- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07826884
Optimizing Chatbot Reminder Timing in a Chatbot Cessation Service: A Micro-Randomized Trial
16 septembre 2026 mis à jour par: 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.
Aperçu de l'étude
Statut
Pas encore de recrutement
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Interventionnel
Inscription (Estimé)
350
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Man Ping Wang
- Numéro de téléphone: +852 3917 6636
- E-mail: mpwang@hku.hk
Lieux d'étude
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Hong Kong, Hong Kong
- School of Nursing, The University of Hong Kong
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Contact:
- Man Ping Wang
- Numéro de téléphone: +852 3917 6636
- E-mail: mpwang@hku.hk
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
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
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Recherche sur les services de santé
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: 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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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Meaningful engagement with chatbot within 24 hours after reminder delivery
Délai: 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
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Any chatbot reply within 24 hours after reminder delivery
Délai: 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
Délai: 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
Délai: 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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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
28 septembre 2026
Achèvement primaire (Estimé)
31 octobre 2027
Achèvement de l'étude (Estimé)
31 décembre 2027
Dates d'inscription aux études
Première soumission
11 septembre 2026
Première soumission répondant aux critères de contrôle qualité
16 septembre 2026
Première publication (Réel)
17 septembre 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
17 septembre 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
16 septembre 2026
Dernière vérification
1 septembre 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- Chat to Quit_MRT
Plan pour les données individuelles des participants (IPD)
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NON
Informations sur les médicaments et les dispositifs, documents d'étude
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Étudie un produit d'appareil réglementé par la FDA américaine
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