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- Klinische Studie NCT07826884
Optimizing Chatbot Reminder Timing in a Chatbot Cessation Service: A Micro-Randomized Trial
16. September 2026 aktualisiert von: Prof. Wang Man-Ping, The University of Hong Kong
A Micro-Randomized Trial to Optimize the Timing of Weekly Chatbot Reminders for User Engagement in a Chatbot Cessation Service
The goal of this study is to learn whether the timing of weekly chatbot reminders affects user engagement with the chatbot cessation service.
Participants enrolled in the routine chatbot cessation service will be included in a micro-randomized trial.
The delivery timing of weekly reminders will be randomly assigned across different day types and times of day during the 12-week chatbot cessation service period.
The study will use routine chatbot system records to evaluate engagement after reminder delivery, including whether participants respond to the chatbot and how quickly they re-engage with the service.
Studienübersicht
Status
Noch keine Rekrutierung
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Sustained user engagement remains a challenge in digital smoking cessation interventions.
In this chatbot cessation service, routine weekly AI-generated reminders are used to encourage users to re-engage with chatbot-based smoking cessation support during the 12-week service period.
However, the optimal timing for delivering these reminders remains uncertain.
This study is an embedded micro-randomized trial conducted within the existing chatbot cessation service.
The aim of this study is to evaluate whether the timing of weekly chatbot reminders influences short-term user engagement and to identify optimal reminder delivery schedules.
Participants enrolled in the routine chatbot cessation service will be included in the micro-randomized trial through an opt-out approach.
The trial will not introduce any additional intervention components, measurements, or study visits beyond the existing chatbot cessation service and follow-up assessments.
Participation in the micro-randomized trial will only affect the timing of routine weekly reminders.
During the 12-week chatbot cessation service period, excluding the initial welcoming message, the delivery timing of 11 weekly reminders will be randomized across predefined day-type and time-of-day conditions.
Reminder strategy will remain unchanged.
The primary proximal outcome is meaningful engagement with the chatbot within 24 hours after reminder delivery, as recorded by the chatbot system.
Secondary outcomes include reply status, response latency, and meaningful engagement within 48 and 72 hours after reminder delivery.
Meaningful engagement is defined as user messages relevant to smoking cessaation.
The findings from this study will provide evidence to optimize the timing of routine chatbot reminders and inform future development of optimized reminder strategies and adaptive digital smoking cessation interventions.
Studientyp
Interventionell
Einschreibung (Geschätzt)
350
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Man Ping Wang
- Telefonnummer: +852 3917 6636
- E-Mail: mpwang@hku.hk
Studienorte
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-
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Hong Kong, Hongkong
- School of Nursing, The University of Hong Kong
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Kontakt:
- Man Ping Wang
- Telefonnummer: +852 3917 6636
- E-Mail: mpwang@hku.hk
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-
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Kind
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Nein
Beschreibung
Inclusion Criteria:
- Able to communicate in Chinese (Cantonese)
- Have access to or are willing to use WhatsApp to access the chatbot cessation service
- Used any tobacco in the past 30 days (including all types of tobacco products such as cigarette, shisha, electronic cigarettes, and heat-not-burn (HNB))
Exclusion Criteria:
- Have communication difficulties (either physical or cognitive) that prevent completion of the counselling and assessments
- Having queries irrelevant to tobacco control
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Versorgungsforschung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: Chatbot Cessation Service With Randomized Reminder Timing
Participants will receive the routine chatbot-based smoking cessation service for 12 weeks.
Within the service, the delivery timing of weekly chatbot reminders will be repeatedly randomized at weekly decision points across predefined day-type and time-of-day conditions using a micro-randomized trial design.
The reminder content and chatbot support provided to participants will remain consistent.
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The chatbot cessation service provides digital smoking cessation support through a chatbot platform.
Participants receive routine chatbot-based cessation support, including scheduled weekly AI-generated reminders during the 12-week service period.
Excluding the initial welcoming message, the timing of the remaining 11 weekly reminders will be repeatedly randomized at weekly decision points across predefined day-type and time-of-day conditions.
The randomized component is limited to reminder delivery timing.
All participants receive the same chatbot content and support.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Meaningful engagement with chatbot within 24 hours after reminder delivery
Zeitfenster: Within 24 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
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Meaningful engagement is defined as any reply regarding smoking cessation excluding emoji and simple message like "Hi" within 24 hours after receiving a randomized weekly reminder.
Engagement will be automatically recorded by the chatbot system.
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Within 24 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Any chatbot reply within 24 hours after reminder delivery
Zeitfenster: Within 24 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
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Whether participants provide any reply to the chatbot after receiving a randomized weekly reminder, as recorded by the chatbot system.
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Within 24 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
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Response latency after reminder delivery
Zeitfenster: Within 72 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
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The time interval between randomized reminder delivery and the participant's first reply to the chatbot within 72 hours after reminder delivery, as recorded by the chatbot system.
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Within 72 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
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Extended meaningful engagement with chatbot after reminder delivery
Zeitfenster: Within 48 and 72 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
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Meaningful engagement is defined as any reply regarding smoking cessation excluding emoji and simple message like "Hi" within 48 and 72 hours after receiving a randomized weekly reminder.
Engagement will be automatically recorded by the chatbot system.
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Within 48 and 72 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
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Mitarbeiter und Ermittler
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Sponsor
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Geschätzt)
28. September 2026
Primärer Abschluss (Geschätzt)
31. Oktober 2027
Studienabschluss (Geschätzt)
31. Dezember 2027
Studienanmeldedaten
Zuerst eingereicht
11. September 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
16. September 2026
Zuerst gepostet (Tatsächlich)
17. September 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
17. September 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
16. September 2026
Zuletzt verifiziert
1. September 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- Chat to Quit_MRT
Plan für individuelle Teilnehmerdaten (IPD)
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Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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