Smoking Cessation Clinical Trial
Official title:
Wisconsin Tobacco Quit Line Centers for Medicaid Services Striving To Quit Evaluation Project
Verified date | April 2017 |
Source | University of Wisconsin, Madison |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study is designed to test the hypotheses that financial incentives can increase both participation in smoking cessation treatment and resulting cessation rates, when they are offered to BadgerCare Plus (Medicaid) smokers as part of their health care.
Status | Completed |
Enrollment | 1900 |
Est. completion date | March 2017 |
Est. primary completion date | March 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 99 Years |
Eligibility |
Inclusion Criteria: - enrollment in Wisconsin Medicaid (BadgerCare Plus) - resides in study area (one of 25 counties) - 18 or older - English or Spanish speaking - has smoked daily (at least 5 cigarettes each day) over the last week - willingness to attend visits at his/her PCC (primary care clinic) or go to a testing site at baseline and 6 months (2 times over a 6 month period), provide urine samples or participate in exhaled carbon monoxide testing, and complete follow-up phone calls from the WTQL - willingness to inform the WTQL as to any change in address, phone number, clinic attended, or health plan. Exclusion Criteria: - not enrolled in Wisconsin Medicaid (BadgerCare Plus) - not reside in study area - less than 18 years of age - not English or Spanish speaking - does not smoke daily (at least 5 cigarettes each day) over the last week - not willing to attend visits at his/her PCC (primary care clinic) or alternative testing site at baseline and 6 months (2 times over a 6 month period), provide urine or exhaled carbon monoxide samples, and complete follow-up phone calls. - not willing to inform the WTQL as to any change in address, phone number, clinic attended, or health plan. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Wisconsin, Madison |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Abstinence From Smoking | The primary outcome data will be the biochemically confirmed abstinence using urine (measured cotinine) or exhaled (breath) carbon monoxide (CO). | Measured 6 months after enrollment at follow-up assessment | |
Secondary | Engagement in Treatment | This analysis will compare number of calls completed | Measured 6 months after enrollment at follow-up assessment | |
Secondary | Cost-effectiveness | This analysis will quantify the costs of treatment for Control and Incentive conditions with regard to attaining 6-month abstinence. Project costs were allocated to three categories: 1) Service costs, including billed staff time for counseling and testing, as well as all incidentals connected with services; 2) Incentives and distribution costs; and 3) Service-related administrative costs, including promotion/marketing and staff time for administering the intervention. Costs of planning the project, grant administration, and research within the project are not included in the analysis.The outcome is the cost per quit in each treatment group. Cost per quit in each group was calculated by: 1) computing the grand total of costs for all participants in a given group; and 2) dividing the grand total for a given group by the number of successful quitters. As such, the cost per quit is a single value with no measure of dispersion. | Measured 6 months after enrollment |
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