Smartphone-based Incentives Intervention to Increase Smoking Cessation During Pregnancy

Part of paid clinical trials in Burlington, Vermont.

Sponsor
University of Vermont
Study ID
NCT07840118
Status
Not Yet Recruiting

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Conditions

  • Perinatal Cigarette Smoking
  • Smoking During Pregnancy and Postpartum

Eligibility Criteria

Sex
FEMALE
Age
18 Years - 50 Years
Healthy Volunteers
Not accepted

Interventions

  • Best Practices — BEHAVIORAL
    Participants receive the 5As including a staff referral to the state tobacco quitline.
  • Financial Incentives — BEHAVIORAL
    Participants receive financial incentives contingent on biochemically verified abstinence. Incentives are in the form of vouchers exchangeable for retail items and available through 12-weeks postpartum.

Study Details

Cigarette smoking is the leading preventable cause of poor pregnancy outcomes in the U.S. and a problem for which more effective and easy-to-access treatments are much needed. This study examines whether outcomes achieved with recommended clinical practices (referral to state tobacco Quitline with follow-up and further referrals for those continuing to smoke) can be improved by also offering financial incentives delivered through a smartphone for maternal smoking abstinence.

Key Dates

First listed
Sep 24, 2026
Start date
Sep 30, 2026
Status verified
Sep 2026
Primary completion
May 31, 2028
Completion
May 31, 2028

Study Design

Enrollment
137 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Best Practices
    Best Practices (BP) entails the 5As including referral to the state tobacco Quitline and further referral for those continuing to smoke.
  • Experimental: Best Practices plus Financial Incentives
    Best practices plus providing financial incentives contingent on biochemically verified abstinence. Incentives are in the form of vouchers exchangeable for retail items and available through 12-weeks postpartum.

Primary Outcome Measure

Antepartum smoking abstinence [ Time Frame: Antepartum period is from study entry through infant delivery which is typically about 24 weeks duration. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of VermontBurlingtonVermont05464-

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