The purpose of the study is to develop and test an Internet-based group contingency management program designed to promote smoking cessation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
40
This group (n = 20) will earn vouchers based only on team (n = 4) performance. Only if all members of the team submit a negative sample (CO ≤ 4 ppm), will they each earn a voucher.
This group (n = 20) will earn vouchers based on both individual and team (n = 4) performance. If an individual submits a negative sample (CO ≤ 4 ppm), s/he will earn a voucher. Additionally, bonus vouchers will be earned if all team members submit negative samples.
University of Florida
Gainesville, Florida, United States
National Development and Research Institutes
New York, New York, United States
Breath CO
Twice daily breath CO samples obtained during baseline and treatment
Time frame: 8 weeks
Point prevalence measure of abstinence
Abstinence will be defined as: (a) CO sample ≤ 4 ppm; (b) cotinine \< 50 ng/ml; and (c) reporting not smoking, not even a puff in the last 7 days.
Time frame: at the end of treatment (approximately week 4) and at 3 month follow-up
Duration of abstinence during treatment.
The longest duration of sustained abstinence (CO ≤ 4 ppm) based on the twice-daily breath samples during the treatment period.
Time frame: 3 weeks
Rate of social exchanges
The number of comments posted on the discussion forum during treatment.
Time frame: 3 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.