New chatbot aims to help native americans kick the habit
NCT ID NCT06697496
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is testing two remote programs—a chatbot app called QuitBot and a text messaging service—to help American Indian and Alaska Native adults quit smoking. About 772 participants will be randomly assigned to one of the programs. The goal is to see which approach works better for helping people stay smoke-free and reduce their risk of smoking-related cancers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- QuitBot chatbot and text messaging program
- What this could lead to
- If successful, this could provide an effective, culturally tailored digital tool to help American Indian and Alaska Native people quit smoking and lower their cancer risk.
- What could go wrong
- This is a behavioral intervention trial, not a drug or cure. Success depends on engagement, and results may not apply to other populations. The study is not yet recruiting.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 772 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Self-identifying as American Indian or Alaska Native, either alone or in combination with other races * Age 18 and older * Smoking combustible cigarettes daily in the past year * Interest in quitting smoking * Interest in learning skills to quit smoking * Willing to be randomly assigned * Have daily access to their own Android or iPhone smartphone * Ability to download a smartphone app * Ability to read English * Not currently (i.e., within past 30 days) using other smoking cessation interventions * No prior participation in our studies * No prior use of SFT * No household or family member participating * US residency for the next twelve months * Willingness to complete follow-up assessments at the 3-, 6-, and 12-month follow-ups * Providing email, phone number(s), and mailing address Exclusion Criteria: * The reverse of the inclusion criteria * Pregnant or breastfeeding * Use of other tobacco products (e.g., ceremonial use of tobacco, e-cigarettes) will be assessed but is not an exclusion criterion, as it would limit the study's generalizability
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Fred Hutch/University of Washington Cancer Consortium
Seattle, Washington, 98109, United States
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Other studies related to the condition(s) this trial covers.
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