Clinical Trials Directory

Trials / Completed

CompletedNCT00683280

Contingency Management and Pharmacotherapy for Smoking Cessation

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
59 (actual)
Sponsor
UConn Health · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In total, 70 smokers will be randomized to: standard of care smoking cessation medication varenicline alone (an FDA-approved smoking cessation medication) or varenicline plus contingency management (CM) (a behavioral procedure with rewards for target behaviors, like smoking abstinence). Patients in both conditions will receive varenicline for 12 weeks with standard smoking cessation therapy and regular breath and urine sample monitoring for smoking. Patients assigned to CM will earn chances to win prizes for each breath sample that tests negative for smoking, and urine samples that test negative for smoking will result in even greater chances for prizes. More CM patients are expected to achieve and maintain abstinence than patients receiving varenicline alone.

Conditions

Interventions

TypeNameDescription
BEHAVIORALcontingency managementPrize-based contingency management, with the opportunity to earn prizes for expired carbon monoxide levels reading 6ppm or less and urinary cotinine levels reading 30ng/ml or less for 4 weeks.
OTHERStandard of Carevarenicline (smoking cessation medication) 0.5mg po daily Days 1-3, 0.5mg po twice daily Days 4-7, 1.0 mg po twice daily Days 8-84.
OTHERStandard of CareTwice weekly brief counseling based on public health service guidelines for quitting smoking.

Timeline

Start date
2008-05-01
Primary completion
2010-08-01
Completion
2010-08-01
First posted
2008-05-23
Last updated
2018-01-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00683280. Inclusion in this directory is not an endorsement.