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RecruitingAccepts healthy volunteersPhase 2

Trial of Varenicline With Nicotine Lozenges and a Smartphone Medication Adherence Intervention for Smoking Cessation

University of Oklahoma · with National Cancer Institute (NCI), Brown University · NCT07099638

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
$92 per visit“Participants will be compensated $1 per day for the completion of daily diary assessments over the first 13 weeks of the study (up to up $92).”
Who can join
Ages 18+ · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Phase 2
Target enrollment
496
US sites recruiting
1
Study start
July 21, 2026
Record last updated
August 19, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

No published studies to date have evaluated the combined impact of varenicline and oral nicotine replacement therapy (NRT) on smoking cessation in a randomized trial. Oral NRT, such as nicotine lozenges, can provide acute relief from cravings/withdrawal, and offers individuals the flexibility to deliver nicotine quickly, in contrast with the continuous, passive, and slow-acting delivery of the nicotine patch. Nevertheless, in clinical trials of other combination pharmacotherapies, participants' adherence to of oral NRT has been suboptimal, making it difficult to determine whether there is an added benefit. Given the near-ubiquity of smartphone ownership (85% of U.S. adults), it is plausible that smartphone-based medication adherence interventions could have a positive influence on pharmacotherapy adherence and smoking cessation. This investigative team has demonstrated the feasibility and potential efficacy of using combination varenicline plus oral NRT treatment to promote smoking cessation in a pilot factorial randomized trial. Likewise, pilot findings showed that medication adherence and smoking cessation rates were higher among those who received smartphone-based medication reminders than those who did not. The proposed study will enroll 496 adults who smoke cigarettes daily. The study will employ a 2x2 factorial design in which participants will be randomized to one of four combinations of two treatment factors: 1) pharmacological treatment (varenicline + nicotine lozenges vs. varenicline alone) and 2) smartphone medication adherence intervention (smartphone-based smoking cessation app with vs. without adherence components). The primary study outcomes will be biochemically-confirmed 7-day point prevalence abstinence at 26 weeks after a scheduled quit date, and medication adherence over the 13-week treatment period. Smartphone-based daily diaries will be employed to assess daily smoking and medication adherence. Notably, the proposed study will employ entirely remote assessment and treatment delivery strategies. Exploratory analyses will evaluate the potential interaction between medication type and the smartphone adherence intervention, and compare the influences of pharmacological treatment type and the medication adherence intervention on weekly physical symptoms (e.g., withdrawal, medication side effects). The overarching goal of the proposed research is to improve smoking cessation treatment and decrease cancer risk.

Being studied: Varenicline (VAR); Nicotine lozenge (NRT); Smartphone intervention with adherence components (COMBO-A); Smartphone intervention without adherence components (COMBO-B); Telephone Counseling

Conditions: Smoking Cessation

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Able to provide documentation of identity (to prevent fraudulent enrollment) and Oklahoma residence (due to limitations on prescribing to out-of-state residents)
  • Reports daily smoking ≥5 cigarettes per day
  • Provides a breath CO sample ≥6ppm to verify current smoking
  • Willing to schedule a smoking cessation attempt within the next 1-2 weeks
  • Willing to abstain from smoking cannabis or other combustible products during the study
  • Willing to use varenicline and nicotine lozenges
  • Willing to participate in the study for ≈6 months
  • Able to demonstrate >6th grade literacy which is necessary to read intervention materials and complete study assessments

Exclusion Criteria

  • Does not own a smartphone that is compatible with the study app
  • Using an FDA-approved smoking cessation medication within the past 30 days
  • Using oral nicotine products (e.g., pouches, chewing tobacco, snus) more than once per week (5+ times) during the past 30 days
  • History of seizures (varenicline contraindication)
  • History of allergic reaction to varenicline
  • Pregnant, planning to become pregnant, or currently breastfeeding
  • Unwilling or unable to use varenicline or nicotine lozenges for other reasons (e.g., severe dry mouth, past history of severe medication side effects)
  • Other medical reasons at the discretion of the prescribing physician (e.g., uncontrolled hypertension, recent myocardial infarction)
  • Weekly or more frequent use of combustible cannabis during the past 30 days with a score ≥2 on the Cannabis Use Disorder Identification Test-Short Form

Recruiting US locations

  • TSET Health Promotion Research Center

    Oklahoma City, OK 73104

    Site contact: Shannon Gwin, Ph.D. · 405-271-8001 · Shannon-Gwin@ou.edu

Study contacts (from the official record)

  • Shannon Gwin, Ph.D. · (405) 271-8001 · Shannon-Gwin@ou.edu
  • Sharon Glassman · (405) 271-8001 · Sharon-Glassman@ou.edu
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