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OpenTrials
Completed

NCT Number: NCT03585231

Pilot Trial of the First Conversational Agent for Smoking Cessation (QuitBot)

Conversational agents (CAs) are computer-powered digital coaches designed to form long-term social-emotional connections with users through conversations. We have developed a CA for cigarette smoking cessation. In a pilot randomized trial (N = 415), we will compare the experimental messaging program (n = 155) with the standard of care national government smoking cessation messaging program (n = 157), and then we will compare immediate (n=51) versus delayed (n=51) access to the the experimental messaging program, to assess 12-week usability, receptivity, and preliminary cessation results in adults in western Washington State and nationally across the US who want to quit smoking.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fred Hutchinson Cancer Research Center

Seattle, Washington, 98109, United States

About this study

Cigarette smoking is the most preventable cause of cancer in the US, accounting for one-third of all cancer deaths. Within the Fred Hutchinson Center's western Washington State 13-county catchment area, there are enormous disparities in adult cigarette smoking rates. Our recently completed WebQuit website RCT for smoking cessation had low engagement and no personalization to users' needs. Fortunately, a potentially game-changing solution to the problems of engagement and lack of personalization provide a new direction for my research. Advances in machine learning, natural language processing, and cloud computing are making it possible to create and widely disseminate conversational agents (CAs), which are computer-powered digital coaches designed to form long-term social-emotional connections with users through conversations. We have developed a CA for cigarette smoking cessation. In a pilot randomized trial (N = 415), we will compare the experimental messaging program with the standard of care national government smoking cessation messaging program, and then we will compare immediate versus delayed access to the the experimental messaging program. Twelve-week usability, receptivity, and preliminary cessation results will provide critical and timely pilot data.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • age 18 or older
  • smokes at least five cigarettes daily for at least past 12 months
  • wants to quit cigarette smoking in the next 14 days
  • if concurrently using any other nicotine or tobacco products, wants to quit using them within the next 14days
  • resides in western Washington State (in the following counties: Clallam, Grays Harbor, Island, Jefferson, King, Kitsap, Mason, Pierce, San Juan, Skagit, Snohomish, Thurston, and Whatcom)
  • interested in learning skills to quit smoking
  • willing to be randomly assigned to either condition
  • has at least daily access to their own personal smartphone
  • has and uses both text messaging and Facebook Messenger on their smartphone
  • willing and able to read in English
  • not using other smoking cessation interventions (including apps or our other intervention studies).
  • willing to complete one 3-month follow-up survey
  • willing to provide email, phone, and mailing address.

Exclusion criteria

  • The exclusion criteria are opposite of the inclusion criteria listed above.

Treatment and study plan

Immediate access to novel messaging program intervention

Behavioral

The experimental arm includes an immediate intervention using a novel messaging program for smoking cessation.

Immediate access to standard of care messaging program intervention

Behavioral

The immediate control intervention uses a standard of care messaging program for smoking cessation.

Delayed access to novel novel messaging program intervention

Behavioral

The delayed control intervention uses the novel messaging program for smoking cessation.

Primary outcomes

  1. 30-day point prevalence abstinence

    Time frame: 3 months post randomization

    No smoking in the past 30 days, as reported 3 month post treatment.

Sponsors and collaborators

Lead sponsor

Fred Hutchinson Cancer Center

Other

Registry information

Official study title

Say "Hello" To Your Digital Coach: Development and Pilot Trial of the First Conversational Agent for Smoking Cessation

Acronym: QuitBot

Important dates

Study start
2018
Primary completion
2019
Study completion
2020
First posted
Jul 12, 2018
Registry last updated
Dec 8, 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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