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NCT04200157 Clinical Trial

Testing the Decoy Effect to Increase Tobacco Treatment Uptake

Tobacco Smoking Clinical Trial

Official title:
Testing the Decoy Effect to Increase Tobacco Treatment Uptake

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04200157
Other study ID # 18-00830
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 10, 2018
Est. completion date July 22, 2019

Study information
Verified date December 2019
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

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 information / eligibility
Status Completed
Enrollment 600
Est. completion date July 22, 2019
Est. primary completion date July 22, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Self-reported current tobacco use Exclusion Criteria: -

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Online survey
Subjects will complete a single survey that takes 5-10 minutes to complete

Locations
Country Name City State
United States NYU Langone Health - Translational Research Building New York New York

Sponsors (1)
Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of counseling calls chosen 6 months
Primary Number of weeks until quit date chosen 6 months
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