- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07826884
Optimizing Chatbot Reminder Timing in a Chatbot Cessation Service: A Micro-Randomized Trial
16. september 2026 oppdatert av: 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.
Studieoversikt
Status
Har ikke rekruttert ennå
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
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.
Studietype
Intervensjonell
Registrering (Antatt)
350
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Man Ping Wang
- Telefonnummer: +852 3917 6636
- E-post: mpwang@hku.hk
Studiesteder
-
-
-
Hong Kong, Hong Kong
- School of Nursing, The University of Hong Kong
-
Ta kontakt med:
- Man Ping Wang
- Telefonnummer: +852 3917 6636
- E-post: mpwang@hku.hk
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Beskrivelse
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
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Helsetjenesteforskning
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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.
|
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.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Meaningful engagement with chatbot within 24 hours after reminder delivery
Tidsramme: Within 24 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
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.
|
Within 24 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Any chatbot reply within 24 hours after reminder delivery
Tidsramme: Within 24 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
Whether participants provide any reply to the chatbot after receiving a randomized weekly reminder, as recorded by the chatbot system.
|
Within 24 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
|
Response latency after reminder delivery
Tidsramme: Within 72 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
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.
|
Within 72 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
|
Extended meaningful engagement with chatbot after reminder delivery
Tidsramme: Within 48 and 72 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
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.
|
Within 48 and 72 hours after each randomized reminder delivery during the 12-week chatbot cessation service period
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
28. september 2026
Primær fullføring (Antatt)
31. oktober 2027
Studiet fullført (Antatt)
31. desember 2027
Datoer for studieregistrering
Først innsendt
11. september 2026
Først innsendt som oppfylte QC-kriteriene
16. september 2026
Først lagt ut (Faktiske)
17. september 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
17. september 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
16. september 2026
Sist bekreftet
1. september 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- Chat to Quit_MRT
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .