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Texting your way to quit smoking: telegram bot tested in heart patients
NCT ID NCT07230249
First seen Jun 27, 2026 · Last updated Jul 29, 2026 · Updated 2 times
Summary
This study tests whether a 6-month program delivered through the Telegram messaging app can help people stop smoking after a heart attack. 142 adult smokers who use Telegram will either get the chatbot support or standard advice. The goal is to see if more people quit with the chatbot's help.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Telegram-based behavioral support program
- What this could lead to
- If it works, this could provide a simple, scalable way to help heart attack survivors quit smoking, reducing their risk of future heart problems.
- What could go wrong
- This is a small, early-stage trial with only 142 people. The intervention relies on a messaging app, so it may not work for everyone, and results may not apply to non-Telegram users.
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 142 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2027
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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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Willing and able to provide written informed consent. * Age 18 years or older. * Hospitalization with a confirmed diagnosis of acute myocardial infarction (MI), including both ST-elevation MI (STEMI) and non-ST-elevation MI (NSTEMI). * Current smoker at the time of index MI: self-reported smoking of at least one cigarette per day in the month prior to hospitalization. * Regular user of the Telegram messenger application (app installed on a personal smartphone). * Possession of a smartphone with internet access and a valid phone number. * Ability and willingness to provide contact information for a close relative or cohabiting person who can verify smoking status at follow-up. Exclusion Criteria: * Smoking cessation more than 1 month prior to the index MI hospitalization. * Physical or cognitive impairment that prevents the use of a smartphone (e.g., severe visual/hearing impairment, inability to read or respond to messages). * Inability to read and understand the Russian language fluently. * Comorbid condition with a life expectancy of less than 1 year. * Active severe mental illness (e.g., psychosis, severe untreated depression) that would impede understanding of the protocol or adherence. * Unwillingness or inability to provide contact details for a close relative for outcome verification.
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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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Ulyanovsk Regional Clinical Hospital
Ulyanovsk, Ulyanovsk Oblast, 432000, Russia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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