Evaluating the Episodic Future Thinking Intervention for Reducing Cigarette Consumption in Cigarette Smokers
Pilot Study of Episodic Future Thinking Among Cigarette Smokers
1 other identifier
interventional
104
1 country
1
Brief Summary
This clinical trial evaluates the effectiveness of active episodic future thinking (EFT) stimuli for reducing cigarette consumption in cigarette smokers. EFT is an innovative framing method shown to significantly activate brain regions involved in future thinking, planning, and other executive functions. Active EFT stimuli are positive events, unrelated to smoking, that participants anticipate, look forward to, and can vividly imagine happening up to 1 year in the future. Control EFT stimuli are positive past events, unrelated to smoking, that participants can vividly remember happening in the recent past. Active EFT stimuli may help reduce cigarette consumption among cigarette smokers by exposing them to personally relevant future oriented stimuli.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2024
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 11, 2023
CompletedFirst Posted
Study publicly available on registry
April 24, 2023
CompletedStudy Start
First participant enrolled
September 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2026
ExpectedFebruary 5, 2026
February 1, 2026
1 year
April 11, 2023
February 3, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Concentration of carbon monoxide on breath
Will be measured by Micro+Basic carbon monoxide monitor
From baseline up to 30 days
Secondary Outcomes (1)
Reduction in delay discounting rate
Up to 30 days
Study Arms (2)
Arm 1 (active EFT)
EXPERIMENTALParticipants receive the active EFT stimulus and use the iCOquit Smokerlyzer carbon monoxide monitor on study.
Arm II (control EFT)
ACTIVE COMPARATORParticipants receive the control EFT stimulus and use the iCOquit Smokerlyzer carbon monoxide monitor on study.
Interventions
Receive active EFT stimulus
Receive control EFT stimulus
Use iCOquit Smokerlyzer carbon monoxide monitor
Eligibility Criteria
You may qualify if:
- Smoke \>= 10 cigarettes daily
- \>32 on the Vividness of Visual Imagery Questionnaire (VVIQ)
- No regular use of other tobacco products
- In possession of a smartphone with text messaging capabilities
- Willing to quit smoking in the next 30 days
- Low socioeconomic status
- Veteran of the US armed services
You may not qualify if:
- Unable or unwilling to provide verbal consent
- Unable or unwilling to provide data to the research team
- Current use of nicotine replacement therapy, bupropion, or varenicline
- Use of drugs of abuse in the past 30 days
- Living in the same household as a participant already enrolled in this study
- Unable or unwilling to use nicotine patches
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Roswell Park Comprehensive Cancer Center
Buffalo, New York, 14263, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Christine Sheffer
Roswell Park
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 11, 2023
First Posted
April 24, 2023
Study Start
September 15, 2024
Primary Completion
October 1, 2025
Study Completion (Estimated)
October 1, 2026
Last Updated
February 5, 2026
Record last verified: 2026-02