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Completed

NCT Number: NCT04510077

SmartQuit Program for Smoking Cessation

This trial investigates how well a smartphone-based smoking cessation program called SmartQuit works to help patients stop smoking. SmartQuit is an smartphone application-based smoking cessation program that includes a defined program consisting of interactive evidence-based exercises for dealing more effectively with urges to smoke, a place to track desired behaviors, personalized plans for quitting, and a certificate of completion once the recommended program components are completed. SmartQuit may help patients quit smoking, lower healthcare costs and reduce premature tobacco-related deaths.

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Key information

Conditions

Cigarette Smoking-Related Carcinoma Tobacco-Related Carcinoma

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fred Hutch/University of Washington Cancer Consortium

Seattle, Washington, 98109, United States

About this study

OUTLINE:

Patients use the SmartQuit program to learn and practice skill modules as often as they wish over 6 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Smokes at least five cigarettes daily for at least past 12 months
  • Wants to quit in the next 30 days
  • Interested in learning skills to quit smoking
  • Resides in United States (US)
  • Has at least daily access to their own smartphone
  • Knows how to login and download a smartphone application from their smartphone
  • Willing and able to read in English
  • Not participating in other smoking cessation interventions (including our other intervention studies)
  • Must be an employee of a company who is participating in recruitment
  • Willing to complete one follow-up survey
  • Provide email, phone, and mailing address

Treatment and study plan

SmartQuit Smoking and Tobacco Cessation Program

Behavioral

Use SmartQuit program

Other names: 2Morrow, SmartQuit

Survey Administration

Other

Ancillary studies

Primary outcomes

  1. Number of participants with 7-day cigarette smoking cessation at 2 months.

    Time frame: At 2 month follow-up

    No smoking at all in the past 7 or more days (7-day point prevalence quit rate).

Secondary outcomes

  1. 24-hour point prevalence quit rate

    Time frame: At 2 month follow-up

  2. Change in number of cigarettes smoked per day

    Time frame: At 2 month follow-up

  3. Number of intentional 24-hour quit attempts

    Time frame: At 2 month follow-up

  4. Change in readiness to quit

    Time frame: At 2 month follow-up

    Differences in a participant's readiness to quit will be assessed by comparing their responses to the baseline survey readiness to quit questions with their responses to the 2 month follow-up survey

  5. Nicotine dependence level

    Time frame: At 2 month follow-up

    Participants will share their nicotine dependence level via survey at their 2 month follow-up

  6. Number of times logged into the application

    Time frame: At 2 month follow-up

    Will be assessed via 2 month follow-up survey

  7. Time spent on the application

    Time frame: At 2 month follow-up

    Will be assessed via 2 month follow-up survey

  8. Participant satisfaction with the application

    Time frame: At 2 month follow-up

    Will be assessed via 2 month follow-up survey

  9. Participant opinion of the usefulness of the application for quitting smoking

    Time frame: At 2 month follow-up

    Will be assessed via 2 month follow-up survey

Sponsors and collaborators

Lead sponsor

Fred Hutchinson Cancer Center

Other

Collaborators

  • Life Sciences Discovery Fund

Registry information

Official study title

Study of SmartQuit, a Smartphone-Based Smoking Cessation Program

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Aug 12, 2020
Registry last updated
Aug 12, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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