokeless tobacco.
Participants will be sent the Enuf Snuff cessation manual, support text messages, as well as a four week Nicotine Replacement Therapy (NRT) sample in the form of lozenges.
Eligibility Criteria
You may qualify if:
- Professional firefighters or first responders
- years or older
- Have used smokeless tobacco for the past year and current (past 30 days) smokeless tobacco daily use
- Access to a smartphone
You may not qualify if:
- Not a professional firefighter or first responder
- Under 18 years of age
- Have not used smokeless tobacco for the past year and are not current (past 30 days) smokeless tobacco daily use
- No access to a smartphone
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Duke Universitylead
- National Cancer Institute (NCI)collaborator
Study Sites (1)
Duke University
Durham, North Carolina, 27705, United States
Related Publications (1)
Noonan D, Fish LJ, Silva SG, Da Costa M, Simmons LA, Garcia Ortiz N, Swinkels C, Jung D, Severson HH, Pollak KI. #EnufSnuff.TXT-FirstResponder: a pilot randomized controlled trial of a text message intervention for smokeless tobacco cessation among First Responders. Front Public Health. 2026 Jan 19;13:1699800. doi: 10.3389/fpubh.2025.1699800. eCollection 2025.
PMID: 41635441DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Devon Noonan, Ph.D.
- Organization
- Duke University
Study Officials
- PRINCIPAL INVESTIGATOR
Devon Noonan, PhD
Duke University
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 1, 2021
First Posted
November 8, 2021
Study Start
January 25, 2022
Primary Completion
January 10, 2024
Study Completion
January 10, 2024
Last Updated
December 13, 2024
Results First Posted
December 13, 2024
Record last verified: 2024-11
Data Sharing
- IPD Sharing
- Will not share