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Electronic Cigarettes (E-cigarettes) as a Harm Reduction Strategy

Smoking Clinical Trial

Official title:
Assessing the Use of Electronic Cigarettes (E-cigarettes) as a Harm Reduction Strategy

Clinical Trial Summary

The purpose of this study is to examine the feasibility of using e-cigarettes as a method for harm reduction and the effects of providing e-cigarettes (or placebo e-cigarettes) on smoking outcomes. Participants will be randomized to receive either e-cigarettes with nicotine cartridges or e-cigarettes with placebo cartridges, and followed for 3 weeks.

Clinical Trial Description

This pilot study will be a two-arm, randomized controlled trial. The investigator will randomize 40 participants into each intervention arm. Participants will be randomized to one of the two arms: e-cigarettes with nicotine cartridges or e-cigarettes with placebo cartridges (0mg). Participants and research assistants will be blind to the allocation of nicotine or placebo e-cigarettes as there are no difference in appearance or odor of the mist emitted from the e-cigarettes with and without nicotine containing cartridges. Participants will be asked to track their nicotine use via text message. All participants will receive a 20-30 minute behavioral counseling consultation with a trained tobacco counselor. Counselors will review each participant's smoking pattern and offer tailored behavioral and environmental change strategies including specific smoking reduction strategy options. Participants will be given a supply of e-cigarettes and followed for 3 weeks ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02628964
Study type Interventional
Source NYU Langone Health
Contact
Status Completed
Phase N/A
Start date May 2015
Completion date March 26, 2018
View Details
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