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Not yet recruiting NCT07356297

Remote Interventions for Menthol Cigarette Use

No phase Interventional Cigarette Smoking

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Quitline (QL), Mobile incentive-based intervention.
Who it may be relevant to
Registry conditions: Cigarette Smoking. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparing Remotely-delivered Interventions to Promote Cessation Among Adults Who Smoke Menthol Cigarettes

Overview

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.

Interventions

  • Behavioral Quitline (QL)
    QL services include scheduled and on-demand phone and digital interactions with a coach, as well as optional ancillary services and nicotine replacement therapy by mail.
  • Behavioral Mobile incentive-based intervention
    The app-based intervention incentivizes participants for daily check-ins, smoking cessation, and QL calls. Participants also receive encouragement to set a smoking quit date from a study interventionist and receive motivational messages in the app.

Primary outcome measures

  • Smoking Cessation [Time frame: 3-, 6-, 9- and 12- months post baseline]
Secondary outcome measures (1)
  • Smoking Cessation With Lapses [Time frame: 3-, 6-, 9- and 12- months post baseline]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07356297 · HUM00275412 · SU-2024C2-40036

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗