Suspended

Incentives for Participation Versus Outcomes for Population Cessation of Smoking

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What is being tested

Incentives for Participation

+ Incentives for Cessation

Behavioral
Who is being recruted

Behavior

+ Smoking

Over 18 Years
See all eligibility criteria
How is the trial designed

Services Research Study

Interventional
Study Start: March 2014
See protocol details

Summary

Principal SponsorUniversity of Rhode Island
Last updated: April 17, 2025
Sourced from a government-validated database.Claim as a partner

Study start date: March 1, 2014

Actual date on which the first participant was enrolled.

This population-based randomized clinical trial is designed to compare long-term abstinence rates in three groups of smokers: 1. Those incentivized for participation in an evidence-based treatment designed for smokers at each stage of change; 2. Those incentivized for biologically validated prolonged abstinence at 6 and 12 months who could also choose to participate in the TTM (Transtheoretical Model)-tailored intervention; and 3. An assessment only control condition. The Specific Aims are: To assess whether the treatment group incentivized for participation outperforms the control group at 12, 24 and 36 months as hypothesized; To assess whether the treatment group incentivized for prolonged abstinence at 6 and 12 months outperforms the control group at each follow-up as hypothesized; To assess whether the treatment group incentivized for participation outperforms the treatment group incentivized for outcomes at 36 months as hypothesized. To compare the cost-effectiveness of each treatment in a population of mostly unmotivated smokers; The Secondary Aims are: To assess the long-term treatment trajectories of each treatment compared to controls with hypothesized increasing trajectory in the participation contingent incentives and decreasing trajectory in the outcome contingent incentives. To identify mediators of long-term outcomes in each treatment, such as amount of treatment participation, income, severity of smoking, stage of change, self-efficacy, perceived health and intrinsic and extrinsic motivation to quit. To compare cost-savings of each treatment by modeling all additional costs of smoking for employers and smokers.

Principal SponsorUniversity of Rhode Island
Last updated: April 17, 2025
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Services Research Study

These studies look at how healthcare is delivered, managed, and organized. They aim to improve care quality, patient experience, and access to treatment.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorSmoking

Criteria

Inclusion Criteria: smoker Exclusion Criteria: -

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

No Intervention
Participants will be incentivized for assessments only

Group II

Experimental
Participants will be incentivized for each assessment and for each smoking cessation session they complete

Group III

Experimental
Participants will be incentivized for each assessment and biochemically confirmed abstinence at 12 and 24 months

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

University of Rhode Island

Kingston, United StatesOpen University of Rhode Island in Google Maps
SuspendedOne Study Center