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Striving to Quit-Wisconsin Tobacco Quit Line

Striving to Quit: Wisconsin Tobacco Quit Line Tobacco Cessation Research

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01569477
Enrollment
0
Registered
2012-04-03
Start date
2012-09-30
Completion date
2013-03-31
Last updated
2016-12-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nicotine Dependence, Smoking, Smoking Cessation

Brief summary

This study is designed to test the hypotheses that incentives can increase both participation in smoking cessation treatment and resulting cessation rates when they are offered to Medicaid BadgerCare Plus members.

Detailed description

Aim 1: To determine the extent to which contingent financial treatment incentives (i.e., incentives for biochemical verification visits, treatment engagement, and abstinence) versus attendance incentives (i.e., incentives for only attending the biochemical verification visits), increase rates of smoking cessation . Participants will be BadgerCare Plus tobacco users who enroll in Wisconsin Tobacco Quit Line (WTQL) services. Aim 2: To determine the extent to which treatment incentives vs. attendance incentives increase rates of engagement in smoking cessation treatment through the WTQL when offered to BadgerCare Plus members who smoke. Aim 3: To determine the cost-effectiveness of the smoking cessation program when paired with treatment incentives and when paired with attendance incentives. Aim 4: To identify moderating and mediational effects regarding the clinical benefit of incentivized smoking treatment Aim 5: To determine the reach of an incentivized smoking cessation treatment that depends upon primary care clinic staff, a fax-to-quit referral mechanism and a state quit line.

Interventions

Treatment incentives - incentives for biochemical verification visits, treatment engagement and abstinence

Attendance Incentives - incentives for only attending the biochemical verification visits

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* enrollment in Wisconsin Medicaid (BadgerCare Plus) * resides in study area (one of 25 counties) * member of participating HMOs * 18 or older * English 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) every 6 months (3 times over a 12 month period), provide urine samples, and complete follow-up phone calls * 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 * not a member participating HMOs * less than 18 years of age * not English 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) every 6 months (3 times over a 12 month period), provide urine 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.

Design outcomes

Primary

MeasureTime frameDescription
Abstinence from smokingMeasured 6 months after enrollment at follow-up assessmentThe data will be the biochemically confirmed reports of abstinence for the past 7 days (i.e., 7-day point-prevalence abstinence)

Secondary

MeasureTime frameDescription
Engagement in treatmentMeasured 12 months after enrollment at follow-up assessmentThe primary analyses will compare number of calls completed
Cost-effectivenessMeasured 12 months after enrollmentThe primary analysis will contrast the incremental costs of the treatment vs. attendance conditions by computing the Incremental Cost-Effectiveness Ratio (ICER) with regard to attaining 6-month abstinence.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026