MedPath

Testing the Decoy Effect to Increase Tobacco Treatment Uptake

Completed
Conditions
Tobacco Smoking
Interventions
Other: Online survey
Registration Number
NCT04200157
Lead Sponsor
NYU Langone Health
Brief Summary

Prior research has shown that the context in which program options are presented to consumer impacts consumer choice (known as the 'decoy effect'). The aims of this study are to: (1) test whether the decoy effect can impact smokers' selection of hypothetical tobacco treatment options; (2) examine sociodemographic moderators of the decoy effect; and and (3) examine whether presenting the time and clinical effectiveness of of the different treatment options modifies the decoy effect.

Detailed Description

The investigators will recruit and conduct a cross-sectional online survey through ResearchMatch (www.researchmatch.org) with 600 tobacco users across the country. The survey will ask participants for their preferences regarding hypothetical tobacco treatment programs. Participants will be randomized to 12 conditions (n=50 per condition). Each condition has a different combination of treatment options. The survey will also assess sociodemographics and tobacco use behaviors. All participants will be asked if they would like to receive information about the state's smoking cessation quitline. Participants who would like to receive information will be given the 1800-QUIT-NOW number and smokefree.gov website address.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
600
Inclusion Criteria
  • Self-reported current tobacco use
Read More
Exclusion Criteria
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
7Online surveyGroup assigned to the following answer combination: 1. 2 sessions (30 minutes) 2. 7 sessions (105 minutes)
5Online surveyGroup assigned to the following answer combination: 1. 2 sessions (30 minutes) 2. 4 sessions (60 minutes)
1Online surveyGroup assigned to the following answer combination: 1. 2 sessions 2. 4 sessions
3Online surveyGroup assigned to the following answer combination: 1. 2 sessions 2. 7 sessions
9Online surveyGroup assigned to the following answer combination: 1. 2 sessions (30 minutes) - 10% chance of quitting 2. 4 sessions (60 minutes) - 30% chance of quitting
11Online surveyGroup assigned to the following answer combination: 1. 2 sessions (30 minutes) - 10% chance of quitting 2. 7 sessions (105 minutes) - 30% chance of quitting
4Online surveyGroup assigned to the following answer combination: 1. 2 sessions 2. 7 sessions 3. 10 sessions
12Online surveyGroup assigned to the following answer combination: 1. 2 sessions (30 minutes) - 10% chance of quitting 2. 7 sessions (105 minutes) - 30% chance of quitting 3. 10 sessions (150 minutes) - 30% chance of quitting
2Online surveyGroup assigned to the following answer combination: 1. 2 sessions 2. 4 sessions 3. 7 sessions
6Online surveyGroup assigned to the following answer combination: 1. 2 sessions (30 minutes) 2. 4 sessions (60 minutes) 3. 7 sessions (105 minutes)
8Online surveyGroup assigned to the following answer combination: 1. 2 sessions (30 minutes) 2. 7 sessions (105 minutes) 3. 10 sessions (150 minutes)
10Online surveyGroup assigned to the following answer combination: 1. 2 sessions (30 minutes) - 10% chance of quitting 2. 4 sessions (60 minutes) - 30% chance of quitting 3. 7 sessions (105 minutes) - 30% chance of quitting
Primary Outcome Measures
NameTimeMethod
Number of weeks until quit date chosen6 months
Number of counseling calls chosen6 months
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

NYU Langone Health - Translational Research Building

🇺🇸

New York, New York, United States

© Copyright 2025. All Rights Reserved by MedPath