CClinicalTrials.gg
CompletedNCT06689774Updated Sep 9, 2026

Salvation Army Tobacco Quit Line Referral Implementation Trial

An interventional study of Cognitive-Motivational Feedback and Staff Tobacco Quit Line Referral Implementation Support in Tobacco Use, Smoking and Smoking Cessation, sponsored by University of Wisconsin, Madison. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-09.

Sponsored by University of Wisconsin, Madison · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
96
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
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Study summary

The goal of this clinical trial is to understand how the Salvation Army staff can help people who use tobacco learn about and connect with no-cost treatments to help cut down or quit smoking. Researchers will gather information about the thoughts and experiences of people who smoke tobacco and receive services at the Salvation Army, as well as the experiences of the staff offering support to help treat tobacco use.

Read the detailed description

In this 2-year pilot study, a team of Salvation Army personnel and consumers will work with a member of the University of Wisconsin Center for Tobacco Research and Intervention Regional Outreach team to plan, implement, and evaluate strategies to connect Salvation Army service consumers with the Wisconsin Tobacco Quit Line for help quitting smoking. The study team will pilot test and refine an enhanced implementation support protocol designed to help Salvation Army teams adapt quitline referral workflows and implementation strategies to fit well with the culture and climate of participating Salvation Army sites, and to enhance Salvation Army staff readiness to connect the consumers they serve with the Wisconsin Tobacco Quit Line. The study team will also pilot test and refine a strategy that Salvation Army personnel can use to incentivize acceptance of Wisconsin Tobacco Quit Line connections by consumers while they are at the Salvation Army service center. To evaluate and enhance the 2 implementation strategies of interest in this study (enhanced implementation support for personnel and an incentive for consumers to accept a connection with the Quit Line while at the Salvation Army), the study team will conduct qualitative interviews with both personnel and consumers at Salvation Army sites, and will collect survey data from personnel and consumers. Service records from both the Salvation Army and Wisconsin Tobacco Quit Line will also be collected for this study to help evaluate the reach of the tobacco treatment intervention, and the representativeness of its reach across subpopulations of consumers. Data regarding the process of implementing Wisconsin Tobacco Quit Line referral in the Salvation Army will also be gathered via observation and recordings of project team meetings. These sources of data will be integrated to help evaluate how well the strategies of interest work in 2 Salvation Army sites, and to refine these in preparation for a full-scale cluster-randomized clinical trial.

02

Conditions studied

  • Tobacco Use
  • Smoking
  • Smoking Cessation

Keywords

  • Salvation Army
03

In context

Tobacco Use

125 studies on the registry are indexed under Tobacco Use; 64 are open to participants now.

This study's enrollment of 96 is below the median of 150 across 119 interventional studies indexed under Tobacco Use.

Browse Tobacco Use studies →

Lead sponsor

University of Wisconsin, Madison is the lead sponsor of 1,161 studies on the registry; 182 are open to participants now.

Of its 151 completed or terminated interventional studies of FDA-regulated products, 114 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age 18 or older
  • Involved in the management, delivery, or receipt of social services offered by a participating Salvation Army site, or a member of the University of Wisconsin-Center for Tobacco Research and Intervention Outreach Team supporting Wisconsin Tobacco Quit Line implementation
  • Able to speak English, Spanish, or another language for which an interpreter is available

Exclusion criteria

Exclusion Criteria:

  • Children under the age of 18
  • Unable to speak a common language with a study team member or available interpreter
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
96 participants (actual)

Study arms

  • Experimental
    Enhanced Wisconsin Tobacco Quit Line (WTQL) Referral Implementation Support

    Both participating sites in this pilot study will be in this experimental enhanced implementation support arm to help us iteratively enhance the feasibility, acceptability, and sustainability of implementation strategies to support WTQL referral in these sites. Salvation Army personnel at participating sites will receive implementation training and ongoing support to help enhance the fit of WTQL referral in their workflows, culture, and climate, and to enhance staff readiness to connect the consumers they serve with the WTQL. No consumer incentives for connecting with the Quit Line immediately by phone will be offered in this arm so it can serve as active comparator condition for the incentivized arm described below.

    Behavioral: Cognitive-Motivational Feedback · Behavioral: Staff Tobacco Quit Line Referral Implementation Support

  • Experimental
    Incentivized Immediate Wisconsin Tobacco Quit Line (WTQL) Referral

    In this experimental condition, Salvation Army personnel will implement an incentive strategy designed to encourage Salvation Army consumers to accept immediate referral to the WTQL. The incentive strategy will be adapted by Salvation Army personnel to fit in the local context, and staff will receive training and ongoing support in implementation of the incentive strategy. The modest incentives will be added in a staggered manner across the 2 Salvation Army sites participating in this pilot trial, after at least 3 months of implementing WTQL referral without consumer incentives for immediate calls.

    Behavioral: Cognitive-Motivational Feedback · Behavioral: Staff Tobacco Quit Line Referral Implementation Support · Behavioral: Consumer Incentives for Immediate Referral to a Tobacco Quit Line

Interventions

  • BehavioralCognitive-Motivational Feedback

    Salvation Army personnel will be trained to offer adult consumers who use tobacco cognitive-motivational feedback about tobacco use via a no-cost, web-based Qualtrics survey that assesses participant knowledge, beliefs, and priorities and provides feedback to promote knowledge of the costs and risks of smoking and knowledge of the costs and benefits of tobacco use treatment options, including Wisconsin Tobacco Quit Line services. The survey is also designed to help participants weigh the importance of the pros and cons of continuing to use tobacco, and the pros and cons of trying to change their tobacco use.

  • BehavioralStaff Tobacco Quit Line Referral Implementation Support

    Salvation Army personnel will receive training and will be engaged in efforts to plan, evaluate, adapt, and sustain tobacco treatment referral as part of the social services they provide to adult Salvation Army service consumers who use tobacco. Implementation support will take the form of ongoing engagement of an outreach specialist with a team of Salvation Army personnel and consumers who lead Quit Line referral efforts in the Salvation Army.

  • BehavioralConsumer Incentives for Immediate Referral to a Tobacco Quit Line

    Salvation Army personnel will offer an incentive to adult consumers who use tobacco to encourage immediate acceptance of a live call with the Wisconsin Tobacco Quit Line. The incentive will be designed by Salvation Army personnel to fit the local context and to be sustainable over time, such as extra access to existing support or resources.

06

What researchers measure

Primary outcomes

  1. Wisconsin Tobacco Quit Line (WTQL) referral rate

    Proportion of adult Salvation Army consumers who use tobacco referred to the WTQL in any modality. Goal is at least 10% without incentives, and at least 16% with incentives.

    Time frame: 18 months

  2. Wisconsin Tobacco Quit Line (WTQL) enrollment rate

    Proportion of clients referred from Salvation Army sites that enroll in WTQL services. Goal is at least 5% without incentives, 8% with incentives.

    Time frame: 18 months

  3. Salvation Army personnel WTQL referral training engagement

    Proportion of eligible Salvation Army personnel who participate in at least some WTQL referral training. Goal is at least 70%.

    Time frame: 18 months

  4. Tobacco use screening of adult consumers of Salvation Army services

    Rate of asking about and documenting current tobacco use among all adult consumers of eligible services in participating Salvation Army sites. Goal is 50% screening rate.

    Time frame: 18 months

Secondary outcomes

  1. Self-reported abstinence from smoking in the past 7 days

    Number of WTQL service clients referred from the Salvation Army who report no smoking in the past 7 days at follow-up

    Time frame: 3 months, 6 months post target date to quit smoking

  2. Immediate referral via live calls to Wisconsin Tobacco Quit Line (WTQL)

    Rate of immediate referral via live calls to WTQL among adult Salvation Army consumers who use tobacco (this will be a subset of the primary referral outcome)

    Time frame: 18 months

  3. Salvation Army personnel adoption of WTQL referral

    Proportion of eligible Salvation Army personnel who refer at least 1 client to the WTQL. Goal is at least 60%.

    Time frame: 18 months

  4. Cost per successful WTQL referral

    Estimated cost of successfully connecting a Salvation Army consumer with the WTQL, with and without incentives for immediate WTQL connection

    Time frame: 18 months

07

Study locations

1 site
  • University of Wisconsin Center for Tobacco Research and Intervention
    Madison, Wisconsin 53711, United States
08

References and documents

Study documents

  • Informed consent form · Oct 29, 2024

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — Deidentified individual-level original data collected in this trial will be shared. Aggregate data on Salvation Army and Wisconsin Tobacco Quit Line data used in analyses for this trial will also be shared.

Supporting information: Study protocol, Sap, Icf, Analytic code

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06689774
Lead sponsor
University of Wisconsin, Madison
Collaborators
National Institutes of Health (NIH), National Cancer Institute (NCI)
Responsible party
Sponsor
First posted
Nov 14, 2024
Start date
Nov 1, 2024
Primary completion
Jun 30, 2026
Completion
Aug 31, 2026
Last update
Sep 9, 2026

Study contacts

Danielle McCarthy, PhD
principal investigator · University of Wisconsin, Madison

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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