Clinical Alternatives for Reducing Harm Using E-cigarettes
NCT07039292 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 208
Last updated 2026-05-08
Summary
For patients in cancer care, quitting smoking is critical, but a significant portion of patients in cancer care refuse all components of tobacco treatment, even when offered free of charge. The proposed clinical trial will assess one harm reduction intervention, switching completely from cigarettes to e-cigarettes, among oncology outpatients who smoke and refuse traditional tobacco treatment. This study is a type 1 hybrid effectiveness-implementation trial among oncology outpatients at an NCI-designated cancer center who smoke and refuse all components of tobacco treatment (N=208).
Conditions
- Smoking
- E-Cig Use
- Oncology
Interventions
- BEHAVIORAL
-
Harm Reduction (E-cigarette switching)
Participants will be assigned to receive an e-cigarette and try to switch completely from smoking to using the e-cigarette
- BEHAVIORAL
-
Standard of Care
Participants will be assigned to receive tobacco treatment referrals and the opportunity to re-enroll in the Tobacco Treatment Program
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH -
National Institutes of Health (NIH)
collaborator NIH -
Medical University of South Carolina
lead OTHER
Principal Investigators
-
Alana Rojewski · Medical University of South Carolina
-
Tracy Smith · Medical University of South Carolina
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-08-25
- Primary Completion
- 2029-05-31
- Completion
- 2029-11-30
Countries
- United States
Study Locations
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