Evaluating a Tobacco Harm Reduction Strategy Among Clients Enrolled in Substance Use Disorder Treatment

Sponsor:
NIH/NIDA
Sponsor Study ID:
R01DA059969
CTO #:
104065
NCT Number:
NCT06922617
Phase:
N/A
Protocol Type:
Prevention
Age Group:
Adults
Disease Sites:
Study Objectives:
Evaluate if switching to ENDS leads to greater rates of 7-day biologically confirmed point prevalence abstinence (PPA) from cigarette smoking at 12 weeks compared to quitting with NRT among those enrolled in SUD treatment. Evaluate patient, provider, and organizational-level implementation outcomes using mixed methods according to the Proctor framework. Outcomes include: acceptability, appropriateness and feasibility. Quantitative data will be supplemented with in-depth interviews with patients (n=25), providers (n=10), and organizational stakeholders (n=6) to identify barriers and facilitators to implementation
eConsent:
Not available
Study Documents:
Open Study Documents
(MUSC NetID required for document access)

For more information about this trial please contact the study team:

  • Medical University of South Carolina

Trial opened at the following institutions:

Shoreline Behavioral Health, Medical University of South Carolina, Behavioral Health Services of Pickens County