RECRUITING

Contingency Management to Promote Smoking Cessation

Description

Many hospitals and outpatient clinics often refer people who smoke to quitlines and provide prescriptions for smoking cessation medications, but patients rarely fully engage in counseling or use their cessation medications. This is a single-arm, open-label pilot study to provide feasibility metrics for a text-based contingency management (CM) intervention to increase engagement in smoking cessation treatment. All participants (N=20) will be referred to a state quitline and will receive a prescription for medication plus 12 weeks of a text-based CM intervention to increase engagement in quitline calls and varenicline utilization. The engagement of participants in quitline counseling will be tracked for 6 weeks and medication utilization for 12 weeks post-enrollment. The investigators will use mixed-methods to collect implementation and acceptability data to inform changes to the text-based contingency management (CM) intervention.

Study Overview

Study Details

Study overview

Many hospitals and outpatient clinics often refer people who smoke to quitlines and provide prescriptions for smoking cessation medications, but patients rarely fully engage in counseling or use their cessation medications. This is a single-arm, open-label pilot study to provide feasibility metrics for a text-based contingency management (CM) intervention to increase engagement in smoking cessation treatment. All participants (N=20) will be referred to a state quitline and will receive a prescription for medication plus 12 weeks of a text-based CM intervention to increase engagement in quitline calls and varenicline utilization. The engagement of participants in quitline counseling will be tracked for 6 weeks and medication utilization for 12 weeks post-enrollment. The investigators will use mixed-methods to collect implementation and acceptability data to inform changes to the text-based contingency management (CM) intervention.

Using Contingency Management to Promote Adherence to Smoking Cessation Treatment

Contingency Management to Promote Smoking Cessation

Condition
Smoking Cessation
Intervention / Treatment

-

Contacts and Locations

Kansas City

University of Kansas Medical Center, Kansas City, Kansas, United States, 66103

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Smoked in the past 30 days
  • * Smoke at least 1 cigarette per day when they smoke
  • * ≥ 18 years old
  • * Kansas resident
  • * Speak/read English
  • * Access to a mobile phone
  • * Mobile phone receives text messages
  • * No varenicline contraindications (no acute renal impairment)
  • * Insurance coverage for varenicline
  • * Have no significant co-morbidity (i.e., life-threatening illness, communication barriers or altered mental status)
  • * Cognitively able to participate
  • * Physically able to participate
  • * Not pregnant/breastfeeding
  • * Medically ineligible for varenicline
  • * Patient on smoking cessation medication within 2 weeks of admission date
  • * Patient already talked to quitline in the past 2 weeks.
  • * Patients participating in other quit smoking program or research study

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Kansas Medical Center,

Study Record Dates

2025-09