Recruiting

Digital Envirotyping

Sponsor:

Duke University

Code:

NCT07089901

Conditions

Smoking

Eligibility Criteria

Sex: All

Age: 21+

Healthy Volunteers: Not accepted

Interventions

transdermal nicotine replacement therapy

Study Details

Brief summary:

Tobacco use is a chronic relapsing condition. That is, even with state-of-the-art treatment, >70% of smoking cessation attempts end in a return to regular smoking. Research demonstrates that everyday environments associated with smoking trigger craving for cigarettes, provoke smoking, and lead to relapse. However, despite this knowledge, understanding of environmental correlates of smoking has been limited by a reliance on self-report, leading to imprecise information about the physical environments in which people live. To overcome this challenge, the research team has pioneered the development of digital envirotyping, which uses digital tools (e.g., sensors, cameras, artificial intelligence) to efficiently and accurately characterize and categorize environments with the goal of identifying environmental markers of behavior and health. Foundational to the digital envirotyping research is computer vision (CV), a type of artificial intelligence (AI) that enables computer systems to recognize objects and scenes in digital images, mimicking how humans perceive and understand visual information. With CV researchers can extract detailed and accurate information (i.e., objects and location types) about the everyday environments of people who smoke (PWS) and relate that information to smoking behavior. After validating the use of CV, the researchers used CV to develop enviromarkers of relapse risk. Importantly, they identified a novel enviromarker in which people at greater risk for relapse when they quit are exposed to a more consistent level of environment-related smoking risk as they move between their smoking and nonsmoking environments.

Research is now needed to advance digital envirotyping and enviromarker development in the field of tobacco addiction. The study will recruit a diverse, national sample of n=500 adults who are interested in quitting smoking. For two weeks prior to quitting, they will undergo photoEMA in which they will take two pictures of their current environment when they smoke, and randomly 10 times per day resulting in >300,000 images total. Cessation will be supported by nicotine replacement therapy (i.e., nicotine patch). The primary clinical outcome will be days to relapse. Specific aims are to (1) further develop, refine, and validate methods for efficient digital envirotyping at scale, (2) leverage CV and AI approaches to develop enviromarkers of smoking relapse, and (3) conduct analyses to increase understanding of environmental smoking risk in women and individuals with low socioeconomic status.

Conditions

Smoking

Study ID

NCT07089901

Start date

May 6, 2026

Status verified date

May, 2026

Completion date

Mar 31, 2030

Anticipated

Primary completion date

Mar 31, 2030

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 21+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. 21 years of age or older;
2. Smoke ≥ 10 cigarettes/day
3. Smoking daily for ≥ 2 years, with a stable smoking pattern for the past 6 months;
4. Intention to quit smoking and set a target quit date in the next 1 month;
5. Have an iPhone or Android smartphone capable of running the photoEMA and iCO software
6. Positive Urine Cotinine Test

Exclusion Criteria:

1. Pregnant, breastfeeding, or planning to become pregnant during the course of the study;
2. Currently in smoking cessation treatment or current use of smoking cessation products;
3. Regular use (i.e. >9 days/month) of non-cigarette nicotine-containing products (e.g. cigarillos, e-cigarettes);
4. Anticipating major life changes (e.g. new job, birth of a child) during the course of the study;
5. Unstable medical conditions;
6. Contraindication for nicotine replacement therapy.

Study Design

Enrollment

600 participants

Anticipated

Intervention Model

Single group

Primary purpose

Other

Interventions and Outcome Measures

Arms

experimental: study group

All participants will receive transdermal nicotine replacement therapy.

Interventions

transdermal nicotine replacement therapy

All participants will receive transdermal nicotine replacement therapy (21 mg. patches)

Primary outcome measure

  • Average number of days to smoking relapse [ Time Frame: From quit date to 6-month follow-up (about 6.5 months) ]

Central Contacts and Locations

Central contacts

Locations

Duke University Medical Center

Recruiting

Durham, North Carolina, United States, 27706

Contacts

Laura E Van Althuis, MHA

9196684312

More Information

Sponsor

Duke University

Last update posted

Jul 23, 2026

Last verified

May, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Duke University on 2026-07-23.