MedTrace Logo

Nicotine Delivery Systems: Research & Treatment

NCT00108342 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2014-06-04

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to determine whether sampling nicotine replacement treatments (NRTs) is superior to learning about them by computer. Testing also covers preferences among the treatments. Subjects will be enrolled veterans who smoke.

Hypothesis: Direct experience ("sampling") of NRTs will increase knowledge about NRTs, motivation/confidence, use of NRTs and quit attempts in contrast to learning about NRTs by computer.

Conditions

  • Smoking

Interventions

DRUG

Nicotine gum - 2 mg and 4 mg

DRUG

Nicotine lozenges - 2 mg and 4 mg

DRUG

Nicotine inhaler (4 mg yield) - low and high "dosage" by frequency of puffing

can yield 4 mg from 10 mg device - infrequent and frequent puffing

OTHER

Computer learning

Sponsors & Collaborators

Principal Investigators

  • Nina G. Schneider, PhD · VA Greater Los Angeles Healthcare System, West LA

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-10-31
Primary Completion
2009-09-30
Completion
2009-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00108342 on ClinicalTrials.gov