N/A
Completed N=103
Low-Cost Contingency Management for Smoking Cessation
Tobacco Use Cessation
Source: ClinicalTrials.gov NCT01040260 ↗
Enrolled (actual)
103
Serious AEs
0.0%
Results posted
Aug 2013
Primary outcomePrimary: Abstinence Rate — 8; 10 participants
Summary
An innovative low-cost form of contingency management has been developed in which participants receive the chance to draw vouchers from a fish bowl depending on whether or not their abstinence from tobacco is confirmed by expired-air carbon monoxide. The vouchers can be redeemed for prizes of varying value. This form of contingency management has been shown to be effective in the treatment of a variety of substance use disorders, but has not been investigated in a clinical trial focusing on smoking cessation. Thus, the primary purpose of the proposed study will be to investigate the effects of a low-cost prize-based form of contingency management in the treatment of nicotine dependence. To accomplish this objective, we enrolled 103 current smokers into the study. The participants in Study Arm 1 received the contingency management intervention for 8 weeks, and the participants in Study Arm 2 had their smoking status assessed but did not receive the contingency management intervention. Both interventions received brief counseling and nicotine replacement therapy. The counseling was conducted in two 60-minute individual sessions scheduled one week apart with two follow-up phone calls at weeks 3, 4, and 6.
The primary outcome for this study was biochemically-validated smoking status at 3 months (end of treatment), and at 6- and 12-month follow-up. Both continuous and point-prevalent abstinence rates were determined. Saliva cotinine levels were measured in all participants reporting abstinence at each assessment. This study had 80% power to detect a 10% absolute difference in smoking cessation rates between the two treatment conditions (i.e., a 28% quit rate in Study Arm 1 versus a 18% quit rate in Study Arm 2) with alpha set at 0.05. These estimates included an anticipated 15% loss to follow-up over the 12-month study period.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Abstinence Rate |
8; 10 | — |
Eligibility Criteria
Inclusion Criteria
- Smoke at least 5 cigarettes per day
- Interested in quitting
Exclusion Criteria
- Cognitive impairment or unstable psychotic disorder that would significantly interfere with the individual's ability to participate in the study.
- Self-reported problem with alcohol or other drugs during the past three months
- Current use of any smoking cessation medication
- Presence of any contraindications for nicotine patches, lozenges, or gum
- Pregnancy
Data sourced from ClinicalTrials.gov (NCT01040260). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.