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
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | contingency management | Prize-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. |
| OTHER | Standard of Care | varenicline (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. |
| OTHER | Standard of Care | Twice 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.