Actively Recruiting

Phase 2
Age: 18Years +
All Genders
Healthy Volunteers
ID06088498

Augmented Reality as an Adjunct to Quitline Counseling for Smoking Cessation

Led by H. Lee Moffitt Cancer Center and Research Institute · Updated on 2026-02-09

3600

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

H

H. Lee Moffitt Cancer Center and Research Institute

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating a smartphone application designed to reduce cravings to smoke as an additional tool alongside Tobacco Quitline treatment. The study aims to improve smoking abstinence by updating the app to be more engaging and user-friendly, and then testing its efficacy compared to quitline treatment alone. This is a Phase 2 randomized controlled trial sponsored by H. Lee Moffitt Cancer Center and Research Institute. Participants will be assigned to one of several groups. One group will receive usual care through the quitline, which includes cognitive behavioral therapy, support calls, and nicotine replacement therapy. Another group will use an updated smartphone app that tracks smoking urges and abstinence, with daily smoking extinction sessions involving multiple cues. Those in the app group who maintain 48 hours of abstinence will undergo additional extinction trials through the app. The app usage period lasts about five weeks. During the study, participants will complete assessments such as the System Usability Scale and user satisfaction surveys after one week, and tobacco abstinence status will be measured at six months. The study involves regular self-reporting of smoking urges and abstinence, with reminders to complete extinction sessions. Participants must own a smartphone that supports augmented reality and be willing to use the app. The total study participation includes follow-up visits and monitoring of smoking behavior and app usability.

CONDITIONS

Brief Title

App for Reducing Cravings to Smoke

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Over 18 years of age
  • Daily smokers who have quit within the past 3 months (Aim 1) or currently smoke at least 3 cigarettes per day for the past year (Aim 2)
  • Have a working telephone number
  • Own a smartphone that supports augmented reality and are willing to download the app
  • Can speak, read, and write in English
Not Eligible

You will not qualify if you...

  • Another household member is already enrolled in the study

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

App Update and User Satisfaction Evaluation

Duration - 1 week

Participants use an updated smartphone app designed to reduce cravings to smoke and provide feedback on usability and satisfaction.

1 baseline visit and 1 follow-up visit

Quitline Smoking Cessation Treatment

Duration - Up to 6 months

Participants receive quitline services including cognitive behavioral therapy, support calls, and nicotine replacement therapy to aid smoking cessation. Some participants also use a smartphone app to track smoking urges and abstinence.

Multiple phone calls and app usage as part of quitline program

Smoking Extinction via Smartphone App

Duration - 5 weeks

Participants who report 48 hours of abstinence use a smartphone app to complete daily smoking extinction sessions to reduce cravings.

Daily app sessions with 2-5 extinction sessions per day

Trial Site Locations

Total: 1 location

1

Moffitt Cancer Center

Tampa, Florida, United States, 33612

Actively Recruiting

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Research Team

C

Christine Vinci, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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Published Research Related To This Trial

Using augmented reality to deliver cue exposure treatment for smoking cessation: App usability findings and protocol for a randomized controlled trial.

Ranjita Poudel, Skye O Dougan, Helen Yates...

https://pubmed.ncbi.nlm.nih.gov/39880329