Viewing Study NCT06637358



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06637358
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-10-09

Brief Title: A Text-based Reduction Intervention for Smokeless Tobacco Cessation- Pilot Study
Sponsor: None
Organization: None

Study Overview

Official Title: A Text-based Reduction Intervention for Smokeless Tobacco Cessation- Pilot Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: All participants will receive the EnufSnuffTXT 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 EnufSnuffTXT intervention or into receiving an additional 8-10 weeks of the EnufSnuffTXT intervention along with a dedicated text quit coach to send and receive live support
Detailed Description: All participants will receive the EnufSnuffTXT 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 EnufSnuffTXT intervention or into receiving an additional 8-10 weeks of the EnufSnuffTXT 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 6-month follow-up after intervention completion The investigators will also conduct a brief midpoint check in between end of program and 6-month follow-up assessment with participants to ask if they have quit using smokeless tobacco Research staff will email participants redcap surveys at baseline end of program midpoint check in and 6-months Participants will be able to opt for a recorded telephone interview at EOP 12-week and 6-month Each opted-in participant will be interviewed only once ie if a participant is interviewed at 12- week they will not be interviewed at 6-month

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None