Evaluation of a Computer-Delivered 5 A's Intervention for Smoking
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About
This is a 2-group RCT in 380 tobacco-using medical patients that will compare a single session, computer-directed 5 A's intervention for smoking (experimental condition) to screening and resource provision (control condition). Follow-up visits will occur at 1 and 3 months post study enrollment. Measures will focus on tobacco use and related psychosocial outcomes (e.g. mood, stress). We will compare resources used and economic costs needed to implement each intervention.
The Investigators hypothesize that patients receiving the computer-directed intervention will have significantly higher tobacco abstinence rates at 3 months post study enrollment compared to the control group. If indeed the computerized intervention increases tobacco abstinence rates compared to the control group, this intervention could be used to increase access to treatment for the millions of US smokers, ultimately reducing tobacco mortality and morbidity rates in this country.
Enrollment
Sex
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Volunteers
Inclusion criteria
- 18 - 65 years
- Primary care patient
- Smoked at least one cigarette per day for the past seven days or at least 10 cigarettes total during the past week
- Smoked at least 100 cigarettes (lifetime)
- Had no recent (past 90 days) use of other forms of tobacco (pipes, cigars, NRT)
- Able to speak English
Exclusion criteria
- Pregnant
Trial design
Primary purpose
Allocation
Interventional model
Masking
8 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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