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Project DEDUCE: Digital Envirotyping to Develop Understanding of Cigarette Smoking and the Environment

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Duke University

Status and phase

Not yet enrolling
Phase 4

Conditions

Smoking

Treatments

Drug: transdermal nicotine replacement therapy

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT07089901
1R01DA062639 (U.S. NIH Grant/Contract)
Pro00117480

Details and patient eligibility

About

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.

Enrollment

600 estimated patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. 21 years of age or older;
  2. Smoke ≥ 10 cigarettes/day of a brand delivering 0.5 mg nicotine (FTC method);
  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

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.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

600 participants in 1 patient group

study group
Experimental group
Description:
All participants will receive transdermal nicotine replacement therapy.
Treatment:
Drug: transdermal nicotine replacement therapy

Trial contacts and locations

1

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Central trial contact

Francis J. McClernon, PhD; Angela Kirby, MS

Data sourced from clinicaltrials.gov

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