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Remote Interventions for Menthol Cigarette Use

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University of Michigan

Status

Begins enrollment in 2 months

Conditions

Cigarette Smoking

Treatments

Behavioral: Quitline (QL)
Behavioral: Mobile incentive-based intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT07356297
HUM00275412
SU-2024C2-40036 (Other Grant/Funding Number)

Details and patient eligibility

About

The purpose of this study is to evaluate whether a digital, incentive-based program, used in conjunction with traditional quitline (QL) services, can be beneficial to quitline callers who smoke menthol cigarettes. The services evaluated focus on coaching, support, and/or incentives for individuals who wish to quit smoking.

Enrollment

1,200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • adults (ages 18+) who call partnered quitlines (QL); and
  • currently smoke menthol cigarettes; and
  • are fluent in English; and
  • plan to live in the United States for the full trial duration; and
  • have daily smartphone access (including data access) or are willing to use a study-provided smartphone and data plan
  • ability to provide informed consent

Exclusion criteria

  • not ready to set a quit date within 30 days; or
  • have not smoked in the past 7 days
  • Inability to speak/understand English
  • Conditions precluding informed consent or understanding of intervention or assessment content
  • PI discretion

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

1,200 participants in 2 patient groups

Quitline (QL)
Active Comparator group
Description:
Participants complete QL services
Treatment:
Behavioral: Quitline (QL)
Quitline (QL) + App
Active Comparator group
Description:
Participants complete QL services and download our incentive-based mobile app
Treatment:
Behavioral: Mobile incentive-based intervention
Behavioral: Quitline (QL)

Trial contacts and locations

0

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Central trial contact

Simran Dhaliwal, BS; Megan Lavigne, BA

Data sourced from clinicaltrials.gov

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