NCT05825001

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
104

participants targeted

Target at P50-P75 for not_applicable

Timeline
5mo left

Started Sep 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Study Progress80%
Sep 2024Oct 2026

First Submitted

Initial submission to the registry

April 11, 2023

Completed
13 days until next milestone

First Posted

Study publicly available on registry

April 24, 2023

Completed
1.4 years until next milestone

Study Start

First participant enrolled

September 15, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Expected
Last Updated

February 5, 2026

Status Verified

February 1, 2026

Enrollment Period

1 year

First QC Date

April 11, 2023

Last Update Submit

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)

EXPERIMENTAL

Participants receive the active EFT stimulus and use the iCOquit Smokerlyzer carbon monoxide monitor on study.

Behavioral: Smoking Cessation InterventionOther: Medical Device Usage and Evaluation

Arm II (control EFT)

ACTIVE COMPARATOR

Participants receive the control EFT stimulus and use the iCOquit Smokerlyzer carbon monoxide monitor on study.

Behavioral: Smoking Cessation Intervention (control)Other: Medical Device Usage and Evaluation

Interventions

Receive active EFT stimulus

Also known as: Smoking and Tobacco Use Cessation Interventions
Arm 1 (active EFT)

Receive control EFT stimulus

Also known as: Smoking and Tobacco Use Cessation Interventions
Arm II (control EFT)

Use iCOquit Smokerlyzer carbon monoxide monitor

Arm 1 (active EFT)Arm II (control EFT)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Interventions

Smoking Devices

Intervention Hierarchy (Ancestors)

Manufactured MaterialsTechnology, Industry, and Agriculture

Study Officials

  • Christine Sheffer

    Roswell Park

    PRINCIPAL INVESTIGATOR

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

Locations