Factorial Design to Assess Quit-line Connections

November 28, 2018 updated by: Michael Parks, Minnesota Department of Health

Financial Incentives and Proactive Calling for Reducing Barriers to Tobacco Treatment Among Socioeconomically Disadvantaged Populations: A Factorial Randomized Trial

Improved strategies and scalable interventions to engage low-socioeconomic status (SES) smokers in tobacco treatment are needed. The investigators tested an intervention designed to connect low-SES smokers to treatment services, implemented through Minnesota's National Breast and Cervical Cancer Early Detection Program (Sage) in 2017. Participants were female smokers from Sage (N=3,365). Using a factorial design, participants were randomized to six intervention groups consisting of a proactive call (no call vs call) and/or a financial incentive offered for being connected to treatment services (three levels of incentives). All individuals received direct mail and could opt for cessation support through Minnesota's population-based cessation services. The primary outcome was confirmed connection via phone to the free quit-line.

Study Overview

Detailed Description

Individuals were randomized to one of six conditions. The design was a two-factor, three-by-two factorial design: three levels of financial incentives, and two levels of proactive calls (yes, no). All groups received direct mail and free tobacco treatment services.

The intervention was implemented from June 2017 to October 2017. National Breast and Cervical Cancer Early Detection Programs serve uninsured women with household incomes at or below 250% of the U.S. federal poverty level; subsequently, the sample was strictly female, and the investigators included individuals for whom self-reported smoking status was available (from 2014 to 2017). Smoking status was determined using Sage data, which come from clinics and Sage's call center. Using a uniform measure ("Does the participant currently smoke cigarettes?"), smoking status was based on cigarette use at the time of contact with the Sage program (i.e., clinic visit or contact with the call center). Data on smoking intensity were not available. There were 3,723 smokers who met selection criteria.

All participants received two rounds of direct mail. Mailers consisted of a folded card, which contained messages and graphics rooted in a loss-frame approach. Following previous research, the loss-frame approach was designed to indicate that certain behaviors lead to unhealthy outcomes, and the investigators paired the message with a clear articulation of behavioral steps.

Sage has a call center staffed by patient navigators. When participants called Sage's number, patient navigators followed a script, recorded callers' promotion code, determined callers' desire to participate, and made connections to the quit-line for willing participants. After two rounds of direct mail, patient navigators placed proactive outreach calls to eligible participants. Phone numbers were retrieved from the Sage database. Using a script, navigators reminded participants of the direct mail piece and the program offer. Each participant received one proactive call. One call attempt was made; navigators left a voicemail for participants who were unavailable. Proactive calling lasted three months.

Both the mailer and navigators referred participants to Minnesota's free population-based cessation services. The quit-line is funded and administered by an independent nonprofit organization. Participants can enroll in services either by phone or online. Tobacco users can choose telephone counseling or one or more individual services.

Our primary outcome was phone-only treatment connection, which was defined as a confirmed connection between participants and quit-line staff via three-way calls conducted by patient navigators. For willing participants, patient navigators called quit-line staff and confirmed that a patient would be connected via a three-way call. Navigators remained on the line until communication between participants and quit-line staff was established. Once connected, trained operators from the quit-line were responsible for administering cessation-related services.

A secondary measure captured connections to online services. This measure combined both phone and web connections. The web connection assessed whether participants entered their individual promotion codes (provided via direct mail) on a unique online landing page. Once participants entered their individual codes, they were directly connected to the cessation webpage where they entered their personal information and chose tailored treatment services. Direct transfers to the online services counted as a connection; each code was counted only once. The investigators used the confirmed phone connection as our primary outcome as it was a more conservative measure of connection to tobacco treatment services. The investigators used the measure that combined phone and web connections in secondary analyses.

Intervention components. The investigators used dummy variables to assess levels of financial incentives (for all three measures: 1=yes, 0=no). The proactive calling measure was assessed using a dichotomous measure (1=proactive calling, 0=no proactive calling). The investigators assessed the components' combined effect by generating interaction terms.

Covariates. The investigators examined whether randomized groups differed according to age (continuous measure ranging from 20 to 88), race/ethnicity (five dichotomous measures: white, African American, Hispanic, American Indian, and other races/ethnicities), whether participants spoke Spanish or not (1=yes, 0=no), whether respondents lived with a fellow smoker (1=yes, 0=no), time since last contact with Sage (four dichotomous variables: 2014, 2015, 2016, or 2017), and urban residence (1=metro region, 0=other).

Using a per-protocol approach, the investigators eliminated all individuals with bad addresses. Descriptive statistics were used to compare connection rates and demographics across intervention arms. The investigators ran a logistic regression model that included dichotomous measures for all six possible treatment conditions in order to run post-estimation pairwise comparisons.

Logistic regression is the optimal method for examining unbalanced factorial designs with a binary outcome. The investigators ran four logistic regression models for the primary analysis. The investigators examined: (1) the association between incentive levels and phone-only quit-line connections, (2) the association between proactive calling and phone-only quit-line connections, (3) the direct effects of financial incentives and proactive calling, and the interaction between incentive levels and proactive calling, and (4) the effect of intervention components adjusted for covariates. For the logistic regression models, the main effects for the incentive and proactive call are interpreted as the effect when all other variables equal zero, and the interaction coefficients are interpreted as the test for whether the relationship between proactive calling and connections to the quit-line depended on receiving an incentive. For the secondary analyses, the investigators report in the text any differences between the phone-only measure and the combined measure that combined telephone and web connections.

For cost-effectiveness analysis, the investigators assessed the average cost-effectiveness ratio, which is the increase in costs by each intervention group compared with the no incentive, no call group, divided by the increase in connections within each intervention group compared with the no incentive, no call group. The investigators also examined the incremental cost-effectiveness ratios, which is the change in cost compared to an adjacent condition divided by the change in connections compared to the adjacent condition. The investigators included costs associated with printing, postage, incentives, labor, and the creation and maintenance of the landing page. Costs were in 2017 US dollars and based on receipts and labor hours; hourly rates were based on national averages for respective positions.

Study Type

Interventional

Enrollment (Actual)

3723

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Minnesota
      • Saint Paul, Minnesota, United States, 55164
        • Minnesota Department of Health

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Uninsured women
  • Household incomes at or below 250% of the U.S. federal poverty levels
  • Individuals who reported smoking (from 2014 to 2017)

Exclusion Criteria:

  • Non-smokers
  • Men
  • Not a National Breast and Cervical Cancer Early Detection Program patient

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Incentive Level High, Call
Using a factorial experimental design, the investigators evaluate how coupling a population-based, direct mail intervention with (1) financial incentives and (2) proactive telephone outreach influences connections to evidence-based tobacco treatment services among low-SES smokers.
Experimental: Incentive Level High, No Call
Using a factorial experimental design, the investigators evaluate how coupling a population-based, direct mail intervention with (1) financial incentives and (2) proactive telephone outreach influences connections to evidence-based tobacco treatment services among low-SES smokers.
Experimental: Incentive Level Medium, Call
Using a factorial experimental design, the investigators evaluate how coupling a population-based, direct mail intervention with (1) financial incentives and (2) proactive telephone outreach influences connections to evidence-based tobacco treatment services among low-SES smokers.
Experimental: Incentive Level Medium, No Call
Using a factorial experimental design, the investigators evaluate how coupling a population-based, direct mail intervention with (1) financial incentives and (2) proactive telephone outreach influences connections to evidence-based tobacco treatment services among low-SES smokers.
Experimental: No Incentive, Call
Using a factorial experimental design, the investigators evaluate how coupling a population-based, direct mail intervention with (1) financial incentives and (2) proactive telephone outreach influences connections to evidence-based tobacco treatment services among low-SES smokers.
Experimental: No Incentive, No Call
Using a factorial experimental design, the investigators evaluate how coupling a population-based, direct mail intervention with (1) financial incentives and (2) proactive telephone outreach influences connections to evidence-based tobacco treatment services among low-SES smokers.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Phone-only treatment connection
Time Frame: 3 months
Our primary outcome was phone-only treatment connection, which was defined as a confirmed connection between participants and quit-line staff via three-way calls conducted by patient navigators (1=yes, 0=no).
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2017

Primary Completion (Actual)

October 31, 2017

Study Completion (Actual)

December 20, 2017

Study Registration Dates

First Submitted

November 26, 2018

First Submitted That Met QC Criteria

November 28, 2018

First Posted (Actual)

November 30, 2018

Study Record Updates

Last Update Posted (Actual)

November 30, 2018

Last Update Submitted That Met QC Criteria

November 28, 2018

Last Verified

November 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • quitplan2018

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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