Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Smoking
  • Smoking, Cigarette
  • Smoking Tobacco
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Random assignment of retail environment (7-11, CVS, control [no store]) to visit every weekday during the 4-week intervention periodMasking: Single (Investigator)Masking Description: Investigator will not know the condition assignment of individual participants unless reassessment is triggered by the stopping rule.Primary Purpose: Other

Participation Requirements

Age
Between 18 years and 65 years
Gender
Both males and females

Description

Individual participation in this study will take place over a period of up to 5 months. During (approximately) the first 6 weeks, the participant will be asked to share their geolocation information, attend 3 in-person visits (2 of which involve getting fMRI brain scans), and complete short surveys ...

Individual participation in this study will take place over a period of up to 5 months. During (approximately) the first 6 weeks, the participant will be asked to share their geolocation information, attend 3 in-person visits (2 of which involve getting fMRI brain scans), and complete short surveys and repeated tasks (e.g., responding to EMA, using study-provided funds to make small purchases from a specified retail environment) in the weeks between visits. Approximately 3-months after the in-person participation in the study is complete, participants will receive a follow-up phone call during which a researcher will ask the participant to verbally answer brief survey questions.

Tracking Information

NCT #
NCT04279483
Collaborators
  • National Cancer Institute (NCI)
  • New York University
  • Stanford University
Investigators
Principal Investigator: Emily Falk, PhD University of Pennsylvania