CClinicalTrials.gg
CompletedNCT05072301Updated Sep 1, 2023

Preliminary Test of Reactive Carrot Incentives in a Practice Quit Environment With Contingency Management Incentives

An interventional study of Contingency Management and Control in Smoking Cessation, sponsored by Yale University. Completed at 2 sites in 2 countries. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-09-01.

Sponsored by Yale University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
87
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The primary aim of this study is to pilot test a novel reactive carrot approach for improving individuals' ability to stick to a "practice quit" program in a smoking cessation context. In this study, the treatment gives subjects an offer to forego a monetary incentive to forego the opportunity to receive subsequent abstention (contingency management) rewards.

Read the detailed description

All the subjects, treatment and control groups, would be given the opportunity to receive attendance rewards for attending six CO testing meetings as well as abstention (contingency management) rewards for abstaining from smoking. The only difference between the subjects randomly assigned to treatment and control groups is that each member of the treatment group would be tempted at the beginning of their program by being offered a one-time monetary incentive to forego the opportunity to receive subsequent abstention (contingency management) rewards. Treatment group subjects would, at their initial intake meeting after the attendance and abstention rewards opportunity had been described, be given a one-time opportunity to received $80 temptation payment to give up the opportunity to receive subsequent abstinence (contingency management) rewards that could be worth as much as $165. Subjects who accepted this one-time opportunity would remain enrolled in the practice quit smoking and they would still be eligible to receive attendance reward compensation totaling up to $30 for showing up to their six testing appointments. The purpose of the study is to test whether resisting the temptation to accept the one-time payment helps steel the resolve of the treatment subjects to follow through and make sure that they earn the subsequent contingency management rewards. More specifically, an intent-to-treat design will allow us to test whether the temptation causes treatment group subjects to have greater success than the un-tempted control group subjects to abstain from smoking during the two-week practice quit period.

02

Conditions studied

  • Smoking Cessation

Keywords

  • incentives
03

In context

Lead sponsor

Yale University is the lead sponsor of 1,724 studies on the registry; 298 are open to participants now.

Of its 210 completed or terminated interventional studies of FDA-regulated products, 126 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age ≥ 18 years
  • Smoke ≥ 3 cigarettes per week and expressing interest in quitting smoking.

Exclusion criteria

Exclusion Criteria:

  • Unstable psychiatric conditions such as suicidal ideation, acute psychosis, severe alcohol dependence, or dementia
  • unstable medical conditions that have not been well controlled (e.g., acute infection requiring hospitalization) for the past 30 days
  • pregnant or breastfeeding women
  • those with limited decision making capacity.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
87 participants (actual)

Study arms

  • Experimental
    Contingency Management

    The treatment group will receive a onetime offer of $80 (a reactive carrot) to forego all abstinence (contingency management) reward payments in the future.

    Behavioral: Contingency Management

  • Placebo comparator
    Control

    The control group will receive contingency management payments and other monetary benefits for completing the trial.

    Behavioral: Control

Interventions

  • BehavioralContingency Management

    The treatment group will receive a onetime offer of $80 (a reactive carrot) to forego all abstinence (contingency management) reward payments in the future.

  • BehavioralControl

    The control group will receive contingency management payments and other monetary benefits for completing the trial.

06

What researchers measure

Primary outcomes

  1. Breath Carbon Monoxide Test (measured in ppm levels)

    A primary outcome is the sum of times a subject tested abstinent at the 6 CO testing meetings. To test for abstinence, a breath carbon monoxide test will be used to determine exposure to smoke. Abstinence will be coded as expired-air carbon monoxide (CO) levels below 5 ppm.

    Time frame: 14 days following intake date

  2. Proportion of CO (CO ≤ 4ppm)

    Proportion of 6 CO tests showing abstinence (CO ≤ 4ppm)

    Time frame: 14 days following intake date

  3. Maximum number of consecutive abstinent days

    The maximum number of consecutive abstinent days for each subject will be measured

    Time frame: 14 days following intake date

Secondary outcomes

  1. Attrition

    Attrition will be measured by participants ability to make their testing appointments.

    Time frame: 14 days following intake date

  2. Contingency Management Payment

    Total amount of abstention (contingency management) rewards paid to subjects.

    Time frame: 14 days following intake date

  3. Time to first relapse

    Time to first relapse will be measured by subjects self-reporting use of different types of tobacco products or cigarette alternatives

    Time frame: 14 days following intake date

  4. Reduced smoking

    Whether subjects report reduced smoking will be used to measure reduced smoking habits

    Time frame: 14 days following intake date, as well as 1 month and 6 months after intake date

07

Study locations

2 sites
  • General New Haven Public
    New Haven, Connecticut 06512, United States
  • Ukraine site
    Kiev, Ukraine
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 1, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05072301
Lead sponsor
Yale University
Responsible party
Sponsor
First posted
Oct 8, 2021
Start date
Oct 13, 2021
Primary completion
Jan 3, 2023
Completion
Jan 3, 2023
Last update
Sep 1, 2023

Study contacts

Ian Ayres, PhD
principal investigator · Yale Law School
Giuseppe Mattiacci, PhD
principal investigator · University of Amsterdam

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2023. You cannot join it, but the record below documents what was studied.

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