Testing the Decoy Effect to Increase Tobacco Treatment Uptake
- 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
- Self-reported current tobacco use
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description 7 Online survey Group assigned to the following answer combination: 1. 2 sessions (30 minutes) 2. 7 sessions (105 minutes) 5 Online survey Group assigned to the following answer combination: 1. 2 sessions (30 minutes) 2. 4 sessions (60 minutes) 1 Online survey Group assigned to the following answer combination: 1. 2 sessions 2. 4 sessions 3 Online survey Group assigned to the following answer combination: 1. 2 sessions 2. 7 sessions 9 Online survey Group assigned to the following answer combination: 1. 2 sessions (30 minutes) - 10% chance of quitting 2. 4 sessions (60 minutes) - 30% chance of quitting 11 Online survey Group assigned to the following answer combination: 1. 2 sessions (30 minutes) - 10% chance of quitting 2. 7 sessions (105 minutes) - 30% chance of quitting 4 Online survey Group assigned to the following answer combination: 1. 2 sessions 2. 7 sessions 3. 10 sessions 12 Online survey Group 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 2 Online survey Group assigned to the following answer combination: 1. 2 sessions 2. 4 sessions 3. 7 sessions 6 Online survey Group assigned to the following answer combination: 1. 2 sessions (30 minutes) 2. 4 sessions (60 minutes) 3. 7 sessions (105 minutes) 8 Online survey Group assigned to the following answer combination: 1. 2 sessions (30 minutes) 2. 7 sessions (105 minutes) 3. 10 sessions (150 minutes) 10 Online survey Group 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
Name Time Method Number of weeks until quit date chosen 6 months Number of counseling calls chosen 6 months
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
NYU Langone Health - Translational Research Building
🇺🇸New York, New York, United States