Ecological Momentary Assessment of Smoking Triggers, Needs, and Cigarette Forgoing
spark Forgo
1 other identifier
interventional
45
0 countries
N/A
Brief Summary
This study will evaluate a smartphone-based program designed to support adults who smoke cigarettes. Participants will use the spark app to complete brief surveys during the day and a daily evening survey about their smoking urges, smoking, decisions not to smoke, and everyday experiences. Participants will also log cigarettes when they smoke. After some cigarette logs, participants will answer a few additional questions about their situation and feelings; after others, they will only log the cigarette. The study has three phases. In the first phase, participants will complete surveys and cigarette logs without receiving intervention messages. In the second phase, they will receive motivational messages at random times. In the third phase, message timing and content will be tailored using information collected during the earlier phases. The study will examine whether personalized motivational messages can help participants forgo smoking in daily life.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2026
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
September 15, 2026
CompletedStudy Start
First participant enrolled
September 20, 2026
CompletedFirst Posted
Study publicly available on registry
October 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2027
October 1, 2026
September 1, 2026
3 months
September 15, 2026
September 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Percentage of weekly smoking urge episodes in which smoking is forgone
Smoking forgoing will be assessed using study-specific ecological momentary assessment (EMA) item: "Since the last prompt (check-in or smoking report), have you \*chosen\* to skip any cigarettes that you normally would have smoked?" (yes/no). The outcome is the percentage of participant-reported smoking urge episodes per week. Higher percentages indicate more smoking forgoing.
During the 21-day study period
Number of cigarettes smoked per day
Cigarette smoking will be assessed using count of the participant-initiated cigarette-event logs. The outcome is the mean number of cigarettes smoked per participant per week during the study period.
During the 21-day study period
Secondary Outcomes (4)
Mean weekly momentary smoking urge/craving intensity score
During the 21-day study period
Weekly EMA adherence
Throughout the study (week 1, 2, and 3).
Smoking forgoing following motivational-message delivery
During the two bouts of 7-day Non-Adaptive EMI and Adaptive EMI phases of the 21-day study period.
Cigarette smoking following motivational-message delivery
During the two bouts of 7-day Non-Adaptive EMI and Adaptive EMI phases of the 21-day study period.
Study Arms (1)
Single Group (EMA/EMI sequence)
EXPERIMENTALAll participants complete three phases in sequence: an EMA Observation Phase with no intervention messages; a Non-Adaptive EMI Phase with randomly timed motivational messages; and an Adaptive EMI Phase with motivational messages timed and tailored using predictive models. Participants complete EMA and evening surveys throughout and may self-initiate cigarette-event logs.
Interventions
Smartphone-delivered motivational messages provided at randomly selected times during the Non-Adaptive EMI Phase. Message timing and content are not tailored using participant behavior, context, or assessment data.
Smartphone-delivered motivational messages provided during the Adaptive EMI Phase. Message timing is determined using predictive models developed from earlier study-phase data, and message content is adapted to the participant's estimated likelihood of successfully forgoing smoking in their current context.
Eligibility Criteria
You may qualify if:
- Age 21 years or older.
- Has smoked at least 100 cigarettes in their lifetime.
- Currently smokes cigarettes every day.
- Smokes 10 or fewer cigarettes per day.
- Owns a compatible smartphone with reliable internet access and is willing to install and use the \*spark\* study application.
- Able to read and understand English.
- Willing and able to complete smartphone-based assessments, self-initiated cigarette-event logs, and daily evening surveys for the study duration.
- Able and willing to provide informed consent.
You may not qualify if:
- Current use of electronic cigarettes or vaping products.
- Unable to provide informed consent.
- Does not have a compatible smartphone or reliable internet access.
- Unable to complete study procedures because of a cognitive, visual, motor, or other impairment not accommodated by the study procedures.
- Currently enrolled in another smoking-cessation intervention study that would conflict with study participation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Primary Investigator
Study Record Dates
First Submitted
September 15, 2026
First Posted
October 1, 2026
Study Start
September 20, 2026
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
September 1, 2027
Last Updated
October 1, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared because the intensive, time-stamped ecological momentary assessment data and potential passive smartphone data may create a risk of participant re-identification. Data will be retained and managed in accordance with the approved protocol, informed-consent materials, institutional policies, and applicable regulations.